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แนวทาง การตรวจวินิจฉัย และรักษาโรคมะเร็งเตานมสถาบันมะเร็ง PDF
แนวทาง การตรวจวินิจฉัย และรักษาโรคมะเร็งเตานมสถาบันมะเร็ง PDF
แนวทาง การตรวจวินิจฉัย และรักษาโรคมะเร็งเตานมสถาบันมะเร็ง PDF
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á¹Ç·Ò§¡ÒÃÃÑ¡ÉÒÁÐàÃç§àµÒ¹Á
· ÍÒ¡ÒäÅÓä´¡Í ¹·Õàè µÒ¹Á (Breast mass) 31
· ÊÒäѴËÅѧè ÍÍ¡·Ò§ËÑǹÁ (Nipple discharge) 34
· ÍÒ¡ÒÃà¨çººÃÔàdzàµÒ¹Á (Mastalgia) 36
· á¹Ç·Ò§¡ÒÃÃÑ¡ÉÒÁÐàÃç§àµÒ¹Áâ´Â¡ÒüҵѴ 38
á¹Ç·Ò§ÃѧÊÕÃ¡Ñ ÉÒã¹¼»Ù Ç ÂÁÐàÃç§àµÒ¹Á 44
á¹Ç·Ò§¡ÒÃÃÑ¡ÉÒàÊÃÔÁËÅѧ¼ÒµÑ´ã¹¼»Ù Ç ÂÁÐàÃç§àµÒ¹ÁÃÐÂÐáá 54
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· á¼¹ÀÙÁ¡Ô ÒÃàµÃÕÂÁáÅСÒÃÇÔ¹¨Ô ©Ñ·ҧ¾ÂÒ¸ÔÇ·Ô ÂÒ 83
· á¹Ç·Ò§»¯ÔºµÑ ¡Ô ÒÃʧµÃǨ·Ò§¾ÂÒ¸ÔÇ·Ô ÂÒ 88
· á¹Ç·Ò§¡ÒÃÍÒ¹à«ÅÅÇ·Ô ÂÒáÅÐÃÒ§ҹ¼ÅÊÔ§è à¨Òдٴ¨Ò¡àµÒ¹Á 91
ÍÂҧ໹Ãкº
· á¹Ç·Ò§¡ÒõѴªÔ¹
é à¹×Íé wide excision 97
· á¹Ç·Ò§¡ÒõÃǨà¹×Íé ¼ÒµÑ´·Ñ§é àµÒ¹Á (mastectomy) 98
Flow Chart
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹¨Ô ©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
2
DIAGNOSIS WORKUP RISK REDUCTION SURVEILLANCE
Biopsy was core Perform Ductal carcinoma Manage per
needle biopsy surgical in situ (DCIS) or appropriate
(less than surgical excision invasive cancer Guideline
biopsy)
19/2/2551, 20:58
surgical biopsy other cancer ´ÙË¹Ò 19
· Breast cancer risk
Counseling regarding reduction guidline
risk reduction ´ÙË¹Ò 31
· Breast cancer
screening and
diagnosis guideline
01-53_pc22.pmd
Ductal Carcinoma in Situ
3
DIAGNOSIS WORKUP PRIMARY TREATMENT
a
Margins greater than 10 mm are widely accepted as negative (but may be excessive and may lead to a less optimal cosmetic outcome).
Margins less than 1 mm are considered inadequate.
With pathologic margins between 1-10 mm, wider margins are generally associated with lower local recurrence rates. However, close surgical margins (< 1 mm) at
19/2/2551, 20:58
the fibroglandular boundary of the breast (chest wall or skin) do not mandate surgical re-excision but can be an indication for higher boost dose radiation to the involved
lumpectomy site. (category 2B)
b
Whole breast radiation therapy following lumpectomy reduces recurrence rates in DCIS by about 50%. Approximately half of the recurrences are invasive and half DCIS.
A number of factors determine that local recurrence risk; palpable mass, larger size, higher grade, close or involved margins, and age under 50 years. If the patient and
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
physician view the individual risk as "low", some patients may be treated by excision alone. All data evaluating the three local treatments show no differences in
patient survival.
3
01-53_pc22.pmd
4
4
DCIS POSTSURGICAL TREATMENT SURVEILLANCE/FOLLOW-UP
19/2/2551, 20:58
c
Available data suggest tamoxifen provides risk reduction in the ipsilateral breast treated with breast conservation and in the contralateral breast in patients with
mastectomy or breast conservation with ER-positive primary tumors. Since a survival advantage has not been demonstrated, individual consideration of risks and
benefits is important
01-53_pc22.pmd
Invasive Breast Cancer
5
CLINICAL STAGE WORKUP
19/2/2551, 20:58
Additional studies as directed by signs or symptoms:
T3, N1, M0 · Bone scan indicated if localized bone pain or elevated alkaline phosphatase
· Abdominal ± pelvis CT or US or MRI if elevated alkaline phosphatase, abnormal
liver function tests, abdominal symptoms, abnormal physical examination of
the abdomen or pelvis
· Chest imaging (if pulmonary symptoms are present)
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
6
LOCOREGIONAL TREATMENT OF CLINICAL STAGE I, IIA, OR IIB DISEASE OR T3, N1, M0
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staging (category 1) ± reconstruction
or
If T2 or T3 and fulfills criteria for breast Consider Preoperative Chemotherapy Guideline (Ë¹Ò 15)
conserving therapy except for size
d
Radiation therapy should follow chemotherapy when chemotherapy indicated.
01-53_pc22.pmd
Invasive Breast Cancer
7
LOCOREGIONAL TREATMENT OF CLINICAL STAGE I, IIA, OR IIB DISEASE OR T3, N1, M0
19/2/2551, 20:58
Negative axillary nodes
and tumor 5 cm and No radiation therapy
margins 1-2 mm
e
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
Radiation therapy should be given to the internal mammary lymph nodes that are clinically or pathologically positive, otherwise the treatment to the internal mammary
nodes is at the discretion of the treating radiation oncologist. CT treatment planning should be utilized in all cases where radiation therapy is delivered to the internal
7
8
HISTOLOGY HORMONE HER2 STATUS SYSTEMIC ADJUVANT TREATMENT
RECEPTOR STATUS
ER-positive
and/or
19/2/2551, 20:58
PgR positive
· Tubular See Systemic Adjuvant Treatment -
· Colloid ER-negative Favorable Histologies ˹Ò13
and
PgR-negative
f
This includes medullary and micropapillary subtypes.
01-53_pc22.pmd
Invasive Breast Cancer
9
SYSTEMIC ADJUVANT TREATMENT - HORMONE RECEPTOR POSITIVE - HER2 POSITIVE DISEASE
19/2/2551, 20:58
ipsilateral axillary lymph nodes) + trastuzumab (category 1)h
g
Mixed lobular and ductal carcinoma as well as metaplastic carcinoma should be graded based on the ductal component and treated based on this grading.
The metaplastic or mixed component does not alter prognosis.
h
Chemotherapy and endocrine therapy used as adjuvant therapy should be given sequentially with endocrine therapy following chemotherapy. The benefits of
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
chemotherapy and of endocrine therapy are additive. However, the absolute benefit from chemotherapy may be small. The decision to add chemotherapy to endocrine
therapy should be individualized, especially in those with a favorable prognosis where the incremental benefit of chemotherapy may be smaller.
9
Available data suggest sequential or concurrent endocrine therapy with radiation therapy is acceptable.
01-53_pc22.pmd
10
10
SYSTEMIC ADJUVANT TREATMENT - HORMONE RECEPTOR POSITIVE - HER2 NEGATIVE DISEASE
19/2/2551, 20:58
ipsilateral axillary lymph nodes) (category 1)
g
Mixed lobular and ductal carcinoma as well as metaplastic carcinoma should be graded based on the ductal component and treated based on this grading. The
metaplastic or mixed component does not alter prognosis.
h
Chemotherapy and endocrine therapy used as adjuvant therapy should be given sequentially with endocrine therapy following chemotherapy. The benefits of
chemotherapy and of endocrine therapy are additive. However, the absolute benefit from chemotherapy may be small. The decision to add chemotherapy to endocrine
therapy should be individualized, especially in those with a favorable prognosis where the incremental benefit of chemotherapy may be smaller. Available data suggest
sequential or concurrent endocrine therapy with radiation therapy is acceptable.
01-53_pc22.pmd
Invasive Breast Cancer
11
SYSTEMIC ADJUVANT TREATMENT - HORMONE RECEPTOR NEGATIVE - HER2 POSITIVE DISEASE
19/2/2551, 20:58
metastases > 2 mm to one or more + trastuzumab (category 1)
ipsilateral axillary lymph nodes)
g
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
Mixed lobular and ductal carcinoma as well as metaplastic carcinoma should be graded based on the ductal component and treated based on this grading. The
metaplastic or mixed component does not alter prognosis.
11
01-53_pc22.pmd
12
12
SYSTEMIC ADJUVANT TREATMENT - HORMONE RECEPTOR NEGATIVE - HER2 NEGATIVE DISEASE
19/2/2551, 20:58
metastases > 2 mm to one or more (category 1)
ipsilateral axillary lymph nodes)
g
Mixed lobular and ductal carcinoma as well as metaplastic carcinoma should be graded based on the ductal component and treated based on this grading. The
metaplastic or mixed component does not alter prognosis.
01-53_pc22.pmd
Invasive Breast Cancer
13
SYSTEMIC ADJUVANT TREATMENT - FAVORABLE HISTOLOGIES
19/2/2551, 20:58
and/or above
ER-negative Repeat determination of PgR-positive
and tumor estrogen/progesterone
PgR-negative receptor (ER/PgR) status ER-negative Treat as usual breast cancer
and histology (´ÙË¹Ò 11 áÅÐË¹Ò 12)
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
PgR-negative
13
01-53_pc22.pmd
14
14
Preoperative Chemotherapy Guideline
CLINICAL STAGE WORKUP
General workup including:
· History and physical
· CBC, platelets
Stage IIA · Liver function tests and alkaline phosphatase
T2, N0, M0 · Diagnostic bilateral mammogram, ultrasound as necessary
· Pathology review
· Determination of tumor ER/PgR status and HER2 status
Stage IIB
T2, N1, M0 Optional additional studies for breast imaging:
T3, N0, M0 · Breast MRI Preoperative
Chemotherapy
If clinical stage lllA (T3, N1, M0) consider: Ë¹Ò 15
Stage lllA · Bone scan (category 2B)
T3, N1, M0 · Abdominal ± pelvis CT or US or MRI
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
· Chest imaging
19/2/2551, 20:58
and Optional studies as directed by signs and symptoms:
· Bone scan indicated if localized bone pain or elevated alkaline phosphatase
Fulfills criteria for breast · Abdominal ± pelvis CT or US or MRI if elevated alkaline phosphatase,
conserving surgery abnormal liver function tests, abdominal symptoms, abnormal physical
except for tumor size examination of the abdomen or pelvis
· Chest imaging (if pulmonary symptoms are present)
· Consider fertility counseling if indicated
01-53_pc22.pmd
Invasive Breast Cancer
15
Preoperative Chemotherapy Guideline
PRIMARY TREATMENT
No response after
No response after 3-4 cycles
3-4 cycles or
or Progressive disease
Progressive disease MRM
Consider Partial response,
alternative lumpectomy not possi
chemotherapy
Preoperative Partial response,
chemotherapy lumpectomy not Complete response or ´Ù
possible partial response, Lumpectomy
lumpectomy possible Ë¹Ò 16
19/2/2551, 20:58
Partial response,
lumpectomy possible ´Ù
or Lumpectomy
Complete response Ë¹Ò 16
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
15
01-53_pc22.pmd
16
16
Preoperative Chemotherapy Guideline
LOCAL TREATMENT ADJUVANT TREATMENT
· Adjuvant radiation therapy post-mastectomy is
based on prechemotherapy tumor characteristics
and
Consider additional · Endocrine therapy if ER-positive and/or PgR-
MRM chemotherapy in the positiveh (category 1)
± reconstruction
context of a clinical trial · Complete up to one year of trastuzumab therapy
if HER2-positive (category 1). May be administered
concurrent with radiation therapy and with endocrine
therapy if indicated. ´Ù
Surveillance/
· Adjuvant radiation therapy post-lumpectomy based Follow-up
on prechemotherapy tumor characteristics ˹Ò19
and
Lumpectomy with Consider additional · Endocrine therapy if ER-positive and/or PgR-positiveh
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
19/2/2551, 20:58
staging · Complete up to one year of trastuzumab therapy if
HER2-positive (category 1). May be administered
concurrent with radiation therapy and with endocrine
therapy if indicated.
h
Chemotherapy and endocrine therapy used as adjuvant therapy should be given sequentially with endocrine therapy following chemotherapy. The benefits of
chemotherapy and of endocrine therapy are additive. However, the absolute benefit from chemotherapy may be small. The decision to add chemotherapy to endocrine
therapy should be individualized, especially in those with a favorable prognosis where the incremental benefit of chemotherapy may be smaller.
Available data suggest sequential or concurrent endocrine therapy with radiation therapy is acceptable.
01-53_pc22.pmd
Invasive Breast Cancer
LOCALLY ADVANCED INVASIVE BREAST CANCER (NON-INFLAMMATORY)
17
CLINICAL STAGE WORKUP
General workup including:
· History and physical
· CBC, platelets
Stage IIIA · Liver function tests and alkaline phosphatase
T0, N2, M0 · Diagnostic bilateral mammogram, ultrasound as necessary
T1, N2, M0 · Pathology review
T2, N2, M0 · Determination of tumor ER/PgR status and HER2 status
T3, N2, M0 Optional additional studies for breast imaging:
(Stage IIIA patients with T3, · Breast MRI ´Ù Preoperative
N1, M0 disease, ´ÙË¹Ò 13 If clinical stage lllA (T3, N1, M0) consider: Chemotherapy and
· Bone scan (category 2B) Locoregional
· Abdominal ± pelvis CT or US or MRI Treatment Ë¹Ò 18
· Chest imaging
Optional studies as directed by signs and symptoms:
Stage IIIB · Bone scan indicated if localized bone pain or elevated alkaline
T4, N0, M0 phosphatase
T4, N1, M0 · Abdominal ± pelvis CT or US or MRI if elevated alkaline
19/2/2551, 20:58
T4, N2, M0 phosphatase, abnormal liver function tests, abdominal symptoms,
abnormal physical
Stage lllC examination of the abdomen or pelvis
Any T, N3, M0 · Chest imaging (if pulmonary symptoms are present)
· FDG PET/CT scan (category 2B)
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
Any T, any N, M1
01-53_pc22.pmd
18
18
PREOPERATIVE CHEMOTHERAPY LOCOREGIONAL TREATMENT ADJUVANT TREATMENT
FOR LOCALLY ADVANCED
INVASIVE BREAST CANCER
(NON-INFLAMMATORY)
Total mastectomy + level l/ll axillary · Complete planned chemotherapy
dissection + radiation therapy to chest regimen course if not completed
wall and infraclavicular and preoperatively plus endocrine
Response supraclavicular nodes (plus internal treatment if ER-positive and/or
mammary nodes if involved, consider PgR-positive (sequential chemotherapy
internal mammary nodes if not clinically followed by endocrine therapy).
involved [category 3]) ± delayed breast · Complete up to one year of
reconstruction trastuzumab therapy if HER2-
or positive (category 1). May be ´Ù
Preoperative Consider lumpectomy + level l/ll axillary administered concurrent with Follow-up/
chemotherapy dissection + radiation therapy to breast radiation therapy and with Surveillance
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
19/2/2551, 20:58
involved)
19
SURVEILLANCE/FOLLOW-UP RECURRENT WORKUP
or
INITIAL WORKUP FOR STAGE IV DISEASE
19/2/2551, 20:58
adjuvant endocrine therapy. · Consider determination of tumor ER/PgR
· Evidence suggests that active lifestyle, and HER2 status if unknown, originally
achieving and maintaining an ideal body negative or not over-expressedb Systemic
weight (20-25 BMI) may lead to optimal disease
breast cancer outcomes.
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
19
01-53_pc22.pmd
20
20
SYSTEMIC TREATMENT OF RECURRENT OR STAGE IV DISEASE
Initial treatment with lumpectomy Total mastectomy + axillary lymph node staging if
+ radiation therapy level l/ll axillary dissection not previously done
Local only Initial treatment with mastectomy + level l / ll Surgical resection if possible
recurrence axillary dissection and prior radiation therapy
Initial treatment with mastectomy Surgical resection if possible + radiation therapy to
no prior radiation therapy chest wall and supraclavicular and infraclavicular
nodes Consider
Surgical resection if possible + radiation therapy if systemic
Axillary recurrence possible to chest wall, supraclavicular and therapy
Regional infraclavicular nodes, and axilla
only
or Radiation therapy if possible to chest wall and
Local and Supraclavicular recurrence supraclavicular and infraclavicular nodes
regional
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
19/2/2551, 20:58
internal mammary nodes
ER and/or PgR positive; HER2 negative
Bone disease present ER and/or PgR positive; HER2 positive
Systemic ER and PgR negative, or ER and/or PgR
disease positive and endocrine refractory; HER2
Bone disease not present negative
ER/PgR negative; HER2 positive
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á 21
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡ÃͧÁÐàÃç§àµÒ¹Á·ÕèàËÁÒÐÊÁÊÓËÃѺ»ÃÐà·Èä·Â
¨Ò¡¡ÒÃÈÖ¡ÉÒ¢ÍÁÙÅ·Ñé§ã¹áÅеҧ»ÃÐà·È¢Í§¤³Ð·Ó§Ò¹»ÃÐàÁԹ෤â¹âÅÂÕ¡ÒõÃǨÇÔ¹Ô¨©ÑÂ
ÁÐàÃç§àµÒ¹ÁÃÐÂÐáá¢Í§¡ÃÁ¡ÒÃᾷ¡ÃзÃǧÊÒ¸ÒóÊØ¢ » ¾.È. 2546(1) «Öè§ä´ÁÕ¡ÒûÃЪØÁÃдÁ
¤ÇÒÁ¤Ô´àËç¹¼ÙàªÕèÂǪÒÃÇÁ·Ñ駼ٷÕèà¡ÕèÂǢͧ·Ò§´Ò¹¹Õé ÊÃØ»ä´á¹Ç·Ò§ã¹¡ÒõÃǨ¤Ñ´¡ÃͧÁÐàÃç§àµÒ¹Á·Õè
àËÁÒÐÊÁÊÓËÃѺ»ÃÐà·Èä·Â ´Ñ§¹Õé
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1. ¡ÒõÃǨàµÒ¹Á´Çµ¹àͧ (breast self examination: BSE)
2. ¡ÒõÃǨàµÒ¹Áâ´Âá¾·ÂËÃ×ͺؤÅҡ÷ҧ¡ÒÃᾷ·äÕè ´ÃºÑ ¡Òý¡ÍºÃÁ (clinical breast exami-
nation: CBE)
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¢Íá¹Ð¹Ó (Recommendation)
1. Mass screening
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àµÒ¹Á·Õàè »¹áºº mass screening ÊÓËÃѺ»ÃÐà·Èä·Â ÊÃػ䴴§Ñ ¹Õé
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ÊÀÒÇÐÊØ¢ÀҾ㹢³Ð¹Ñ¹é áÅÐ ¡ÒÃÁÕªÇÕ µÔ ÍÂµÙ Í ä» (life expectancy)
¶Ö§áÁÇÒ ¨ÐÁÕ¡ÒÃÈÖ¡ÉÒÇÒ ¡ÒõÃǨàµÒ¹Á´Çµ¹àͧäÁä´Á¼Õ ŵ͡ÒÃÅ´ÍѵÃÒµÒ ᵡ¶ç Í× ÇÒ໹
ÇÔ¸¡Õ ÒõÃǨ¤Ñ´¡ÃͧÁÐàÃç§àµÒ¹Á·Õ»è ÃÐËÂÑ´·Õàè ËÁÒÐÊÁÊÓËÃѺ»ÃÐà·Èä·Â áÅÐ໹¡ÒÃÊÃÒ§¤ÇÒÁµÃÐ˹ѡ
ãË¡ºÑ ¼ËÙ Ô§ä·Â ãËÁ¤Õ ÇÒÁʹ㨡ѺÊØ¢ÀÒ¾¢Í§µ¹àͧ
2. Voluntary screening
2.1 ¼ËÙ Ô§·ÑÇè ä»
· ¼ËÙ Ô§·ÕÁè ÍÕ ÒÂص§Ñé áµ 20 »¢¹Öé ä»
¤ÇÃàÃÔèÁµÃǨàµÒ¹Á´Çµ¹àͧà´×͹ÅФÃÑé§ áÅФÇèеͧä´ÃѺ¡Òú͡¶Ö§»ÃÐ⪹áÅÐ
¢Í¨Ó¡Ñ´¢Í§¡ÒõÃǨàµÒ¹Á´Çµ¹àͧ ÃÇÁ·Ñé§ä´ÃѺ¡ÒÃÊ͹¡ÒõÃǨàµÒ¹Á´Çµ¹àͧ·Õè¶Ù¡ÇÔ¸Õ áÅФÇÃÁÕ
¡ÒõÃǨâ´Âá¾·ÂËÃ×Í ºØ¤Åҡ÷ҧ¡ÒÃᾷ·äÕè ´ÃºÑ ¡Òý¡ÍºÃÁ ÍÂÒ§¹Í·ء 3 »
· ¼Ë Ù Ô§·ÕÁè ÍÕ ÒÂØ 40 - 69 »¢¹Öé ä» áÅÐäÁÁÍÕ Ò¡ÒÃ
¹Í¡¨Ò¡¡ÒõÃǨàµÒ¹Á´Çµ¹àͧ໹»ÃШÓáÅÇ ¤ÇõÃǨâ´Âá¾·ÂËÃ×ͺؤÅҡ÷ҧ¡ÒÃ
ᾷ·äÕè ´ÃºÑ ¡Òý¡ÍºÃÁ ·Ø¡ 1 » áÅеÃǨ´ÇÂà¤Ã×Íè §¶ÒÂÀÒ¾ÃѧÊÕàµÒ¹Á (mammography) ·Ø¡ 1-2 » ÍÒ¨ãª
¡ÒõÃǨ ÍÑŵÃÒ«ÒÇ´ÃÇ Á´ÇÂ㹡ÅÁØ ·ÕÁè Õ Dense breast ¶ÒʶҹºÃÔ¡ÒÃÁÕ¤ÇÒÁ¾ÃÍÁ·Õ¨è еÃǨä´
¹Í¡¨Ò¡¹Õé¼ÙËÔ§â´Â·ÑèÇ令ÇÃä´ÃѺ¢ÍÁÙÅà¡ÕèÂǡѺ»ÃÐ⪹ ¤×Í ¡ÒõÃǨ¾ºÁÐàÃç§àµÒ¹Á
ã¹ÃÐÂÐáá ¢Í¨Ó¡Ñ´ã¹¡ÅÁØ ÊµÃÕ·ÁÕè Õ Dense breast áÅСÒÃá»Å¼Å¼Ô´¾ÅÒ´ 10-30% (ʶԵ¨Ô ҡʶҺѹ·ÑÇè âÅ¡)
áÅÐà¹×èͧ¨Ò¡à¹×éÍ àµÒ¹Á¢Í§ÊµÃÕä·ÂÁÕÅѡɳÐ໹ Dense breast ÍҨ㪡ÒõÃǨ ÍÑŵÃÒ«ÒÇ´ ÃÇÁ´Ç «Öè§
¨Ðãªã¹Ê¶ÒºÑ¹·ÕÁè ¤Õ ÇÒÁ¾ÃÍÁ¢Í§à¤Ã×Íè §Á×Í
v v v
á¹Ç·Ò§¡ÒÃãªà¤Ã×èͧ¶ÒÂÀÒ¾ÃѧÊÕàµÒ¹Á
(Mammography)
¤Ø³ÅѡɳТͧà¤Ã×èͧ¶ÒÂÀÒ¾ÃѧÊÕàµÒ¹Á
Mammographic Unit ·Õèä´ÁҵðҹÃѺÃͧãªä´·ÑèÇ仵ÒÁÁҵðҹÊҡŠહ ÂØâû ËÃ×Í ÊËÃÑ°
ÍàÁÃÔ¡Ò áÅÐÁÕà¤Ã×Íè §Á×Í·´Êͺ¤Ø³ÀÒ¾»ÃШÓà¤Ã×Íè §
ͧ¤»ÃСͺ¢Í§Ë¹Ç¶ÒÂÀÒ¾ÃѧÊÕàµÒ¹Á
· ʶҹ·Õè ãËàËÁÒÐÊÁ¡Ñºà¤Ã×Íè §Á×Í ¤ÇÃÁÔ´ªÔ´ áÅÐÁÕ¤ÇÒÁÊÐÍÒ´
· à¤Ã×Íè §Á×ÍʹѺʹعà¾ÔÁè àµÔÁ (·Õ¹è Ò ¨ÐÁÕÊÓËÃѺ¡ÒÃÇÔ¹¨Ô ©ÑÂ)
- à¤Ã×Íè §ÍÑŵÃÒ«ÒÇ´·ÁÕè ËÕ ÇÑ µÃǨª¹Ô´ high resolution ÁÒ¡¡ÇÒ 10 MHz ¢Ö¹é ä»
· ºØ¤ÅÒ¡Ã
1. ÃѧÊÕá¾·Â ·ÕÁè ¤Õ ³Ø ÊÁºÑµµÔ ÒÁ·Õ¡è Ó˹´
2. ¹Ñ¡ÃѧÊÕ¡ÒÃá¾·ÂËÃ×Íà¨Ò˹ҷÕÃè §Ñ ÊÕ¡ÒÃá¾·Â ·ÕÁè ¤Õ ³ Ø ÊÁºÑµµÔ ÒÁ·Õ¡è Ó˹´
3. à¨ÒË¹Ò·Õºè ¹Ñ ·Ö¡¢ÍÁÙÅáÅеԴµÍÊ×Íè ÊÒáѺ¼»Ù Ç Â
4. à¨Ò˹ҷÕÅè Ò §¿ÅÁ ¶ÒäÁä´ãª full-field digital mammography
á¹Ç·Ò§¡ÒäǺ¤ØÁ¤Ø³ÀÒ¾¢Í§¡ÒõÃǨÇÔ¹Ô¨©ÑÂàµÒ¹Áâ´Âà¤Ã×èͧ¶ÒÂÀÒ¾
ÃѧÊÕàµÒ¹Á (Guidelines for Mammography Quality Standard)
1. ºØ¤ÅÒ¡Ã (personal)
· ÃѧÊÕá¾·Â (radiologist)
¤Ø³ÊÁºÑµ·Ô ÇÑè ä»: ¨ºá¾·ÂÈÒʵú³ Ñ ±Ôµ áÅÐä´ÃºÑ ÇزºÔ µÑ ÃÃѧÊÕÇ·Ô ÂÒ ËÃ×ÍÇزºÔ µÑ ÃÃѧÊÕÇ¹Ô ¨Ô ©ÑÂ
¤Ø³ÊÁºÑµàÔ ©¾ÒÐ: 1. ä´ÃѺ¡Òý¡ÍºÃÁ ¡ÒÃÇÔ¹Ô¨©Ñ¡ÒõÃǨàµÒ¹Áâ´Âà¤Ã×èͧ¶ÒÂÀÒ¾ÃѧÊÕ
àµÒ¹Á ã¹âçàÃÕ¹ᾷÂËÃ×ÍʶҺѹ·Õèä´ÃѺ¡ÒÃÃѺÃͧÍÂÒ§¹Í 30
ªÑÇè âÁ§ ã¹¢³Ð·Õàè »¹á¾·Â»ÃШӺҹ
2. ¡Ã³ÕäÁä´ÃºÑ ¡Òý¡ÍºÃÁ¡ÒÃÇÔ¹¨Ô ©Ñ¡ÒõÃǨàµÒ¹Á â´Âà¤Ã×Íè §¶ÒÂÀÒ¾
ÃѧÊÕàµÒ¹Á ã¹¢³Ð໹ᾷ»ÃШӺҹ ËÃ×ÍäÁä´·Ó¡ÒÃÇÔ¹Ô¨©Ñ¡ÒÃ
µÃǨÀÒ¾ÃѧÊÕàµÒ¹ÁËÅѧ¨Ò¡¨º¡ÒÃÈÖ¡ÉÒà¡Ô¹ 3 » ¤Çüҹ¡ÒÃͺÃÁ
ËÅÑ¡ÊٵáÒÃÇÔ¹¨Ô ©Ñ¡ÒõÃǨÀÒ¾¶ÒÂÃѧÊÕàµÒ¹Áã¹âçàÃÕ¹ᾷÂËÃ×Í
ʶҺѹ·Õäè ´ÃºÑ ¡ÒÃÃѺÃͧÍÂÒ§¹Í 120 ªÑÇè âÁ§ ËÃ×ÍÁÕ»ÃÐʺ¡Òóã¹
¡ÒÃÍÒ¹á»Å¼Å ÀÒ¾¶ÒÂÃѧÊÕàµÒ¹ÁÍÂÒ§¹Í 240 ÃÒÂ
· ¹Ñ¡ÃѧÊÕ¡ÒÃá¾·Â ËÃ×Í à¨Ò˹ҷÕÃè §Ñ ÊÕà·¤¹Ô¤ (radiologic technologist)
¤Ø³ÊÁºÑµ·Ô ÇÑè ä»: ä´ÃºÑ 㺻ÃСͺâäÈÔÅ»¢Í§¹Ñ¡ÃѧÊÕ¡ÒÃá¾·Â
¤Ø³ÊÁºÑµàÔ ©¾ÒÐ: ä´ÃºÑ ¡Òý¡ÍºÃÁ¡ÒõÃǨàµÒ¹Áâ´Âà¤Ã×Íè §¶ÒÂÀÒ¾ÃѧÊÕàµÒ¹Áã¹Ê¶ÒºÑ¹
·Õäè ´ÃºÑ ¡ÒÃÃѺÃͧÍÂÒ§¹Í 40 ªÑÇè âÁ§
ÃÒÂÅÐàÍÕ´¢Í§à·¤¹Ô¤¡ÒõÃǨ
1. ¤ÇöÒ·ÒÁҵðҹ 2 ·Ò ã¹áµÅТҧ ä´á¡ craniocaudal áÅÐ medeolateral oblique views
ÃÇÁ¶Ö§¡ÒöÒÂÀÒ¾à¾ÔÁè àµÔÁ ·Ò੾Òеҧ æ 㹡óշ¾Õè ºÃÍÂâä·ÕÊè §ÊÑÂËÃ×ÍäÁª´Ñ ਹ
2. ã¹áµÅÐÀÒ¾¤ÇèÐÁÕ¢Í ÁÙÅà¡ÕÂè ǡѺ
- ª×Íè ¹ÒÁÊ¡ØÅ ÍÒÂØ áÅÐàÅ¢»ÃШӵÑǼ¶Ù ¡Ù µÃǨ
- Çѹ·Õ·è äÕè ´ÃºÑ ¡ÒõÃǨ
- ·Ò·Õãè ªã¹¡ÒõÃǨ áÅÐͧÈҢͧ¡ÒÃàÍÕ§ËÅÍ´¶ÒÂÀÒ¾
- kV & mAs
- à¤Ã×Íè §Á×Í·Õµè ÃǨáÅÐcassette ·Õµè ÃǨ¤ÇÃÃкتÍ×è ËÃ×ÍÃËÑʢͧ¹Ñ¡ÃѧÊÕà·¤¹Ô¤¼¶Ù Ò ÂÀÒ¾
· ¡ÒÃà¡çº¼Å¡ÒõÃǨ
¤ÇÃà¡çºÀÒ¾µ¹©ºÑºáÅмšÒõÃǨÍÂÒ§¹Í 5 » áÅеͧã˼ÅáÅÐÀÒ¾µ¹©ºÑºá¡¼»Ù Ç ÂËÒ¡
ÁÕ¡ÒÃÃͧ¢Í (´Ñ´á»Å§¨Ò¡ ACR Practice guideline for the performance of screening mammography )(5)
4. ¡ÒÃàµÃÕÂÁµÑǼ»Ù Ç Â
· ¡ÒÃàµÃÕÂÁµÑǼ»Ù Ç Â
- ´Ò¹¨Ôµã¨
¤ÇÃ͸ԺÒÂã˼»Ù Ç Âà¢Ò㨶֧¤ÇÒÁ¨Ó໹㹡Òô֧áÅС´·ÑºàµÒ¹Á¾ÃÍÁ·Ñ§é ¢Í¤ÇÒÁÃÇÁÁ×Í
´Ç¤ÇÒÁ¹ÁØ ¹ÇÅÊØÀÒ¾
- ´Ò¹ÃÒ§¡ÒÂ
1. ËÒÁ·ÒủáÅÐÂÒÃЧѺ¡ÅÔ¹è µÑÇ à¹×Íè §¨Ò¡ÁÕÊÇ ¹¼ÊÁ¢Í§ÊÒ÷շè ÓãˤÅÒ¾ÂÒ¸ÔÊÀÒ¾ä´
2. ¤ÇõÃǨã¹Çѹ·Õè 6 ¶Ö§ 7 ¹Ñº¨Ò¡Çѹáá¢Í§¡ÒÃÁÕ»ÃШÓà´×͹à¾×Íè ËÅÕ¡àÅÕÂè §âÍ¡ÒÊ·Õ¼è »Ù Ç Â
àÃÔÁè µÑ§é ¤ÃÃÀ áÅÐÅ´¤ÇÒÁá¹¹·Öº¢Í§àµÒ¹Á
3. ¤Çúѹ·Ö¡Çѹ·ÕèÁÕ»ÃШÓà´×͹¤ÃÑé§ÊØ´·Ò áÅШӹǹºØµÃ¢Í§¼ÙÁÒÃѺ¡ÒõÃǨ »ÃÐÇѵÔ
à¡ÕÂè ǡѺàµÒ¹Á હ âä¢Í§àµÒ¹Á ¡ÒüҵѴâäÁÐàÃç§àµÒ¹Á㹤Ãͺ¤ÃÑÇ à»¹µ¹
6. ¡Åä¡¡ÒûÃÐàÁÔ¹¼Å¤ÇÒÁ¾Í㨢ͧ¼ÙÃѺ¡ÒõÃǨáÅÐᾷ·ÕèʧµÃǨ
(Consumer complaint mechanism)
¤ÇÃÁÕÃкº¡ÒûÃÐàÁÔ¹¼Åà¡ÕèÂǡѺ¢Íº¡¾Ãͧ¢Í§¡ÒõÃǨ·ÕèÁռšÃзºµÍ¼Å¡ÒõÃǨÍÂÒ§
ÃÒÂáç હ ¤Ø³ÀÒ¾¢Í§ÀÒ¾äÁ´Õ ¡ÒÃÇÔ¹¨Ô ©Ñ¼Դ¾ÅÒ´ 㪺¤Ø Åҡ÷բè Ò´¤Ø³ÊÁºÑµÔ ¡ÒÃÃÒ§ҹ¼ÅªÒ ¤ÇÒÁ
à¨çº»Ç´ÍÂÒ§Ãعáç㹡ÒõÃǨ¢Í§¼ÃÙ ºÑ ¡ÒõÃǨ ໹µ¹ áÅзӡÒÃÃǺÃÇÁà¾×Íè ¹ÓÁÒ»ÃÐÁÇÅËÒ˹·Ò§
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Assessment Categories
a. ¡ÒûÃÐàÁÔ¹â´ÂãªáÁÁâÁá¡ÃÁÂѧäÁÊÁºÙó
Category 0
- ¨Ó໹µÍ§ÁÕ¡ÒöÒÂàÍ¡«àÃÂà¾ÔÁè àµÔÁ áÅÐ/ËÃ×ÍáÁÁâÁá¡ÃÁ·Õàè ¤Â·Ó¡Í¹Ë¹Ò¹Õàé ¾×Íè ãªà»ÃÕº
à·Õº
- ÁÕʧÔè µÃǨ¾º·Õ¨è Ó໹µÍ§ÁÕ¡ÒöÒÂàÍ¡«àÃÂà¾ÔÁè àµÔÁ ËÑǢ͹ըé Ð㪡óշàÕè »¹¡ÒõÃǨ¤Ñ´¡Ãͧ
à·Ò¹Ñ¹é (screening) ¡ÒöÒÂàÍ¡«àÃÂà¾ÔÁè àµÔÁÍÒ¨ÃÇÁ¶Ö§ ¡Òá´à¹×Íé àµÒ¹ÁáÅǶÒÂ੾ÒШش (spot compression)
¡ÒöÒÂÀÒ¾¢ÂÒ (magnification) ¡ÒöÒÂÀÒ¾áÁÁâÁá¡ÃÁ¾ÔàÈÉÍ×¹è æ áÅСÒÃ㪤Å×¹è àÊÕ§¤ÇÒÁ¶ÕÊè §Ù (ultra-
sound)
¶Ò¡ÒõÃǨ¾ºÊÔ§è ¼Ô´»¡µÔ·äÕè Á㪠benign finding ÍÒ¨¨Ó໹µÍ§ãª¡ÒÃà»ÃÕºà·Õº¡ÑºáÁÁâÁá¡ÃÁ
·Õàè ¤Â·Ó¡Í¹Ë¹Ò¹Õé ÃѧÊÕᾷ¨Ð໹¼»Ù ÃÐàÁÔ¹ÇÒÁÕ¤ÇÒÁ¨Ó໹㹡ÒõԴµÒÁáÁÁâÁá¡ÃÁà¡ÒÁÒà»ÃÕºà·Õº
ÁÒ¡¹ÍÂà¾Õ§㴠Category 0 ¨Ðãªã¹¡Ã³ÕµÍ§¡ÒÃáÁÁâÁá¡ÃÁà¡ÒÁÒà»ÃÕºà·ÕºáµÂѧäÁÊÒÁÒöËÒä´ã¹
¢³Ð¹Ñé¹
b. ¡ÒûÃÐàÁÔ¹â´ÂãªáÁÁâÁá¡ÃÁÊÁºÙó¤Ãº¶Ç¹ - Final categories
Category 1
Negative
äÁ¾ºÊÔ§è ¼Ô´»¡µÔã´àÅ àµÒ¹ÁÊÁ´Øšѹ·Ñ§é 2 ¢Ò§ äÁÁ¡Õ Í ¹à¹×Íé (mass), ¡ÒúԴàºÕÂé Ǣͧà¹×Íé àµÒ¹Á
(architectural distortion) ËÃ×ÍËÔ¹»Ù¹
Category 2
ÊÔ§è µÃǨ¾ºäÁãªÁÐàÃç§ (benign finding) àËÁ×͹ category 1 Âѧ¨Ñ´à»¹¡ÒûÃÐàÁÔ¹¡ÅÁØ "»¡µÔ"
áµ¼áÙ »Å¼ÅµÍ§¡ÒúÃÃÂÒÂÊÔ§è µÃǨ¾º·Õäè ÁãªÁÐàÃç§ ¡ÅÁØ µÍ仹ÕÊé ÒÁÒöºÍ¡ä´ÇÒ äÁãªÁÐàÃç§ÍÂҧṹ͹
ä´á¡ fibroadenoma ·Õè½ÍÁÕËÔ¹»Ù¹¨Ñº, ¡ÅØÁËÔ¹»Ù¹ã¹ secretory disease, ¡ÅØÁ¾ÂÒ¸ÔÊÀÒ¾·ÕèÁÕä¢Áѹ໹
Êǹ»ÃСͺ હ oil cyst, lipoma, galactocele áÅÐ hamartoma ÃÇÁ¶Ö§ µÍÁ¹éÓàËÅ×ͧã¹àµÒ¹Á (intramammary
lymph node),ËÔ¹»Ù¹¢Í§àʹàÅ×Í´ã¹àµÒ¹Á, ÇÑÊ´ØàÊÃÔÁàµÒ¹Á ËÃ×Í¡ÒúԴàºÕÂé Ǣͧà¹×Íé àµÒ¹Á·Õàè ¡Ô´¨Ò¡¡ÒüҵѴ
·Ñé§ Category 1 áÅÐ 2 º§ªÕéÇÒäÁÁÕÅѡɳТͧÁÐàÃç§àµÒ¹Á»ÃÒ¡®ã¹áÁÁâÁá¡ÃÁ ¤ÇÒÁᵡ
µÒ§¤×Íã¹ Category 2 ¨ÐÁÕ¡ÒúÃÃÂÒ¶֧ÊÔ§è ·Õµè ÃǨ¾º (benign finding) áµ Category 1 ¨ÐäÁÁ¡Õ ÒúÃÃÂÒ ´Ñ§¡ÅÒÇ
Category 3
ÍÒ¨¨Ð໹ benign finding
- ã˵´Ô µÒÁ¼Å¡ÒõÃǨã¹ÃÐÂÐÊѹé
ÊÔ§è ¼Ô´»¡µÔ·µÕè ÃǨ¾º¨ÐÁÕâÍ¡ÒÊ໹ÁÐàÃç§àµÒ¹Á¹Í¡ÇÒ 2 % áÅФҴÇÒ¨ÐäÁÁ¡Õ ÒÃà»ÅÕÂè ¹
á»Å§ã¹ªÇ§·Õµè ´Ô µÒÁ¼Å
ÁÕ¡ÒÃÈÖ¡ÉÒ·ÕèÂ×¹Âѹ¤ÇÒÁ»ÅÍ´ÀÑÂáÅлÃÐÊÔ·¸Ô¼Å¢Í§¡ÒõԴµÒÁ¼Å¡ÒõÃǨã¹ÃÐÂÐÊÑé¹
(initial short- term follow-up) ã¹¼»Ù Ç Â¡ÅÁØ ¹Õé
Êǹã˼ٻÇÂ㹡ÅØÁ¹Õé¨ÐµÔ´µÒÁ¼ÅÃÐÂÐÊÑé¹ 6 à´×͹ ã¹ 1 » áÅзء 1 » ¨¹¤Ãº 2 » à¾×èÍ
Â×¹ÂѹÇÒ¤ÇÒÁ¼Ô´»¡µÔ¹¹Ñé ¤§·Õè ¨Ö§à»ÅÕÂè ¹à»¹ Category 2
Category 4
¤ÇÒÁ¼Ô´»¡µÔ·¾Õè ºÊ§ÊÑÂÇÒÍҨ໹ÁÐàÃç§ (suspicious abnormality)
- ¤ÇÃä´ÃºÑ ¡ÒõÃǨªÔ¹é à¹×Íé
ËÑǢ͹ըé ÐÃÇÁÊÔ§è ¼Ô´»¡µÔ·´Õè ¹Ù Ò ¡Ñ§ÇÅ¡ÇÒ Category 3 áµäÁàËÁ×͹ÅѡɳÐ੾ÒТͧÁÐàÃç§
Category 5
ʧÊÑÂÍÂÒ§ÂÔ§è ÇÒ¨Ð໹ÁÐàÃç§ (highly suspicious)
- ¨Ó໹µÍ§ä´ÃºÑ ¡ÒõÃǨªÔ¹é à¹×Íé ¤ÇÒÁ¼Ô´»¡µÔ·µÕè ÃǨ¾ºã¹¡ÅÁØ ¹ÕÁé âÕ Í¡ÒÊÊÙ§ÁÒ¡·Õ¨è Ð໹
ÁÐàÃç§ (> 95 %) ¤ÇÃÁÕ¡ÒôÓà¹Ô¹¡Ò÷Õàè ËÁÒÐÊÁµÍä»
Category 6
·ÃÒº¼ÅªÔ¹é à¹×Íé áÅÇÇÒ໹ÁÐàÃç§
- ¤ÇÃÁÕ¡ÒôÓà¹Ô¹¡Ò÷Õàè ËÁÒÐÊÁµÍä»
ËÑǢ͹Õãé ªÊÓËÃѺ¤ÇÒÁ¼Ô´»¡µÔ·àÕè Ëç¹ã¹áÁÁâÁá¡ÃÁ â´ÂÁÕ¡ÒõѴªÔ¹é à¹×Íé ¾Ôʨ٠¹¡Í ¹Ë¹Ò
¹Õáé ÅÇÇÒ໹ÁÐàÃç§ áµÁÒµÃǨáÁÁâÁá¡ÃÁà¾×Íè ´ÙÇÒ ÁÕÁÐàÃç§à¾Õ§µÓá˹§à´ÕÂÇ·Õäè ´ÃºÑ ¡ÒþÔʨ٠¹ª¹Ôé à¹×Íé áÅǨÐ
ä´ÇҧἹ¡ÒÃÃÑ¡ÉÒä´àËÁÒÐÊÁ ¶Ò¾º¤ÇÒÁ¼Ô´»¡µÔ·ÕèÍ×蹵ͧ»ÃÐàÁԹ仵ÒÁ¤ÇÒÁ¼Ô´»¡µÔ¹Ñé¹æ ÇÒÁÕ¤ÇÒÁ
ʧÊÑ¡ÒÃ໹ÁÐàÃç§ÁÒ¡¹ÍÂà¾Õ§ã´
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Ø ÀÒ¾´Õ·ÊÕè ´Ø ´Ç»ÃÔÁÒ³ÃѧÊÕ·àÕè ËÁÒÐÊÁ·ÕÊè ´Ø
- à¾×Íè ãËä´ÀÒ¾¶ÒÂÃѧÊÕàµÒ¹Á·ÕÊè ÒÁÒöµÃǨËÒÃÍÂâä¢Í§àµÒ¹Áä´ÅÐàÍÕ´¶Õ¶è Ç ¹·ÕÊè ´Ø
- à¾×Íè ËÅÕ¡àÅÕÂè §¤ÇÒÁ¼Ô´¾ÅÒ´ ÍѹÍÒ¨à¡Ô´¨Ò¡¡ÒÃÇÔ¹¨Ô ©ÑÂâä´ÇÂÀÒ¾¶ÒÂÃѧÊÕàµÒ¹ÁãËä´ÁÒ¡·ÕÊè ´Ø
˹ҷÕáè ÅеÒÃÒ§àÇÅÒ
· ÊÓËÃѺà¤Ã×Íè § Mammography Ẻ screen-film
¹Ñ¡ÃѧÊÕà·¤¹Ô¤ÁÕ˹ҷÕè 11 »ÃСÒà µÒÁµÒÃÒ§àÇÅÒµÍ仹Õé
¤ÇÒÁ¶ÕèµèÓÊØ´
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¢Í§¡Òû¯ÔºµÑ Ô
1. ·Ó¤ÇÒÁÊÐÍÒ´ËͧÁ×´ ·Ø¡Çѹ
2. ¤Çº¤ØÁ¤Ø³ÀÒ¾¡ÒÃÅÒ§¿ÅÁ ·Ø¡Çѹ
3. ·Ó¤ÇÒÁÊÐÍÒ´¤ÒÊà«· - Ê¡ÃÕ¹ ÊÑ»´ÒËÅФÃѧé
4. µÃǨÊͺÊÀÒÇСÒÃÍÒ¹¿ÅÁ ·Ó¤ÇÒÁÊÐÍÒ´µäÙ ¿Êͧ¿ÅÁ áÅÐáǹ¢ÂÒ ÊÑ»´ÒËÅФÃѧé
·Õãè ªã¹¡ÒôٿŠÁ
5. ¤Çº¤ØÁ¤Ø³ÀÒ¾â´ÂãªË¹Ø ¨ÓÅͧàµÒ¹Á à´×͹ÅФÃѧé
6. µÃǨÊͺÊÀÒ¾à¤Ã×Íè §´ÇÂµÒ à´×͹ÅФÃѧé
7. ÇÔà¤ÃÒÐË굄 ÃÒ¡ÒöÒ¿ÅÁ «éÓ 3 à´×͹¤Ãѧé
8. µÃǨÊͺ»ÃÔÁÒ³µ¡¤Ò§¢Í§äÎ⻺¹¿ÅÁ 3 à´×͹¤Ãѧé
9. µÃǨÊͺÃдѺËÁÍ¡¤Çѹ (fog) ¢Í§ËͧÁ×´ 6 à´×͹¤Ãѧé
10. µÃǨÊͺ¤ÇÒÁṺªÔ´¢Í§Ê¡ÃÕ¹áÅпÅÁ 6 à´×͹¤Ãѧé
11. µÃǨÊͺáç¡´¢Í§á¼¹¡´àµÒ¹Á 6 à´×͹¤Ãѧé
12. 㹡óշ¨Õè еͧÁÕ¡ÒÃ·Ó breast intervention ¨ÐµÍ§µÃǨÊͺ¤ÇÒÁáÁ¹ÂÓ ·Ø¡¤ÃÑ§é ¡Í¹¡Ò÷Ó
¢Í§à¤Ã×Íè §¶ÒÂÃѧÊÕÃкº stereotaxis
References
1. ¡ÒûÃÐàÁԹ෤â¹âÅÂÕ¡ÒõÃǨÇÔ¹¨Ô ©ÑÂÁÐàÃç§àµÒ¹Áã¹ÃÐÂÐàÃÔÁè áá·Õàè ËÁÒÐÊÁÊÓËÃѺ»ÃÐà·Èä·Â. ¡ÃÁ¡ÒÃá¾·Â ¡ÃзÃǧ ÊÒ¸ÒóÊØ¢.
µØÅÒ¤Á 2546.
2. Lee CH, Dershaw D, Kopan D, Evan P, Monsees B, Monticciolo D, et al. Breast Cancer Screening with Imaging: Recommendations
from the Society of Breast Imaging and the ACR on the Use of Mammography, Breast MRI, Breast Ultrasound, and Other Technologies
for the Detection of Clinically Occult Breast Cancer. JACR 2010;7:18-27.
3. ÊÁ㨠ªÒÇÔàÈÉ, ÊØàÁ¸ ÃÔ¹ÊØç¤Ç§È, ÊÁà¡ÕÂÃµÔ â¾¸ÔÊѵ áÅФ³Ð. á¹Ç·Ò§¡ÒÃãªà¤Ã×èͧ¶ÒÂÀÒ¾ÃѧÊÕàµÒ¹Á (Mammography)
㹡ÒõÃǨÇÔ¹¨Ô ©ÑÂÁÐàÃç§àµÒ¹Á. ÇÒÃÊÒáÃÁ¡ÒÃá¾·Â ¡ÃзÃǧÊÒ¸ÒóÊØ¢. 2545; 27: 454-462.
4. American College of Radiology (ACR) Breast Imaging Reporting and Data System (BIRADSTM) Forth Edition. Reston (VA):
American College of Radiology, 2003.
5. ACR Practice Guideline for the Performance of Screening Mammography American College of Radiology. Revised 2008. Available
from: URL http://www.acr.org/departments/stand_accred/standards/pdf/screening_mammography. pdf. Accessed on February 22nd,
2011.
v v v
á¹Ç·Ò§¡ÒõÃǨÇÔ¹Ô¨©ÑÂ
áÅÐÃÑ¡ÉÒÁÐàÃç§àµÒ¹Áâ´Â¡ÒüҵѴ
á¹Ç·Ò§¡ÒõÃǨÇÔ¹Ô¨©ÑÂâäàµÒ¹Á·Õ辺ºÍÂ
· ÍÒ¡ÒäÅÓä´¡Í ¹·Õàè µÒ¹Á (Breast mass)
· ÊÒäѴËÅÑè§ÍÍ¡·Ò§ËÑǹÁ (Nipple discharge)
· ÍÒ¡ÒÃà¨çººÃÔàdzàµÒ¹Á (Mastalgia)
á¹Ç·Ò§¡ÒÃÃÑ¡ÉÒÁÐàÃç§àµÒ¹Áâ´Â¡ÒüҵѴ
· á¹Ç·Ò§¡ÒÃÃÑ¡ÉÒÁÐàÃç§àµÒ¹Áâ´Â¡ÒüҵѴ
31
< 35 yr; ultrasound**
³ 35 yr, Mammogram + ultrasound
19/2/2551, 20:58
- Lobular carcinoma in situ
- Lobular neoplasia
Recurrent - Radial scar
* Triple
- Phyllodes
Non recurrent - Mucocele lesion
** ¢Ö¹
é ¡Ñº´ØžԹ¨Ô ¢Í§á¾·Â·¼µÙ ÃǨÃÑ¡ÉÒ
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
*** 㹡óշ¼Õè »Ù Ç ÂÍÒÂØ¹Í Â¡ÇÒ 25 »¡Í ¹¢¹Ò´àÅç¡ÁÕÅ¡Ñ É³Ð benign - Papillary lesion
ÍÒ¨ãË¡ÒôÙáÅâ´Â¡ÒõԴµÒÁµÒÁ¤ÇÒÁàËÁÒÐÊÁ ·Ø¡ 3-6 à´×͹
Routine screening Hx = history - Sclerosing adenosis
31
Breast mass
á¹Ç·Ò§¡ÒôÙáż»Ù Ç Â·ÕÁè Ò´ÇÂÍÒ¡ÒäÅÓä´¡Í ¹·Õàè µÒ¹Á ËÅѧ¨Ò¡¡Òëѡ»ÃÐÇѵáÔ ÅеÃǨÃÒ§¡ÒÂ
Â×¹ÂѹÇÒÁÕ¡Í ¹·Õàè µÒ¹Á¨ÃÔ§ ÍÒ¨á¹Ð¹ÓãË·Ó ultrasound àµÒ¹Áã¹¼ËÙ Ô§ÍÒÂØ¹Í Â¡ÇÒ 35 » ÊÓËÃѺ¼ËÙ Ô§ÍÒÂØ
35 » ¢Ö¹é ä» ÍÒ¨á¹Ð¹ÓãË·Ó mammogram ÃÇÁ´Ç â´ÂãËÍÂãÙ ¹´ØžԹ¨Ô ¢Í§á¾·Â¼ãÙ Ë¡ÒÃÃÑ¡ÉÒ à¹×Íè §¨Ò¡
¡Ò÷ÓáÁÁâÁá¡ÃÁ áÅÐËÃ×ÍÍÑŵÃÒ«ÒÇ´ ÁÕâÍ¡ÒÊà¡Ô´¼ÅźÅÇ§ä´ (false negative ) 15 %(1)
Cystic mass
· ¡Ã³Õ simple cyst á¹Ð¹ÓÇÒÊÒÁÒöãªÇÔ¸Õ¡ÒõÃǨµÔ´µÒÁä´ ËÃ×Í·Ó needle aspiration ¶Ò¢Í§
àËÅÇ·Õäè ´äÁÁÅÕ ¡Ñ ɳРbloody fluid áÅС͹ÂغËÁ´ á¹Ð¹ÓãË·Ó¡ÒõÃǨµÔ´µÒÁã¹ÍÕ¡ 6-8 ÊÑ»´ÒË ¶ÒäÁÁÕ
¡ÒáÅѺ໹«éÓ ÊÒÁÒö·ÓµÒÁ screening program »¡µÔä´
· ¶ÒÁÕÅѡɳРbloody fluid ËÃ×͡͹ÂغäÁËÁ´ ËÃ×ÍÁÕ¡ÒáÅѺ໹«éӢͧ¡Í¹ã¹ 6-8 ÊÑ»´ÒË
á¹Ð¹ÓãË·Ó¡ÒÃʧµÃǨµÍà¾×Íè ãËä´ tissue diagnosis
Solid mass
· àÁ×Íè µÃǨàµÒ¹Á¾º solid mass á¹Ð¹Óã˵ÃǨªÔ¹é à¹×Íé ´ÇÂÇÔ¸Õ fine needle aspiration(2, 3) ËÃ×Í core
needle biopsy ËÃ×Í excision biopsy
· ¡Ã³Õ·Ó triple assessment ´Ç clinical examination, imaging áÅÐ FNA ÁռšÒõÃǨ´Ñ§¹Õé
1. Benign ·Ñ§é ËÁ´ á¹Ð¹ÓÇÒÊÒÁÒöÃÑ¡ÉÒ´Ç¡ÒõԴµÒÁä´ ¶Ò¡Í¹ÁÕ¢¹Ò´àÅç¡¡ÇÒ 2 ૹµÔàÁµÃ
¡ÒõÃǨµÔ´µÒÁá¹Ð¹Óã˵ÃǨàµÒ¹Á ·Ø¡ 6 à´×͹ ໹àÇÅÒ 2 » ¶ÒÁÕ¢Í Ê§ÊѨҡÍÒ¡Ò÷ҧ¤ÅÔ¹¡Ô á¹Ð¹Ó·Ó
core needle biopsy ËÃ×Í excision áÅжҡ͹ÁÕ¢¹Ò´ãË¡ÇÒ 2-3 «Á.á¹Ð¹Ó·Óexcision
2. Malignant ·Ñ§é ËÁ´ ÊÒÁÒöãË¡ÒÃÇÔ¹¨Ô ©ÑÂáÅÐÃÑ¡ÉÒµÒÁá¹Ç·Ò§¡ÒÃÃÑ¡ÉÒÁÐàÃç§àµÒ¹Áä´
3. äÁÊÍ´¤Åͧ¡Ñ¹ á¹Ð¹ÓãËàÍÒªÔ¹é à¹×Íé µÃǨà¾ÔÁè àµÔÁ à¾×Íè Â×¹Âѹ¡ÒÃÇÔ¹¨Ô ©ÑÂ
· á¹Ð¹Ó·Ó excision ¡Í¹ 㹡óÕ
1. ¼Å core biopsy ໹(4-7)
- Atypical ductal hyperplasia
- Atypical lobular hyperplasia
- Lobular carcinoma in situ
- Lobular neoplasia
- Radial scar
- Phyllodes
- Mucocele lesion
- Papillary lesion
- Sclerosing adenosis
References
1. Kerlikowske K, Smith-Bindman R, Ljung BM, Grady D. Evaluation of abnormal mammography results and palpable breast abnormalities.
Ann Intern Med. 2003 Aug 19;139(4):274-84.
2. Wanebo HJ, Feldman PS, Wilhelm MC, Covell JL, Binns RL. Fine needle aspiration cytology in lieu of open biopsy in management of
primary breast cancer. Ann Surg. 1984 May;199(5):569-79.
3. Rimsten A, Stenkvist B, Johanson H, Lindgren A. The diagnostic accuracy of palpation and fine-needle biopsy and an evaluation of their
combined use in the diagnosis of breast lesions: report on a prospective study in 1244 women with symptoms. Ann Surg. 1975 Jul;182(1):
1-8.
4. Chaney AW, Pollack A, McNeese MD, Zagars GK, Pisters PW, Pollock RE, et al. Primary treatment of cystosarcoma phyllodes of the
breast. Cancer. 2000 Oct 1;89(7):1502-11.
5. Foster MC, Helvie MA, Gregory NE, Rebner M, Nees AV, Paramagul C. Lobular carcinoma in situ or atypical lobular hyperplasia at
core-needle biopsy: is excisional biopsy necessary? Radiology. 2004 Jun;231(3):813-9.
6. Maganini RO, Klem DA, Huston BJ, Bruner ES, Jacobs HK. Upgrade rate of core biopsy-determined atypical ductal hyperplasia by open
excisional biopsy. Am J Surg. 2001 Oct;182(4):355-8.
7. Yeh IT, Dimitrov D, Otto P, Miller AR, Kahlenberg MS, Cruz A. Pathologic review of atypical hyperplasia identified by image-guided
breast needle core biopsy. Correlation with excision specimen. Arch Pathol Lab Med. 2003 Jan;127(1):49-54.
v v v
¡ÒõÃǨ¤Ñ´¡ÃͧáÅÐÇÔ¹¨Ô ©ÑÂÁÐàÃç§àµÒ¹Á
34
¡ÒõÃǨ¤Ñ´¡Ãͧ ¡ÒõÃǨ¤Ñ´¡Ãͧ¢Ñé¹µ¹
ËÃ×ÍáÊ´§ÍÒ¡ÒÃ
Consider endocrine
Bilateral Pregnancy Pregnancy Negative evaluation
Milky concern test
Positive Refer to obstetrician
BI-RADS
Final Mammography Ductography
Persistent áÅÐ/ËÃ×ÍU/S (optional) Duct excision
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
· Breast Assessment
Spontaneous, Imaging* Category 1-3**
19/2/2551, 20:58
unilateral · Guaiac or
single duct, cytology BI-RADS Benign/
or serous { optional
} Final Tissue indeterminate
sanguinous Assessment Diagnosis
Category 4-5** Malignant Cancer treatment
* ÍÒ¨·Ó Ductography ÃÇÁ´ÇÂ
** ´Ùá¹Ç·Ò§¡ÒöÒÂÀÒ¾ÃѧÊÕàµÒ¹Á (mammography)
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á 35
v v v
36
ÁÕʧÔè ¼Ô´»¡µÔÃÇ Á ´ÙµÒÁá¹Ç·Ò§ÇÔ¹Ô¨©ÑÂáÅÐÃÑ¡ÉҢͧàÃ×èͧ¹Ñé¹æ
Mastalgia
Abnormal ´ÙµÒÁá¹Ç·Ò§¡ÒôÙáÅ
àÃ×èͧ Abnormal Imaging
·ÓImaging µÒÁ¢Íº§ªÕé
Normal Reassure ± Medication
äÁÁÕÊÔ觼Դ»¡µÔ ¾Ô¨ÒÃ³Ò Imaging*
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
19/2/2551, 20:58
* ·Ó Imaging µÒÁ¢Íº§ªÕé
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á 37
Mastalgia
ÍÒ¡ÒÃà¨çººÃÔàdzàµÒ¹Á໹ÍÒ¡ÒÃ·Õ¾è ººÍÂã¹¼ËÙ Ô§áÅÐÁÕ¤ÇÒÁÃعáç·Õáè µ¡µÒ§¡Ñ¹ä» ầÍÍ¡
໹ÍÒ¡ÒÃà¨çº·Õàè µÒ¹Á áÅÐà¨çººÃÔàdz chest wall* «Ö§è ÍÒ¨¨ÐÃعáçÁÒ¡¨¹ÁռŵͤسÀÒ¾ªÕÇµÔ ä´ áÅÐÍÒ¨¨Ð
໹àÃ×Íé ÃÑ§ä´ºÍ Â æ
ÍÒ¡ÒÃà¨çºàµÒ¹ÁÍÒ¨µÃǨ¾ºÊÔ§è ¼Ô´»¡µÔ͹×è æ ÃÇÁ´ÇÂä´ àª¹ ¡Í¹ ¼»Ù Ç Â·ÕÁè ÍÕ Ò¡ÒÃà¨çºàµÒ¹Áà¾Õ§
ÍÂÒ§à´ÕÂÇáÅÐäÁÁ¤Õ ÇÒÁ¼Ô´»¡µÔ͹×è ÊǹãËäÁä´ÁÊÕ Òà˵بҡÁÐàÃç§
á¹Ç·Ò§¡ÒôÙáÅÍÒ¡ÒÃà¨çºàµÒ¹Á¹Ñ¹é µÍ§µÃǨ»ÃÐàÁÔ¹ÇÒÁÕʧÔè ¼Ô´»¡µÔ͹×è ÃÇÁ´ÇÂËÃ×ÍäÁ «Ö§è µÍ§
´ÙáÅ仵ÒÁÊÔ§è ¼Ô´»¡µÔ¹¹Ñé હ àÃ×Íè §¡Í¹, nipple discharge áµ¶Ò äÁÁÊÕ §Ôè ¼Ô´»¡µÔ͹×è ÃÇÁ´Ç ã˾¨Ô ÒÃ³Ò·Ó breast
imaging µÒÁ¢Íº§ªÕé (´Ùá¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡ÃͧÁÐàÃç§àµÒ¹Á)
㹡óշÕè·Ó imaging ¶Ò¾ºÊÔ觼Դ»¡µÔ ãË´ÙáŵÒÁá¹Ç·Ò§¡ÒÃÇÔ¹Ô¨©Ñ¹Ñé¹ áµ¶ÒäÁ¾ºÊÔ觼Դ»¡µÔ
¡çãˤÓá¹Ð¹Ó¼»Ù Ç ÂáÅСÒÃÃÑ¡ÉÒµÒÁ¤ÇÒÁ¨Ó໹
㹡óշÕèäÁä´·Ó imaging áÅÐäÁ¾ºÊÔ觼Դ»¡µÔã´æ ãˤÓá¹Ð¹Óà¡ÕèÂǡѺÍÒ¡ÒÃà¨çºàµÒ¹ÁáÅÐ
¾Ô¨ÒóÒãË¡ÒÃÃÑ¡ÉÒµÒÁ¤ÇÒÁ¨Ó໹
v v v
* Chest wall pain ËÁÒ¶֧ No pattern; any age; almost always unilateral; consider costochondritis (Tietze's syndrome), musculo-skeletal
origin, surgical trauma, referred pain.
á¹Ç·Ò§¡ÒÃÃÑ¡ÉÒÁÐàÃç§àµÒ¹Áâ´Â¡ÒüҵѴ
á¹Ç·Ò§¡ÒÃÃÑ¡ÉÒÁÐàÃç§àµÒ¹Áâ´Â¡ÒüҵѴ ầ¡ÒÃÃÑ¡ÉÒµÒÁÃÐÂТͧâä (staging) ä´´§Ñ ¹Õé
Stage 0 (Pure Noninvasive Carcinomas)
1. Lobular Carcinoma In Situ (LCIS)
á¹Ð¹Ó¡ÒÃÃÑ¡ÉÒ LCIS ´Ç¡ÒÃà½ÒÃÐÇѧ (surveillance)(1)
à¹×èͧ¨Ò¡ LCIS ÁÕâÍ¡ÒÊà¡Ô´ invasive carcinoma µèÓ (»ÃÐÁÒ³ 21% over 15 years) ÍÂÒ§äÃ
¡çµÒÁ¼»Ù Ç Â¡ÅÁØ ¹Õµé Í §¹Ñ´ÁÒµÔ´µÒÁ¡ÒÃÃÑ¡ÉÒâ´Â¡ÒõÃǨÃÒ§¡Ò·ء 6-12 à´×͹ áÅÐ ·Ó mammogram »ÅФÃѧé
¹Í¡¨Ò¡¹ÕÍé Ò¨¾Ô¨ÒÃ³Ò risk reduction «Ö§è ã¹»¨¨Øº¹Ñ ÁÕ¢Í á¹Ð¹Ó 2 ÇÔ¸Õ
1. â´Â¡ÒÃãªÂÒ à¾×Íè Å´âÍ¡ÒÊà¡Ô´ invasive carcinoma «Ö§è á¹Ð¹ÓãËÂҴѧ¹Õé
- tamoxifen(2) ໹àÇÅÒ 5 »
- ÊǹÂÒµÑÇÍ×¹è હ ¡ÅÁØ aromatase inhibitors ã¹¢³Ð¹ÕÂé §Ñ ÁÕ¢Í ÁÙÅäÁà¾Õ§¾Í(1, 3)
2. â´Â¡ÒüҵѴ ¡ÒÃ·Ó bilateral prophylactic mastectomies ± reconstruction ¨Ðãªà»¹
ºÒ§¡Ã³Õà·Ò¹Ñé¹ àª¹ã¹¼Ù»Ç high risk, äÁÂÍÁÃѺÍѵÃÒàÊÕ觷Õèà¾ÔèÁ¢Ö鹢ͧ¡ÒÃ໹ÁÐàÃç§àµÒ¹Á·Ñé§Êͧ¢Ò§
ã¹Í¹Ò¤µ áÅФÇõѴàµÒ¹ÁÍÍ¡·Ñ§é 2 ¢Ò§ à¾ÃÒÐÇÒâÍ¡ÒÊà¡Ô´ invasive carcinoma ã¹¼»Ù Ç Â LCIS ¨Ðà·Ò¡Ñ¹·Ñ§é
2 ¢Ò§ (8-11 à·Ò¢Í§»ÃЪҡ÷ÑÇè ä» ËÃ×Í»ÃÐÁÒ³ 1% µÍ», subsequent carcinoma ໹ invasive ductal ÁÒ¡¡ÇÒ
lobular carcinoma)(4)
͹Ö觡ÒÃ·Ó mastectomy ± contralateral breast biopsy ã¹»¨¨ØºÑ¹äÁ¹ÔÂÁáÅÇ à¹×èͧ¨Ò¡¼Ù»ÇÂ
ÊǹãË·àÕè »¹ LCIS ÁÕâÍ¡ÒÊà¡Ô´ invasive carcinoma µèÓ ¡ÒÃ·Ó mastectomy ÁÕ¢Í àÊÕÂÁÒ¡¡ÇÒáÅÐà»Å×ͧ¤Òãª¨Ò Â
Êǹ¡ÒõѴªÔ¹é à¹×Íé ¨Ò¡àµÒ¹ÁÍÕ¡¢Ò§¡çÍÒ¨¨ÐäÁä´µÓá˹§·Õàè »¹ÁÐàÃç§ âÍ¡Òʢͧ¡ÒÃà¡Ô´ÁÐàÃç§Âѧ¤§à·Òà´ÔÁ(5)
2. Ductal Carcinoma In Situ (DCIS)
¡ÒÃÃÑ¡ÉÒÁÕ·Ò§àÅ×Í¡´Ñ§¹Õé
1. Total mastectomy ± reconstruction
2. Wide local excision + radiotherapy
3. Wide local excision alone
¡ÒÃÃÑ¡ÉÒâ´Â total mastectomy ໹·ÕèÂÍÁÃѺÇÒä´¼Å´Õ (survival 98-99%) ÁÕâÍ¡ÒÊà¡Ô´ local
recurrence (0-2%) ä´¹Í Â¡ÇÒÇÔ¸ÍÕ ¹×è æ ´Ñ§¹Ñ¹é DCIS ·Ø¡¢¹Ò´ËÃ×ÍËÅÒµÓá˹§ÊÒÁÒöàÅ×Í¡ãªÇ¸Ô ¹Õ Õé
¡ÒÃÃÑ¡ÉÒâ´Â wide local excision + radiotherapy ÁÕâÍ¡ÒÊà¡Ô´ local recurrence ¹Í¡ÇÒ¡Ò÷Ó
wide local excision à¾Õ§ÍÂÒ§à´ÕÂÇ ¤×Í ¨Ò¡ 10.4% ໹ 7.5% ·Õè 5 »(6, 7) ¨Ö§à»¹·ÕÂè ÍÁÃÑºä´ áÅÐ overall survival
¡çà·Ò¡Ñº¡ÒÃÃÑ¡ÉÒâ´Â total mastectomy ¡Ò÷ӼҵѴ¤ÇÃä´ free margin áÅеÒÁ´Ç¡ÒéÒÂáʧ(7) «Öè§
ÇÔ¸¹Õ äÕé ÁàËÁÒжÒÁÕ DCIS ËÅÒµÓá˹§ ËÃ×͡͹âµÁÒ¡áÅм»Ù Ç ÂµÍ§äÁÁ¢Õ Í ËÒÁ㹡ÒéÒÂáʧ
¡ÒÃÃÑ¡ÉÒâ´Â wide local excision alone ãªã¹¤¹ä¢·ÁÕè ¡Õ Í ¹àÅç¡¡ÇÒ 0.5 ૹµÔàÁµÃ, low grade,
noncomedonecrosis ¹Í¡¨Ò¡¹ÕÂé §Ñ µÍ§¤Ó¹Ö§¶Ö§ ÍÒÂآͧ¼»Ù Ç Â áÅÐ margin ¢Í§¡ÒüҵѴ´ÇÂ(8)
2. ¡ÒÃ·Ó sentinel lymph node biopsy (SLNB) à» ¹ ÍÕ ¡ ·Ò§àÅ× Í ¡á·¹ ALND ã¹¡Ã³Õ ·Õè
¤Ò´ÇÒäÁÁ¡Õ ÒáÃШÒ¢ͧÁÐàÃç§ä»ÂѧµÍÁ¹éÓàËÅ×ͧ·ÕÃè ¡Ñ áÃ
Breast reconstruction
¡ÒÃ·Ó Breast reconstruction ÊÒÁÒö·Óä´·§Ñé Immediate ËÃ×Í Delayed reconstruction 㹡ÒÃ·Ó Im-
mediate breast reconstruction ¡ÒÃ·Ó Skin sparing mastectomy ¾ºÇÒ¼Å㹡ÒèѴ¡Òà Primary tumor
ã˼Åà·Õºà·Ò¡ÒÃ·Ó Standard mastectomy á¹Ð¹ÓÇÒäÁ¤ÇÃ·Ó immediate breast reconstruction ã¹¼»Ù Ç ÂµÍ仹Õé
- Non-resectable local chest wall disease
- Rapidly progressive systemic disease
- Patients who have serious co-morbidity
- Patients who are psychologically unsuitable
References
1. Fisher B, Costantino JP, Wickerham DL, Cecchini RS, Cronin WM, Robidoux A, et al. Tamoxifen for the prevention of breast cancer:
current status of the National Surgical Adjuvant Breast and Bowel Project P-1 study. J Natl Cancer Inst. 2005 Nov 16;97(22):1652-62.
2. Gail MH, Costantino JP, Bryant J, Croyle R, Freedman L, Helzlsouer K, et al. Weighing the risks and benefits of tamoxifen treatment
for preventing breast cancer. J Natl Cancer Inst. 1999 Nov 3;91(21):1829-46.
3. Vogel VG, Costantino JP, Wickerham DL, Cronin WM, Cecchini RS, Atkins JN, et al. Effects of tamoxifen vs raloxifene on the risk of
developing invasive breast cancer and other disease outcomes: the NSABP Study of Tamoxifen and Raloxifene (STAR) P-2 trial. Jama.
2006 Jun 21;295(23):2727-41.
4. Chuba PJ, Hamre MR, Yap J, Severson RK, Lucas D, Shamsa F, et al. Bilateral risk for subsequent breast cancer after lobular
carcinoma-in-situ: analysis of surveillance, epidemiology, and end results data. J Clin Oncol. 2005 Aug 20;23(24):5534-41.
5. Cody HS, 3rd. Routine contralateral breast biopsy: helpful or irrelevant? Experience in 871 patients, 1979-1993. Ann Surg. 1997
Apr;225(4):370-6.
6. Fisher B, Dignam J, Wolmark N, Mamounas E, Costantino J, Poller W, et al. Lumpectomy and radiation therapy for the treatment of
intraductal breast cancer: findings from National Surgical Adjuvant Breast and Bowel Project B-17. J Clin Oncol. 1998 Feb;16(2):
441-52.
7. Julien JP, Bijker N, Fentiman IS, Peterse JL, Delledonne V, Rouanet P, et al. Radiotherapy in breast-conserving treatment for ductal
carcinoma in situ: first results of the EORTC randomised phase III trial 10853. EORTC Breast Cancer Cooperative Group and EORTC
Radiotherapy Group. Lancet. 2000 Feb 12;355(9203):528-33.
8. Silverstein MJ, Lagios MD, Groshen S, Waisman JR, Lewinsky BS, Martino S, et al. The influence of margin width on local control of
ductal carcinoma in situ of the breast. N Engl J Med. 1999 May 13;340(19):1455-61.
9. Kelly TA, Kim JA, Patrick R, Grundfest S, Crowe JP. Axillary lymph node metastases in patients with a final diagnosis of ductal
carcinoma in situ. Am J Surg. 2003 Oct;186(4):368-70.
10. Goyal A, Douglas-Jones A, Monypenny I, Sweetland H, Stevens G, Mansel RE. Is there a role of sentinel lymph node biopsy in ductal
carcinoma in situ?: analysis of 587 cases. Breast Cancer Res Treat. 2006 Aug;98(3):311-4.
11. Veronesi P, Intra M, Vento AR, Naninato P, Caldarella P, Paganelli G, et al. Sentinel lymph node biopsy for localised ductal carcinoma
in situ? Breast. 2005 Dec;14(6):520-2.
12. Zavagno G, Carcoforo P, Marconato R, Franchini Z, Scalco G, Burelli P, et al. Role of axillary sentinel lymph node biopsy in patients
with pure ductal carcinoma in situ of the breast. BMC Cancer. 2005 Mar 11;5:28.
13. Fisher B, Dignam J, Wolmark N, Wickerham DL, Fisher ER, Mamounas E, et al. Tamoxifen in treatment of intraductal breast cancer:
National Surgical Adjuvant Breast and Bowel Project B-24 randomised controlled trial. Lancet. 1999 Jun 12;353(9169):1993-2000.
14. Fisher B, Land S, Mamounas E, Dignam J, Fisher ER, Wolmark N. Prevention of invasive breast cancer in women with ductal carcinoma
in situ: an update of the national surgical adjuvant breast and bowel project experience. Semin Oncol. 2001 Aug;28(4):400-18.
15. Fisher B et al: Twenty-year follow-up of a randomized trial comparing total mastectomy, lumpectomy, and lumpectomy plus irradiation
for the treatment of invasive breast cancer, N Engl J Med 2002; 347:1233.
v v v
á¹Ç·Ò§ÃѧÊÕÃÑ¡ÉÒã¹¼Ù»ÇÂÁÐàÃç§àµÒ¹Á
(Radiation Therapy for Breast Cancer)
1. Postmastectomy Radiotherapy
໹·ÕÂè ÍÁÃѺ¡Ñ¹áÅÇÇÒ¡ÒüҵѴ modified radical mastectomy ໹¡ÒÃÃÑ¡ÉÒËÅÑ¡·Õ¶è Í× à»¹¡ÒÃÃÑ¡ÉÒ
ẺÁҵðҹÊÓËÃѺ¼Ù»ÇÂÁÐàÃç§àµÒ¹Á·Õè໹ operable breast cancer(1) ÍÂÒ§äáçµÒÁÁռٻǨӹǹ˹Öè§
Âѧ¤§ÁÕ¡ÒáÅѺ໹«éӢͧâäà¡Ô´¢Ö¹é ·Õºè ÃÔàdzá¼Å¼ÒµÑ´º¹Ë¹ÒÍ¡áÅеÍÁ¹éÓàËÅ×ͧ¢Ò§à¤Õ§(2)
¨Ò¡¡ÒÃÈÖ¡ÉÒÃÒ§ҹÍغµÑ ¡Ô Òó¡ÒáÅѺ໹«éӢͧâä੾ÒзÕè (locoregional recurrence) ËÅѧ¨Ò¡
¡ÒÃ·Ó modified radical mastectomy ¾ºÇÒ¢Ö¹é ¡Ñº T áÅÐ N stage(2-5)
Êǹã˨Ðà¡Ô´¡ÒáÅѺ໹«éÓ·ÕèºÃÔàdz chest wall áÅÐ supraclavicular nodes ÊǹµÓá˹§Í×è¹æ
¾ºä´¹Í  ¹Í¡¨Ò¡¹ÕÊé §Ôè ÊӤѤ×Í àÁ×Íè ÁÕ¡ÒáÅѺ໹«éӢͧâä੾ÒзÕáè ÅÇ ¨Ð¡ÍãËà¡Ô´ÍÒ¡ÒÃÍѹäÁ¾§Ö »ÃÐʧ¤
ËÃ×ͤÇÒÁ·Ø¡¢·ÃÁÒ¹µÍ¼Ù»Ç હ ÁÕ ulceration, bleeding, pain, arm edema ËÃ×ÍÍÒ¨ÁÕ brachial plexus
compression áÅÐÁÑ¡¨ÐäÁÊÒÁÒö¤Çº¤ØÁâää´
ÃÒ§ҹ¡ÒÃÈÖ¡ÉÒ¡ÒÃãªÃѧÊÕÃÑ¡ÉÒËÅѧ¡Ò÷ӼҵѴ mastectomy ¾ºÇÒÊÒÁÒöŴÍغѵԡÒó¡ÅѺ
໹«éӢͧâä੾ÒзÕèŧä´ÍÂÒ§ÁÕ¹ÑÂÊÓ¤Ñ·Ò§Ê¶ÔµÔ â´Â¨ÐÅ´ÍغѵԡÒó¡ÅѺ໹«éӢͧâää´ÍÂÒ§¹ÍÂ
¤ÃÖ§è Ë¹Ö§è ¶Ö§Êͧã¹ÊÒÁ¢Í§¼»Ù Ç Â·Õàè »¹¡ÅÁØ high risk(6-9)
»¨¨Øº¹
Ñ ¢Íº§ªÕ¢é ͧ¡ÒÃãË postmastectomy radiotherapy ÁÕ´§Ñ ¹Õ¤é Í×
1. Four or more positive axillary lymph nodes
2. ³ T3 tumor
3. Positive or close (< 1-2 mm) surgical margins (µÒÁ´ØžԹ¨Ô ¢Í§á¾·Â¼ÃÙ ¡Ñ ÉÒ)
4. Pectoral fascia involvement
5. Grossly extracapsular invasion (fixed or matted nodes)
ËÁÒÂà˵Ø: ÊÒÁÒöãË postmastectomy radiotherapy µÒÁ´ØžԹ¨Ô ¢Í§á¾·Â¼ÃÙ ¡Ñ ÉÒ㹡óÕ
1. 1-3 positive axillary nodes â´Â´ÙµÒÁ»¨¨ÑÂàÊÕÂè § ä´á¡ inadequate axillary lymph node
dissection, T size, grade, margin, ÍÒÂØ ÏÅÏ
2. T2 tumor àÁ×Íè à·Õº¡Ñº¢¹Ò´àµÒ¹Á¢Í§¼»Ù Ç ÂáÅÇÁÕ¢¹Ò´ãË ËÃ×ÍÁÕÀÒÇÐ extensive
lymphovascular invasion
á¹Ð¹ÓãËàÃÔèÁÃѧÊÕÃÑ¡ÉÒ ÀÒÂã¹ 4-8 ÊÑ»´ÒË ËÅѧ¼ÒµÑ´ áµËÒ¡ÁÕ¤ÇÒÁ¨Ó໹µÍ§ãËà¤ÁպӺѴ´ÇÂ
ÊÒÁÒöàÃÔÁè ÃѧÊÕÃ¡Ñ ÉÒËÅѧãËÂÒà¤ÁպӺѴ¤ÃºáÅÇ áµäÁ¤ÇÃà¡Ô¹ 6 à´×͹ËÅѧ¼ÒµÑ´
* Internal mammary node radiation for clinical or pathological internal mammary node positive, otherwise the treatment to the internal
mammary field is at the discretion of radiation oncologist. (Category 2B)
* Internal mammary node radiation for clinical or pathological internal mammary node positive, otherwise the treatment to the internal
mammary field is at the discretion of radiation oncologist. (Category 2B)
ËÁÒÂà˵Ø: á¹Ð¹ÓãË Boost tumor bed 㹼ٻǷÕèÁÕ»¨¨ÑÂàÊÕ觵͡ÒÃà¡Ô´ Local failure ´Ñ§¹Õé ÍÒÂØ
¹Í¡ÇÒ 50 » positive axillary nodes, lymphovascular invasion, close margins
* Radiation to the whole breast reduces recurrence rates about 50%. Factors determine risk of local recurrence include tumor size, grade,
margin, and age.
¹ÔÂÁ㪠palliative whole brain radiation â´Â㪻ÃÔÁÒ³ÃѧÊÕ 30 Gy / 10F / 2 wks. áÅÐÍÒ¨¾Ô¨ÒÃ³Ò local tumor
boost ´Ç stereotactic radiotherapy (SRT) ËÃ×Í stereotactic radiosurgery (SRS) 㹡óշÕèÁÕ brain metastasis
äÁà¡Ô¹ 3 lesions(26-29)
3. ¡ÒÃá¾Ã¡ÃШÒ¢ͧÁÐàÃç§àµÒ¹ÁÊÙµÍÁ¹éÓàËÅ×ͧ㹪ͧ·Ãǧ͡ ÍÒ¨¡ÍãËà¡Ô´ÍÒ¡Òà superior
vena cava obstruction (SVCO) ÃѧÊÕÃÑ¡ÉÒ¡ç໹¡ÒÃÃÑ¡ÉÒÇÔ¸Õ˹Ö觷ÕèÁÕ»ÃÐÊÔ·¸ÔÀÒ¾áÅÐä´¼ÅàÃçÇ ÊǹãËãª
»ÃÔÁÒ³ÃѧÊÕ 30 Gy / 10F / 2 wks.
5. Locoregional Recurrence
¼Ù»ÇÂÁÐàÃç§àµÒ¹Á·ÕèÁÕâä¡ÅѺ໹«éÓ੾ÒзÕèà¾Õ§ÍÂÒ§à´ÕÂÇ áº§Í͡໹ 2 ¡ÅØÁ¤×Í ¡ÅØÁ·Õèä´ÃѺ
¡ÒÃÃÑ¡ÉÒẺ mastectomy ¡Ñº¡ÅÁØ ·Õäè ´ÃºÑ ¡ÒÃÃÑ¡ÉÒẺ BCT Áҡ͹
¼»Ù Ç Â·ÕÃè ºÑ ¡ÒÃÃÑ¡ÉÒẺ mastectomy
- ¶Ò·Ó¼ÒµÑ´ä´ ¤ÇþԨÒóҼҵѴ¡Í¹ÁÐàÃç§ÍÍ¡áÅǵÒÁ´Ç¡ÒéÒÂÃѧÊÕ ¶ÒäÁà¤Â©ÒÂÃѧÊÕ
Áҡ͹
- 㹡óշÕèà¤Â©ÒÂÃѧÊÕÁҡ͹ ËÒ¡¾Ô¨ÒóÒáÅÇÇÒ¡ÒéÒÂÃѧÊÕ«éÓ¹Ñé¹»ÅÍ´ÀÑÂáÅÐà¡Ô´
»ÃÐ⪹µÍ ¼»Ù Ç ÂÊÒÁÒö©ÒÂÃѧÊÕ«éÓä´
- ¶Ò·Ó¼ÒµÑ´äÁä´ãËãªÃ§Ñ ÊÕÃ¡Ñ ÉÒ(30-31)
- ÊÓËÃѺ Systemic treatmentã˾¨Ô ÒóÒ໹ÃÒÂæ ä»(32-34)
¼»Ù Ç Â·ÕÃè ºÑ ¡ÒÃÃÑ¡ÉÒẺ BCT
- ¤Ç÷ӡÒüҵѴµÒÁ´ØžԹԨ¢Í§ÈÑÅÂá¾·Â Êǹ¡ÒéÒÂÃѧÊÕáÅÐ Systemic treatment ãË
¾Ô¨ÒóÒ໹ÃÒÂæ ä»(32-34)
6. Ovarian Castration
ÊÒÁÒöãªã¹¼Ù»Ç Premenopause ·ÕèÁÕ¡ÒÃá¾Ã¡ÃШÒ¢ͧâäáÅÐ Hormone Receptor Positive
â´Â©ÒÂÃѧÊÕ¤Ãͺ¤ÅØÁ true pelvis dose 14 - 20 Gy ã¹ 4-5 ¤ÃÑ§é ¢Ö¹é Í¡٠ºÑ ÊÀÒ¾ áÅÐÀÒÇлÃШÓà´×͹¢Í§ ¼»Ù Ç Â(35)
à·¤¹Ô¤¡ÒéÒÂÃѧÊÕ(36, 37)
1. ¡ÒéÒÂÃѧÊÕºÃÔàdz chest wall ËÃ×Í intact breast (ÃÙ»·Õè 1)
â´Â㪠medial áÅÐ lateral tangential portals ¤Ãͺ¤ÅØÁ chest wall ËÃ×Í whole breast áÅоÂÒÂÒÁãË
ÃѧÊÕ¶¡Ù à¹×Íé »Í´áÅÐËÑÇã¨ãË¹Í Â·ÕÊè ´Ø Áբͺࢵ¢Í§ field ´Ñ§¹Õé
- Upper margin : ¢ÍºÅÒ§¢Í§ clavicular head
- Medial margin : midline ËÃ×Í¢ÒÁ midline ä»´Ò¹µÃ§¢ÒÁ»ÃÐÁÒ³ 1 ૹµÔàÁµÃ
- Lateral margin : mid axillary line ËÃ×Í»ÃÐÁÒ³ 2 ૹµÔàÁµÃ ¨Ò¡¢Íº¢Ò§¢Í§ breast tissue
A. B.
ÊÓËÃѺ axillary recurrence ¾ºä´»ÃÐÁÒ³ 0.5-3% à·Ò¹Ñ¹é ËÅѧ¨Ò¡¡ÒÃ·Ó axillary dissection of level
I áÅÐ II ËÃ×;º axillary recurrence à¾Õ§ 1% 㹼ٻǷÕèÁÕ axillary positive 1-3 nodes ·Õè¼ÒµÑ´µÍÁ
¹éÓàËÅ×ͧ·ÕÃè ¡Ñ áÃÍÍ¡ÁÒ 10 nodes áÅоºÇÒÁÕ axillary recurrence ä´ 6% ã¹¼»Ù Ç Â·ÕÁè Õ axillary positive 1-3 nodes
·Õè¼ÒµÑ´µÍÁ¹éÓàËÅ×ͧ·ÕèÃÑ¡áÃÍÍ¡ÁÒ 4 nodes(39-42) ´Ñ§¹Ñ鹨֧äÁÁÕ¤ÇÒÁ¨Ó໹µÍ§©ÒÂÃѧÊÕºÃÔàdzÃÑ¡áà ¡àǹ
áµäÁÊÒÁÒö¼ÒµÑ´µÍÁ¹éÓàËÅ×ͧÍÍ¡ä´ËÁ´ ,㹡óշÁÕè Õ clinical matted axillary nodes , extracapsular invasion
ÍÒ¨¾Ô¨ÒóҩÒÂÃѧÊÕ·Õè axilla ´ÇÂ
¾Ô¨ÒóÒ㪡ÒéÒÂÃѧÊÕÊÒÁÁÔµÔ ¶Ò¡ÒéÒÂÃѧÊÕÊͧÁÔµÔ·Óã˻ʹáÅÐËÑÇã¨ä´ÃѺ»ÃÔÁÒ³ÃѧÊÕÊÙ§
·Ñ§é ¹Õ¢é ¹Öé Í¡٠ºÑ ´ØžԹ¨Ô ¢Í§á¾·Â¼ÃÙ ¡Ñ ÉÒ(43)
References
1. Halsted WS. The results of operations for the cure of cancer of the breast performed at the johns Hopkins Hospital from June 1889 to
January, 1984. Johns Hopkins Hosp Bull 1894-1895; 4: 297.
2. Haagensen CD. Result with Halsted's radical mastectomy. In: Haagensen CD, ed. Disease of the Breast, 3rd edition. Philadelphia: WB
Saunder Company, 1986: 903-932.
3. Stefanik D, Goldberg R, Byrne P, et al. Local-regional failure in patients treated with adjuvant chemotherapy for breast cancer. J Clin
Oncol 1985; 3: 660-665.
4. Arriagada R, Le MG. Adjuvant radiotherapy in breast cancer-the treatment of lymph node areas. Acta Oncol 2000; 39: 295-305.
5. Fowble B, Gray R, Gilchrist K, et al. Identification of a subgroup of patients with breast cancer and histologically positive axillary nodes
receiving adjuvant chemotherapy who may benefit from postoperative radiotherapy. J Clin Oncol 1988; 6: 1107-1117.
6. Fisher B, Redmond C, Fisher ER, et al. Ten-year results of a randomized clinical trial comparing radical mastectomy and total
mastectomy with or without radiation. N Engl J Med 1985; 312: 674-681.
7. Wallgren A, Arner O, Bergstrom J, et al. Radiation therapy in operable breast cancer: Results from the Stockholm trial on adjuvant
radiotherapy. Int J Radiat Oncol Biol Phys 1986; 12: 533-537.
8. Rutqvist LE, Cedermark B, Glas U, et al. Radiotherapy, chemotherapy, and tamoxifen as adjuncts to surgery in early breast cancer: A
summary of three randomized trials. Int J Radiat Oncol Biol Phys 1989; 16: 629-639.
9. Overgaard M, Christensen JJ, Johansen H, et al. Evaluation of radiotherapy in high-risk breast cancer patients: Report from the Danish
Breast Cancer Cooperative Group (DBCG 82) Trial. Int J Radiat Oncol Biol Phys 1990; 19: 1121-1124.
10. Fisher B. Anderson S, Redmond CD, et al. Re-analysis and result after 12 years of follow up in a randomized clinical trial comparing
total mastectomy with lumpectomy with or without irradiation in the treatment of breast cancer. N Engl J Med 1995; 333: 1456-1461.
11. Clark RM, Whelan T, Levine M, et al. Randomized clinical trial of breast irradiation following lumpectomy and axillary dissection for
node negative breast cancer: An update. J Natl Cancer Inst 1998; 88: 1659-1664.
12. Van Dongen JA, Bartelink H, Fentiman IS, et al. Randomized clinical trial to assess the value of breast conserving therapy in stage I and
II breast cancer: EORTC 10801 trial. J Natl Cancer Inst Monogr 1992; 11: 15-18.
13. Van Dongen JA, Voogd AC, Fentiman IS, et al. Long term results of a randomized trial comparing breast conserving therapy with
mastectomy: EORTC 10801 trial. J Natl Cancer Inst 2000; 92: 1143-1150.
14. Bilchert-TM, Rose C, Andersen JA, et al. Danish randomized trial comparting breast conservation therapy with mastectomy: six years
of life-table analysis. J Natl Cancer Inst Monogr 1992; 11: 19-25.
15. Sarragin D, Le MG, Arriagada R, et al. Ten-year results of a randomized trial comparing a conservative treatment to mastectomy in early
breast cancer. Radiother Oncol 1989; 14: 177-184.
16. Morris AD, Morris RD, Wilson JF, et al. Breast conserving therapy VS mastectomy in early breast cancer: a meta-analysis of 10-year
survival. Cancer J Sci Am 1997; 3: 6-12.
17. Fisher B, Constantino J, Redmond C, et al. Initial results from a randomized trial evaluating lumpectomy and radiation therapy for the
treatment of intraductal breast cancer. N Engl J Med 1993; 328: 1581-1586.
18. Fisher B, Dignam J, Wolmark N, et al. Lumpectomy and radiation therapy for the treatment of intraductal breast cancer: finding from
NSABP B-17. J Clin Oncol 1998; 16: 441-452.
19. Julien J-P, Bijker N, Fentiman IS, et al. Radiotherapy in breast conserving treatment for ductal carcinoma in situ: first results of the
EORTC randomized phase III Trial 10853. Lancet 2000; 355: 528-533.
20. Perez CA, Graham ML, Taylor ME, et al. Management of Locally advanced Carcinoma of the Breast: I. Non-Inflammatory. Cancer
1994; 74: 453-465.
21. Sheldon T, Hayes DF, Cady B, Parker L, et al. Primary radiation therapy for locally advanced breast cancer. Cancer 1984; 60: 1219-1225.
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33-38.
25. Ratanatharathorn V, Powers WE, Moss WT, Perez CA. Bone metastasis: review and critical analysis of random allocation trials of local
field treatment. Int J Radiat Oncol Biol Phys 1999; 44: 1-18.
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Radiation Oncology, 3rd edition. Philadelphia: Lippincott-Raven Publishers, 1998.
28. Shirato H, Takamura A, Tomita M, et al. Stereotactic irradiation without whole-brain irradiation for single brain metastasis. Int J Radiat
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29. Adler JR, Cox RS, Kaplan I, et al. Stereotactic radiosurgical treatment of brain metastases. J Neurosurg 1992; 76: 444-449.
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management. Int J Radiat Oncol Biol Phys 1990; 19: 851-858.
31. Kenda R, Lozza L, Zucali R. Results of irradiation in the treatment of chest wall recurrent breast cancer. Radiother Oncol 1992; 24
(suppl 1): S41a (abst)
32. Fowble B, Solin LJ, Schultz DJ, Rubenstein J, Goodman RL. Breast recurrence following conservative surgery and radiation: patterns
of failure, prognosis, and pathologic findings from mastectomy specimens with implication of treatment. Int J Radiat Oncol Biol Phys
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33. Dalberg K, Mattsson A, Sandelin K, Rutqvist LE. Outcome of treatment for ipsilateral breast tumor recurrence in early breast cancer.
Breast cancer Res Treat 1998; 49: 69-78.
34. Stotter A, Kroll S, McNeese M, Holmes F, Oswald MJ, Romsdahl M. Salvage treatment of locoregional recurrence following breast
conservation therapy for early breast cancer. Eur J Surg Oncol 1991; 17: 231-236.
35. Radiation Treatment of Benign disease. In: Chao KSC, Perez CA, Brady LW, eds Radiation Oncology Management Decisions 2nd
editian. Philadephia: Lippvicott-Williams+Wilkins 2002: 677-688.
36. Bornstein BA, Cheng CW, Rhodes LM, et al. Can simulation measurement be used to predict the irradiated lung volume in the tangential
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v v v
á¹Ç·Ò§¡ÒÃÃÑ¡ÉÒàÊÃÔÁËÅѧ¼ÒµÑ´ã¹¼Ù»ÇÂÁÐàÃç§àµÒ¹ÁÃÐÂÐáá
(Guideline for Adjuvant Systemic Therapy in Early Breast Cancer)
¤ÓÊÓ¤Ñ
1. ÁÐàÃç§àµÒ¹ÁÃÐÂÐáá (early stage breast cancer) ¼Ù»Ç·ÕèÁÕÃÍÂâäÍÂÙ੾ÒзÕèàµÒ¹ÁáÅÐ/
ËÃ×͵ÍÁ¹éÓàËÅ×ͧ·ÕÃè ¡Ñ áà ÂѧäÁÁ¡Õ ÒÃá¾Ã¡ÃШÒÂÅØ¡ÅÒÁÁÒÂѧ¼ÔÇ˹ѧ ËÃ×͵ÍÁ¹éÓàËÅ×ͧ·Õºè ÃÔàdzÍ×¹è ËÃ×Í·Õè
ÍÇÑÂÇзÕËè Ò §ä¡ÅÍÍ¡ä»
2. ¡ÒÃÃÑ¡ÉÒàÊÃÔÁËÅѧ¼ÒµÑ´´ÇÂÇÔ¸·Õ Ò§ÂÒ (systemic adjuvant therapy) ໹¡ÒÃÃÑ¡ÉÒ´ÇÂà¤ÁպӺѴ
ÂÒµÒ¹ÎÍÃâÁ¹ËÃ×ÍÂÒ Targeted therapy â´ÂãËËÅѧ¨Ò¡¼»Ù Ç Âä´ÃºÑ ¡ÒÃÃÑ¡ÉÒ੾Òзդè Í× ¡ÒüҵѴÁÐàÃç§ÍÍ¡
价ѧé ËÁ´áÅÇ áÅм»Ù Ç ÂµÍ§äÁÁÃÕ ÍÂâä·Õàè ËÅ×ÍÍÂËÙ Åѧ¼ÒµÑ´
¨Ø´»ÃÐʧ¤¢Í§¡ÒÃÃÑ¡ÉÒ
à¾×èÍà¾ÔèÁÃÐÂÐàÇÅÒÃÍ´ªÕÇÔµâ´Â»ÅÍ´âä (Disease free survival) áÅÐà¾ÔèÁÃÐÂÐàÇÅÒ¡ÒÃÃÍ´ªÕÇÔµ
(overall survival)
»¨¨Ñ·Õèᾷµͧ»ÃÐàÁÔ¹áÅзÃÒº¡Í¹¡ÒõѴÊÔ¹ã¨ãË¡ÒÃÃÑ¡ÉÒ adjuvant
systemic therapy
1. Host factors ä´á¡ ÍÒÂØ, ÊÀÒÇлÃШÓà´×͹ (menopausal status), co-morbid diseases áÅÐ
performance status
2. Tumor factors ä´á¡ tumor size, tumor grading, lymphovascular invasion, surgical margins, lymph
node status áÅСÒÃÂÍÁ¾ÔàÈÉ·ÕÊè ӤѢͧÁÐàÃç§àµÒ¹Á·Õ¤è Çõͧ·ÃÒº¡Í¹¡ÒÃÃÑ¡ÉÒ¤×Í HR (hormone receptor
status«Ö§è ä´á¡ ER, PgR status) , HER2 áÅÐ Ki-67
¢Ñ¹
é µÍ¹·ÕÊè ͧ
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1. ¼»Ù Ç Â·Õäè Á¨Ó໹µÍ§ä´ÃºÑ ¡ÒÃÃÑ¡ÉÒàÊÃÔÁã´æËÅѧ¼ÒµÑ´
¢Íº§ªÕé ¼»Ù Ç Â·ÕÁè ¢Õ ¹Ò´¢Í§¡Í¹à¹×Íé §Í¡ </= 5 ÁÔÅÅÔàÁµÃ äÁÇÒ ¨ÐÁÕ»¨ ¨Ñº§ªÕ¡é ÒþÂҡóâä·Õè
äÁ´ÍÕ ¹×è ã´ËÃ×ÍäÁ
ÃдѺ¤Óá¹Ð¹Ó 2A
ÇÔ¸Õ¡ÒÃÃÑ¡ÉÒ´ÇÂÂÒµÒ¹ÎÍÃâÁ¹
¢Ö¹é ¡ÑºÀÒÇлÃШÓà´×͹¢Í§¼»Ù Ç Ââ´Âầ¼»Ù Ç Â໹ premenopausal áÅÐ postmenopausal women
µÒÁ¤Ó¨Ó¡Ñ´¤ÇÒÁ¢Í§ postmenopausal women (ÃÒÂÅÐàÍÕ´㹠appendix 1 ˹ҷÕè 62)
ÊÃØ»¤Óá¹Ð¹Ó㹡ÒÃàÅ×Í¡¡ÒÃÃÑ¡ÉÒàÊÃÔÁ·Ò§ÎÍÃâÁ¹ËÅѧ¼ÒµÑ´
1. ¼Ù Ë Ô § ·Õè ÂÑ § äÁ Ë Á´»ÃШÓà´× Í ¹ (Premenopausal women and/or
perimenopausal women) ¤Óá¹Ð¹Ó㹡ÒÃãË¡ÒÃÃÑ¡ÉÒàÊÃÔÁ´ÇÂÂÒµÒ¹ÎÍÃâÁ¹ã¹¼»Ù Ç Â
·ÕÂè §Ñ äÁËÁ´»ÃШÓà´×͹ (pre and perimenopausal women)
· ÂÒµÒ¹ÎÍÃâÁ¹·Õáè ¹Ð¹Ó໹¡ÒÃÃÑ¡ÉÒÁҵðҹ㹼»Ù Ç Â·Ø¡¤ÇÒÁàÊÕÂè §¤×Í tamoxifen
ÃдѺ¤Óá¹Ð¹Ó 1
· ÊÓËÃѺ¼»Ù Ç Â·ÕÁè ¢Õ Í ËÒÁ㹡ÒÃ㪠tamoxifen ËÃ×ÍäÁÊÒÁÒö·¹¼Å¢Ò§à¤Õ§¢Í§ tamoxifen
ä´ÍÒ¨ãªÇ¸Ô ¡Õ ÒÃ·Ó OFS (Ovarian function suppression) ·´á·¹
ÃдѺ¤Óá¹Ð¹Ó 1
· ÊÓËÃѺ¼Ù»Ç·ÕèÁÕ¤ÇÒÁàÊÕè§㹡ÒáÅѺ໹«éÓÊÙ§ á¾·ÂÍÒ¨¾Ô¨ÒóÒãË¡ÒÃÃÑ¡ÉÒ´Ç OFS
ÃÇÁ¡Ñº tamoxifen ÊÓËÃѺÃÐÂÐàÇÅҢͧ¡ÒÃ·Ó OFS äÁÁÃÕ ÐÂÐàÇÅÒÁҵðҹ·Õáè ¹¹Í¹â´Â
·ÑÇè ä»ãª»ÃÐÁÒ³ 2-3 »
ÃдѺ¤Óá¹Ð¹Ó 2B
· ÊÙµÃÂÒà¤ÁպӺѴ㹡ÒÃÃÑ¡ÉÒàÊÃÔÁËÅѧ¼ÒµÑ´
- á¹Ð¹ÓãËãªÊµÙ à classical CMF x 6 ËÃ×Í AC x 4 ËÃ×Í FAC x 6 ËÃ×Í FEC x 6 ËÃ×Í CEF x 6 Ãͺ
ÊÓËÃѺ¼»Ù Ç Â¤ÇÒÁàÊÕÂè §ã¹¡ÒáÅѺ໹«éÓ»Ò¹¡ÅÒ§
ÃдѺ¤Óá¹Ð¹Ó 1
- á¹Ð¹ÓãËãªÊµÙ à taxane- based chemotherapy ÃÇÁ¡Ñº anthracycline- based chemotherapy
੾ÒÐã¹¼»Ù Ç Â·ÕÁè ¤Õ ÇÒÁàÊÕÂè §ã¹¡ÒáÅѺ໹«éÓÊÙ§à·Ò¹Ñ¹é ä´á¡¼»Ù Ç Â·ÕÁè ¡Õ ÒáÃШÒÂä»ÂѧµÍÁ
¹éÓàËÅ×ͧÃÇÁ¡Ñºà¹×Íé §Í¡äÁµ´Ô µÑÇÃѺ·Ò§ÎÍÃâÁ¹ËÃ×ÍÁÕ¡ÒÃáÊ´§ÍÍ¡¢Í§ÂÕ¹ HER2
ÃдѺ¤Óá¹Ð¹Ó 1
- á¹Ð¹ÓãËãªÊٵà non-anthracycline, taxane-based 㹼ٻǷÕèÁÕ¤ÇÒÁàÊÕè§㹡ÒáÅѺ໹
«éÓ»Ò¹ ¡ÅÒ§¶Ö§ÊÙ§áÅÐÁÕ¢Í ËÒÁ㹡ÒÃãªÂÒ¡ÅÁØ anthracyclines
ÃдѺ¤Óá¹Ð¹Ó 1
- á¹Ð¹ÓãËãªÊµÙ à anthracycline-based chemotherapy , taxane-based chemotherapy ÃÇÁ¡Ñº
¡ÒÃ㪠trastuzumab ÊÓËÃѺ¼»Ù Ç Â HER2 positive ·Õäè ´ÃºÑ ¡ÒÃÃÑ¡ÉÒàÊÃÔÁ´ÇÂÂÒµÒ¹ HER2
ÃдѺ¤Óá¹Ð¹Ó 1
- ÃÐÂÐàÇÅҢͧ adjuvant chemotherapy á¹Ð¹ÓãËãªà»¹ÃÐÂÐàÇÅÒ 6 Ãͺ - 8 Ãͺ¡ÒÃÃÑ¡ÉÒ
(¢Ö¹é Í¡٠ºÑ ÊÙµÃ)
ÃдѺ¤Óá¹Ð¹Ó 1
- Sequence ÃÐËÇÒ§¡ÒÃÃÑ¡ÉÒ´Ç chemotherapy ¡Ñº¡ÒÃÃÑ¡ÉÒàÊÃÔÁª¹Ô´Í×è¹ á¹Ð¹ÓãËÃÑ¡ÉÒ
´Ç adjuvant chemotherapy ¡Í¹¨¹¤ÃºµÒÁ¨Ó¹Ç¹Ãͺ¡ÒÃÃÑ¡ÉÒ·Õ¡è Ó˹´áÅǨ֧µÒÁ´ÇÂ
adjuvant endocrine therapy
ÃдѺ¤Óá¹Ð¹Ó 1
5. AIs
ÁÕ¢Í º§ªÕàé ©¾Òм»Ù Ç Â postmenopausal women à·Ò¹Ñ¹é ÁÕ 3 ÇÔ¸ãÕ ¹¡ÒÃ㪠adjuvant AIs ´Ñ§µÍ仹Õé
· AIs 5 » (·´á·¹ tamoxifen) ÁÕ¡ÒÃÈÖ¡ÉÒ 2 ¡ÒÃÈÖ¡ÉÒ¤×Í ATAC study(5) à»ÃÕºà·Õº¡ÒÃãª
anastrozole 5 »¡ºÑ ¡ÅÁØ ·Õãè ª tamoxifen 5 » àÁ×Íè µÔ´µÒÁ¼Å¡ÒÃÈÖ¡ÉÒ¨¹¶Ö§·Õè 100 à´×͹ ¾ºÇÒ¡ÅÁØ ·Õãè ª anastrozole
5 »ÁÕ DFS ´Õ¡ÇÒ¡ÅØÁ·Õè㪠tamoxifen 5 »ÃÍÂÅÐ 4.8 áÅÐÁÕ HR = 0.76 «Ö觴աÇÒÍÂÒ§ÁÕ¹ÑÂÊӤѷҧʶԵÔ
áÅй͡¨Ò¡¹Ñ¹é ¡ÅÁØ ·Õäè ´ anastrozole 5 »Â§Ñ Å´ÍѵÃÒ¡ÒÃà¡Ô´ contralateral breast cancer ä´ÍÂÒ§ÁÕ¹ÂÑ ÊÓ¤Ñâ´ÂÁÕ
HR = 0.68 áµäÁÁ¤Õ ÇÒÁᵡµÒ§ã¹á§¢Í§ overall survival ¡ÒÃÈÖ¡ÉÒ·ÕÊè ͧ¤×Í BIG 1-98(6) 㹡ÒÃÈÖ¡ÉÒ ¹ÕÁé ¡Õ ÅÁØ ·Õãè ª
tamoxifen 5 »à»¹¡ÅÁØ ¤Çº¤ØÁáÅÐÁÕ¡ÅÁØ ·Õãè ª letrozole 5 » ¾ºÇÒàÁ×Íè µÔ´µÒÁ¡ÒÃÈÖ¡ÉÒ·Õè 76 à´×͹ ¡ÅÁØ ·Õäè ´ÃºÑ
letrozole 5 »ÁÕ DFS ´Õ¡ÇÒÍÂÒ§ÁÕ¹ÂÑ ÊӤѷҧʶԵàÔ ª¹à´ÕÂǡѹ â´ÂÁÕ HR = 0.88 áµäÁÁ¤Õ ÇÒÁᵡµÒ§ã¹á§¢Í§
overall survival હà´ÕÂǡѹ
· Sequential treatment ÇÔ¸Õ¹Õé¤×ÍãËÂÒµÑÇã´µÑÇ˹Ö觡͹㹪ǧ 2-3 »áááÅÇÊÅѺÁÒ໹ÂÒÍÕ¡
ª¹Ô´Ë¹Ö§è ¨¹¤Ãº 5 » ÁÕÊͧÇÔ¸ÂÕ Í Â¤×Í
- Tamoxifen 2-3 » ¨Ò¡¹Ñ¹é ÊÅѺÁÒ໹ AIs ÍÕ¡ 2-3 »¨¹¤Ãº 5 »
¡ÒÃÈÖ¡ÉÒÊӤѷÕàè »ÃÕºà·Õº¡ÒÃãªÅ¡Ñ ɳйÕàé ·Õº¡Ñº¡ÒÃ㪠AIs µÅÍ´ 5 »·àÕè ÃÔÁè ÊÁØ ¼»Ù Ç Â
µÑ§é ᵵ͹àÃÔÁè µ¹¤×Í BIG 1-98 study â´Â¡ÒÃÇÔà¤ÃÒÐË¢Í ÁÙŢͧ STA (sequential treatment
analysis) ·ÕèÁÕ¡ÒõԴµÒÁ¼Ù»Ç 71 à´×͹ ¾ºÇÒäÁÁÕ¤ÇÒÁᵡµÒ§¡Ñ¹ÍÂÒ§ÁÕ¹ÑÂÊӤѷҧ
ʶԵÔà·Õº¡Ñº¡ÒÃ㪠letrozole 5 » â´ÂÁÕ HR for DFS, OS and TTDR ·Õè 1.05, 1.13 áÅÐ 1.22
ÍÂÒ§äáçµÒÁàÁ×Íè ÇÔà¤ÃÒÐ˨Óṡ¼»Ù Ç Â໹¡ÅÁØ ·ÕÁè ËÕ Ã×ÍäÁÁ¡Õ ÒáÃШÒÂä»ÂѧµÍÁ¹éÓàËÅ×ͧ
¾ºÇÒ¶Ò໹¼Ù»Ç·ÕèäÁÁÕ¡ÒáÃШÒÂä»ÂѧµÍÁ¹éÓàËÅ×ͧÍѵÃÒ¡ÒáÅѺ໹«éÓäÁÁÕ¤ÇÒÁ
ᵡµÒ§¡Ñ¹ÁÒ¡¹Ñ¡ ᵶÒ໹¡ÅØÁ·ÕèÁÕ¡ÒáÃШÒÂä»ÂѧµÍÁ¹éÓàËÅ×ͧ ÍѵÃÒ¡ÒáÅѺ໹«éÓ
·Õè 2 »áá 4.7% à·Õº¡Ñº 7.9% áÅзÕè 5 »ÍÂÙ·Õè 12.4% áÅÐ 14.7% «Öè§ÊÙ§¡ÇÒ㹡ÅØÁ·Õèä´ÃѺ
tamoxifen ¡Í¹à·Õº¡Ñº¡ÒÃä´ÃѺ letrozole ·Ñé§ 5 » ÍÂÒ§äáçµÒÁÁÕÍա˹Ö觡ÒÃÈÖ¡ÉÒ·Õè
à»ÃÕºà·Õºã¹Åѡɳйդé Í× TEAM study(7) «Ö§è à»ÃÕºà·Õº¼»Ù Ç Â·Õäè ´ÃºÑ exemestane «Ö§è ໹
steroidal AI µÅÍ´ 5 »¡ºÑ ÍÕ¡¡ÅÁØ ·Õäè ´ÃºÑ tamoxifen ¡Í¹ ¼Å¡ÒÃÈÖ¡ÉÒ·Õè 5 »¾ºÇÒäÁÁ¤Õ ÇÒÁ
ᵡµÒ§¡Ñ¹ã¹á§¢Í§ DFS â´ÂÁÕ HR = 0.97 áÅÐ overall survival â´ÂÁÕ HR = 1.0
- AIs ¡Í¹ 2-3 »¨Ò¡¹Ñ¹é ¡ÅѺÁÒ໹ tamoxifen ¨¹¤Ãº 5 »
ÁÕà¾Õ§¡ÒÃÈÖ¡ÉÒà´ÕÂÇ·ÕÈè ¡Ö ÉÒ¶Ö§ÇÔ¸¹Õ ¤Õé Í× BIG 1-98 study ¾ºÇÒàÁ×Íè à·Õº¡Ñº¡ÒÃãË letrozol
µÅÍ´ 5 » ¡ÒÃ㪠letrozole ¡Í¹ 2 »áÅÇ¡ÅѺÁÒ໹ tamoxifen ¨¹¤Ãº 5 »äÁÁÕ¤ÇÒÁ
ᵡµÒ§¡Ñ¹ã¹á§¢Í§ DFS, OS áÅÐ TTDR áÅÐàÁ×èÍ´ÙÍѵÃÒ¡ÒáÅѺ໹«éÓ·Ñ駷Õè 2 áÅÐ 5
»·Ñé§ã¹¼Ù»Ç¡ÅØÁ·ÕèÁÕËÃ×ÍäÁÁÕ¡ÒÃá¾Ã¡ÃШÒÂÁÒÂѧµÍÁ¹éÓàËÅ×ͧ¡çäÁ¾º¤ÇÒÁᵡµÒ§
હà´ÕÂǡѹ áµÍÂÒ§äáçµÒÁ໹à¾Õ§¡ÒÃÈÖ¡ÉÒà´ÕÂÇà·Ò¹Ñ¹é ·Õµè ͺ¤Ó¶ÒÁ¹Õé
· Extended AIs ¤×ÍãËÂÒ tamoxifen 5 »áÅжҼٻÇÂÂѧäÁÁÕ¡ÒáÅѺ໹«éÓáÅÐÍÂÙã¹ÇÑÂËÁ´
»ÃШÓà´×͹¡çãËÂÒ AIs µÍÍÕ¡ 5 » ÃÇÁÃÐÂÐàÇÅÒ¡ÒÃãËÂҷѧé ËÁ´ 10 »
¡ÒÃÈÖ¡ÉÒÊӤѤ×Í MA 17(8) à»ÃÕºà·ÕºÃÐËÇÒ§¡ÅØÁ·Õèä´ÃѺ tamoxifen 5 »«Ö觶×ÍÇÒ໹¡ÅØÁ
¤Çº¤ØÁ¡Ñº¡ÅÁØ ÈÖ¡ÉÒ¤×Íä´ÃºÑ ÂÒ tamoxifen 5 »áÅǵÒÁ´Ç letrozole ÍÕ¡ 5 » ¼Å¡ÒÃÈÖ¡ÉÒ¾ºÇÒ¡ÅÁØ ·Õäè ´ÃºÑ letrozole
µÍÁÕ DFS ·Õè´Õ¡ÇÒÍÂÒ§ÁÕ¹ÑÂÊÓ¤Ñ HR = 0.58 áÅÐ㹼ٻǷÕèÁÕ¡ÒáÃШÒÂä»ÂѧµÍÁ¹éÓàËÅ×ͧÁÕ OS ´Õ¡ÇÒ
ÍÂÒ§ÁÕ¹ÂÑ ÊӤѷҧʶԵàÔ ª¹à´ÕÂǡѹâ´ÂÁÕ HR = 0.61
Doxorubicin 60 mg/m2 D1
Cyclophosphamide 600 mg/m2 D1 ·Ø¡ 21 Çѹ 4 Ãͺ
3. FAC x 6
5-FU 500 mg/m2 D1
Doxorubicin 50 mg/m2 D1
Cyclophosphamide 500 mg/m2 D1 ·Ø¡ 21 Çѹ 6 Ãͺ
4. FE(100)C x 6(17)
5-FU 500 mg/m2 D1
Epirubicin 100 mg/m2 D1
Cyclophosphamide 500 mg/m2 D1 ·Ø¡ 21 Çѹ 6 Ãͺ
3. ¡ÒÃÈÖ¡ÉÒ BCIRG 006(23) ¾ºÇÒ¡ÅÁØ ·Õäè ´ trastuzumab ໹¡ÒÃÃÑ¡ÉÒàÊÃÔÁ äÁÇÒ ¨ÐãªÃÇ Á¡ÑºÊÙµÃÂÒ
·ÕèÁÕËÃ×ÍäÁÁÕ anthracyclines ໹Êǹ»ÃСͺ ÃÒ§ҹËÅѧµÔ´µÒÁ¼Å¡ÒÃÃÑ¡ÉÒ 36 à´×͹ ¾ºÇÒ¡ÅØÁ·Õèä´
trastuzumab ÁÕ DFSáÅÐ OS ·Õ´è ¡Õ ÇÒ¡ÅÁØ ·Õäè Áä´ÃºÑ ÂÒÍÂÒ§ÁÕ¹ÂÑ ÊÓ¤Ñ·Ò§Ê¶ÔµÔ (absolute benefit 5-6%)
4. FinHer trial ä´È¡Ö ÉÒ¡ÒÃ㪠Trastuzumab ໹àÇÅÒ 9 ÊÑ»´ÒË ÃÇÁ¡Ñº docetaxel ËÃ×Í vinorelbine
µÔ´µÒÁ´Ç FEC ¨Ó¹Ç¹ 3 Ãͺ â´ÂäÁÁÕ Trastuzumab ã¹¼»Ù Ç ÂÁÐàÃç§àµÒ¹ÁÃÐÂÐáá·ÕÁè Õ HER-2 ໹¼ÅºÇ¡
·Ñé§ÁÕáÅÐäÁÁÕ¡ÒáÃШÒÂä»ÂѧµÍÁ¹éÓàËÅ×ͧ¨Ò¡¡ÒõԴµÒÁ໹àÇÅÒ 36 à´×͹ ¾ºÇÒ¼Ù»ÇÂ㹡ÅØÁ·Õèä´ÃѺ
Trastuzumab ÁÕÍѵÃÒ¡ÒÃÍÂÙÃÍ´â´Â»ÃÒȨҡâä (RFS) ´Õ¢Ö鹡ÇÒ¡ÅØÁ·ÕèäÁä´ÃѺÍÂÒ§ÁÕ¹ÑÂÊÓ¤Ñ (89 % áÅÐ
78 % µÒÁÅӴѺ) áµäÁÁ¤Õ ÇÒÁᵡµÒ§¢Í§ÃÐÂÐàÇÅÒ¡ÒÃÍÂÃÙ Í´ (OS)
à¹×Íè §¨Ò¡¡ÒÃ㪠Trastuzumab ÁռŢҧà¤Õ§·ÕÊè Ó¤Ñ ¤×Í ÀÒÇÐËÑÇã¨ÅÁàËÅÇ ¨Ö§µÍ§ÁÕ¡ÒÃà½ÒµÔ´µÒÁ
¡Ò÷ӧҹ¢Í§ËÑÇã¨à»¹ÃÐÂÐã¹ÃÐËÇÒ§¡ÒÃÃÑ¡ÉÒ ¨Ò¡¡ÒÃÇÔà¤ÃÒÐ˼ÅÃÇÁ¢Í§¡ÒÃÈÖ¡ÉÒ NSABP B31 áÅÐ
NCCTG 9831 ¾ºÇÒ ã¹¡ÅÁØ ·Õäè ´ Trastuzumab ¾ÃÍÁ¡Ñº paclitaxel ÁÕÀÒÇÐËÑÇã¨ÅÁàËÅÇ 51 ÃÒ 㹢³Ð·ÕÁè àÕ ¾Õ§
5 ÃÒÂ㹡ÅØÁ¤Çº¤ØÁ 㹡ÒÃÈÖ¡ÉÒ HERA ¾ºÀÒÇÐËÑÇã¨ÅÁàËÅÇ 9 ÃÒ ¨Ò¡ 1,677 ÃÒ ·Õèä´ Trastuzumab
µÒÁËÅѧà¤ÁպӺѴ áÅÐäÁ¾ºÀÒÇйÕé㹡ÅØÁ¤Çº¤ØÁ ÍغѵԡÒó¢Í§ÀÒÇÐËÑÇã¨ÅÁàËÅÇã¹ HERA ¹Í¡ÇÒ
NSABP B31 áÅÐ NCCTG 9831 ÍҨ໹à¾ÃÒСÒÃãË Trastuzumab µÒÁËÅѧà¤ÁպӺѴ ÁÔä´ã˾ÃÍÁ¡Ñ¹
áÅм»Ù Ç Â ·Õàè ¢ÒÃÇÁµÍ§ÁÕ LVEF ÁÒ¡¡ÇÒ 55 % á·¹·Õ¨è Ð໹ 50 % 㹡ÒÃÈÖ¡ÉÒÍ×¹è
â´ÂÊÃØ»¡ÒÃ㪠trastuzumab ໹¡ÒÃÃÑ¡ÉÒàÊÃÔÁã¹¼»Ù Ç ÂÁÐàÃç§àµÒ¹ÁÃÐÂÐáá·ÕÁè Õ HER2 positive
¾ºÇÒÂѧ¤§ãËÃÐÂÐàÇÅÒÃÍ´ªÕÇÔµâ´Â»ÃÒȨҡâäáÅÐÃÐÂÐàÇÅÒÃÍ´ªÕǵԴբÖé¹ÍÂÒ§ÁÕ¹ÑÂÊӤѷҧʶԵÔ
áµÍÂÒ§äáçµÒÁÂѧÁÕºÒ§¨Ø´·ÕÂè §Ñ äÁÁ¤Õ ӵͺ·Õªè ´Ñ ਹ હÃÐÂÐàÇÅÒ·Õàè ËÁÒÐÊÁ㹡ÒÃãË trastuzumab ÃÐËÇÒ§
1 ËÃ×Í 2 » ËÃ×ÍÃÐÂÐÊÑ¹é ¡ÇÒ¹Õé ¡ÒÃãËÂÒ trastuzumab ÃÇÁ¡ÑºÂÒ¡ÅÁØ taxanes ËÃ×ÍãªËÅѧ¨Ò¡ÃÑ¡ÉÒ´ÇÂà¤ÁպӺѴ
¨ºÊÔ¹é áÅÇ ¹Í¡¨Ò¡¹Ñ¹é ¡ÒÃÃÑ¡ÉÒ´Ç trastuzumab ÁռŢҧà¤Õ§µÍËÑÇã¨à¾ÔÁè ÁÒ¡¢Ö¹é
References
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1. ¤ÇÃãªÎÍÃâÁ¹ã¹¡ÒÃÃÑ¡ÉÒ㹡óշÕè
· ÁռŠEstrogen receptor (ER) áÅÐ / ËÃ×Í Progesterone receptor (PgR) ໹¼ÅºÇ¡ áÅÐÁÐàÃç§Âѧ
äÁá¾Ã¡ÃШÒÂä»ÍÇÑÂÇÐÀÒÂã¹ «Ö§è ÍÒ¨·Óã˼»Ù Ç Â¶Ö§á¡ªÇÕ µÔ ã¹àÇÅÒÍѹÃÇ´àÃçÇ àª¹ extensive liver metastasis
ËÃ×Í pulmonary lymphangitic metastasis ËÃ×Í brain metastasis ໹µ¹
· ¡Ã³Õ·äÕè Á·ÃÒº¼Å ER áÅÐ PgR ¨Ð¾Ô¨ÒóÒãËÎÍÃâÁ¹àÁ×Í è
- ÃÐÂлÅÍ´âä (disease-free interval) ¹Ò¹à¡Ô¹ 2 »
- µÓá˹§¢Í§¡ÒÃá¾Ã¡ÃШÒÂäÁ·Óã˼»Ù Ç ÂàÊÕªÕÇµÔ â´ÂÃÇ´àÃçÇ àª¹ µÍÁ¹éÓàËÅ×ͧ à¹×Íé àÂ×Íè
Í͹ (soft tissue) ¼ÔÇ˹ѧ ¡Ãд١ àÂ×Íè ËÁØ »Í´ ໹µ¹
- ÍÒÂØÁÒ¡¡ÇÒ 50 » ËÃ×Í ÇÑÂËÁ´»ÃШÓà´×͹
- à¤ÂµÍºÊ¹Í§µÍ¡ÒÃÃÑ¡ÉÒ´ÇÂÎÍÃâÁ¹Áҡ͹
ÃдѺ¤Óá¹Ð¹Ó 2A
¡ÒõͺʹͧµÍÎÍÃâÁ¹¨Ð¢Ö¹é Í¡٠ºÑ ¼Å¢Í§ ER áÅÐ/ËÃ×ÍPgR(2) â´Â¼»Ù Ç Â·ÕÁè ·Õ §Ñé ER áÅÐ
PgR ໹¼ÅºÇ¡ ÁÕâÍ¡ÒʵͺʹͧµÍÎÍÃâÁ¹»ÃÐÁÒ³ÃÍÂÅÐ 50-70 㹡óշÕè ER ËÃ×Í PgR ໹¼ÅºÇ¡ÁÕ
¡Òõͺʹͧ ÃÍÂÅÐ 33 áµã¹¡Ã³Õ·Õè ER áÅÐ PgR ໹¼Åź ÁÕ¡Òõͺʹͧà¾Õ§ÃÍÂÅÐ 5-10 à·Ò¹Ñ¹é ¡ÒÃ
µÍºÊ¹Í§µÍÎÍÃâÁ¹·Ñ§é ã¹ÇÑÂà¨ÃԾѹ¸áØ ÅÐÇÑÂËÁ´»ÃШÓà´×͹ÍÂãÙ ¹à¡³±ã¡Åà¤Õ§¡Ñ¹
3. äÁá¹Ð¹ÓãËãªÎÍÃâÁ¹¾ÃÍÁ¡Ñºà¤ÁպӺѴ㹡ÒÃÃÑ¡ÉÒÁÐàÃç§àµÒ¹ÁÃÐÂÐ
á¾Ã¡ÃШÒÂ
ÃдѺ¤Óá¹Ð¹Ó 1
¨Ò¡¢ÍÁÙÅ¡ÒÃÈÖ¡ÉÒẺ Randomized trials áÅÐ overview analysis ¾ºÇÒ¡ÒÃãªÎÍÃâÁ¹¾ÃÍÁ¡Ñº
à¤ÁպӺѴ ÍÒ¨ÁÕ¡Òõͺʹͧ·Õèà¾ÔèÁ¢Öé¹ áµäÁ·Óã˼ٻÇÂÁÕªÕÇÔµÂ×¹ÂÒÇ¢Öé¹àÁ×èÍà·Õº¡Ñº¡ÒÃãªÎÍÃâÁ¹à¾Õ§
ÍÂÒ§à´ÕÂÇ(3,4,11-16)
5. ª¹Ô´¢Í§ÎÍÃâÁ¹·Õãè ª : ¢Ö¹
é Í¡٠ºÑ ÇÒ¼»Ù Ç Â໹ÇÑ¡͹ËÁ´»ÃШÓà´×͹ ËÃ×Í
ÇÑÂËÅѧËÁ´»ÃШÓà´×͹
5.1 ¼»Ù Ç ÂÇÑ¡͹ËÁ´»ÃШÓà´×͹ (µÒÁ¤Ó¨Ó¡Ñ´¤ÇÒÁ¢Í§¡ÒÃËÁ´»ÃШÓà´×͹ã¹á¹Ç·Ò§¢Í§
¼»Ù Ç ÂÃÐÂÐáá)
· ÎÍÃâÁ¹µÑÇáá·Õ¤ è ÇÃ㪠Tamoxifen ËÃ×Í ovarian ablation
ÃдѺ¤Óá¹Ð¹Ó 1
ã¹Í´Õµá¹Ð¹ÓãË·Ó ovarian ablation (bilateral oophorectomy) ໹¡ÒÃÃÑ¡ÉÒËÅÑ¡ ¾ºÇÒÁÕ¡ÒÃ
µÍºÊ¹Í§ÍÂãÙ ¹ªÇ§ÃÍÂÅÐ15-56 áÅÐÁÕ¡Òõͺʹͧâ´Âà©ÅÕÂè 9-15 à´×͹(19) ¡ÒÃ·Ó bilateral oophorectomy
ÍÒ¨ãªÇԸռҵѴ ©ÒÂáʧ ËÃ×ÍãËÂÒ¡ÅØÁ LHRH agonist હ leuprolide ËÃ×Í goserelin(20) ã¹ÃÐÂÐËÅѧ¹ÔÂÁ
ãË Tamoxifen ໹¡ÒÃÃÑ¡ÉÒËÅÑ¡ÁÒ¡¢Öé¹ à¹×èͧ¨Ò¡ÁÕÃÒ§ҹÇÒÁÕ»ÃÐÊÔ·¸ÔÀÒ¾à·Ò¡Ñº¡ÒÃ·Ó bilateral oopho-
rectomy(21,22)
¨Ð¾Ô¨ÒóÒ㪠tamoxifen 㹡óշ¼Õè »Ù Ç ÂäÁà¤Âä´ tamoxifen Áҡ͹ËÃ×Íà¤Âä´ tamoxifen
໹¡ÒÃÃÑ¡ÉÒàÊÃÔÁÀÒÂËÅѧ¼ÒµÑ´áÅÇËÂØ´ä»áÅǹҹà¡Ô¹ 1 »¢¹Öé ä»
· ÎÍÃâÁ¹µÑÇ·ÕÊ è ͧ·Õ¤è ÇÃ㪠¡Ã³Õ·âÕè äÅØ¡ÅÒÁÁÒ¡¢Ö¹é ËÅѧ¨Ò¡·ÕÁè ¡Õ ÒõͺʹͧµÍÎÍÃâÁ¹
µÑÇááÃÐÂÐË¹Ö§è ¤×Í ovarian ablation ËÃ×Í tamoxifen ËÃ×Í progestin
ÃдѺ¤Óá¹Ð¹Ó 2A
¡Ã³Õ·¼Õè »Ù Ç Âà¤Â㪠tamoxifen ໹µÑÇáá ÍÒ¨¾Ô¨ÒóÒ㪠ovarian ablation ËÃ×ͶҼ»Ù Ç Âà¤Âãª
ovarian ablation ໹µÑÇáá¡ç¾¨Ô ÒÃ³Ò ãË tamoxifen ໹µÑÇ·ÕÊè Í(23,24) 㹡óշ¼Õè »Ù Ç Â»®Ôàʸ ovarian ablation
ÍÒ¨¾Ô¨ÒóÒãË progestin ( megestrol acetate ËÃ×Í medroxyprogesterone acetate )
6. ¢¹Ò´¢Í§ÎÍÃâÁ¹áµÅЪ¹Ô´·Õáè ¹Ð¹ÓãËãª
Antiestrogen
Tamoxifen 20 mg/day per oral
Fulvestrant 250 mg intramuscular q 4 weeks
LHRH agonist
Leuprolide 3.75 mg subcutaneous q 4 weeks
Goserelin 3.6 mg subcutaneous q 4 wks
Aromatase inhibitors
Anastrozole 1 mg/day per oral
Letrozole 2.5 mg/day per oral
Exemestane 25 mg/day per oral
Progestin
Megestrol acetate 160 mg/day per oral
Medroxyprogesterone acetate 1000 mg/day per oral
¡ÒÃãªÂÒà¤ÁպӺѴã¹ÁÐàÃç§àµÒ¹ÁÃÐÂÐá¾Ã¡ÃШÒÂ
¢Íº§ªÕé
1. ¼»Ù Ç Â·ÕÁè ¼Õ Å ER áÅÐ PgR ໹¼Åź
2. ¼»Ù Ç Â·Õâè äÅØ¡ÅÒÁÃÐËÇÒ§¡ÒÃÃÑ¡ÉÒ´ÇÂÂÒÎÍÃâÁ¹ËÃ×Í´×Íé µÍÎÍÃâÁ¹
3. ¼»Ù Ç Â·Õâè äá¾Ã¡ÃШÒÂÍÂÒ§ÃÇ´àÃçÇ á¾Ã¡ÃШÒÂä»ÂѧÍÇÑÂÇÐÊÓ¤ÑáÅÐÍÒ¨ÁÕÍ¹Ñ µÃÒ¶֧ªÕǵÔ
હµÑº »Í´ ÊÁͧ໹µ¹
ÃдѺ¤Óá¹Ð¹Ó 1
ÂѧäÁÁ¡Õ ÒÃÈÖ¡ÉÒẺÊÁØ à»ÃÕºà·Õº ¡ÅÁØ ·Õãè Ëà¤ÁպӺѴ¡Ñº¡ÅÁØ ·ÕÃè ¡Ñ ÉÒµÒÁÍÒ¡Òà áµÁ¡Õ ÒÃÈÖ¡ÉÒ
Ẻ metaanalysis áÅÐ population-based cohort ·Õºè § ÇÒà¤ÁպӺѴªÇÂã軂 §ªÕÇµÔ à¾ÔÁè ¢Ö¹é »ÃÐÁÒ³ 6-9 à´×͹(42,43)
ª¹Ô´¢Í§à¤ÁպӺѴ
1. ¡Ã³Õ¢Í§ÂÒÊÙµÃáá á¹Ð¹ÓãË㪠classical CMF ËÃ×Í anthracycline-containing regimen હ
FAC, AC, EC, ËÃ×Í FEC ໹µ¹ â´ÂÁÕËÅÑ¡¡ÒÃàÅ×Í¡ÊÙµÃÂҴѧ¹Õé
· ¡Ã³Õ·¼Õè »
Ù Ç ÂäÁà¤Âä´ÃºÑ ¡ÒÃÃÑ¡ÉÒàÊÃÔÁËÅѧ¼ÒµÑ´´ÇÂÂÒà¤ÁպӺѴÁҡ͹ á¹Ð¹ÓãË㪠classical
CMF ËÃ×Í anthracycline-containing regimen હ FAC, AC, EC, ËÃ×Í FEC ໹µ¹
· ¡Ã³Õ ·Õè ¼Ù » Ç Âà¤Âä´ ÃÑ º ¡ÒÃÃÑ ¡ ÉÒàÊÃÔ Á ËÅÑ § ¼ Ò µÑ ´ ´ Ç ÂÂÒà¤ÁÕ ºÓºÑ ´ ÁÒ¡ Í ¹¹Ò¹à¡Ô ¹ 1»
á¹Ð¹ÓãËãªÂÒà¤ÁպӺѴªØ´à´ÔÁä´â´Â੾ÒÐ classical CMF 㹡óբͧ anthracycline-containing regimen
á¹Ð¹ÓãËãªÂÒà¤ÁպӺѴªØ´ãËÁá·¹
· ¡Ã³Õ·Õè¼Ù»ÇÂà¤Âä´ÃѺ¡ÒÃÃÑ¡ÉÒàÊÃÔÁËÅѧ¼ÒµÑ´´ÇÂÂÒà¤ÁպӺѴÁҡ͹¹Ò¹¹Í¡ÇÒ 1 »
á¹Ð¹ÓãËãªÂÒà¤ÁպӺѴªØ´ãËÁá·¹
ÃдѺ¤Óá¹Ð¹Ó 1
ÁÕ¡ÒÃÈÖ¡ÉÒẺ metaanalysis ¾ºÇÒ¡ÒÃãªÂÒà¤ÁպӺѴËÅÒµÑǾÃÍÁ¡Ñ¹¨Ðä´»ÃÐÊÔ·¸ÔÀÒ¾´Õ¡ÇÒ
¡ÒÃãªÂÒà¤ÁպӺѴà¾Õ§µÑÇà´ÕÂÇâ´ÂÁÕ relative hazard ratio (HR) ¢Í§ªÇ§ªÕÇԵ໹ 0.70 (95% confidence
intervals (CIs) 0.59-0.84)(4) 㹡óբͧ CMF¡ÒÃ㪠classical CMF (㪠cyclophosphamide Ẻ¡Ô¹)
àÁ×Íè à·Õº¡Ñº¡ÒÃ㪠modified CMF ( intravenous 3-week CMF) ¾ºÇÒ¡ÒÃ㪠classical CMF ÁÕ¡Òõͺʹͧ·Õ´è ¡Õ ÇÒ
(48% ¡Ñº 29%; p = 0.003) áÅÐÁÕªÇ §ªÕÇµÔ ·Õ´è ¡Õ ÇÒ (17 ¡Ñº 12 à´×͹; p = 0.016) ¡ÒÃ㪠modified CMF (55)
anthracycline-containing regimen ÁÕ¡Òõͺʹͧ·Õ´è ¡Õ ÇÒáÅÐÁÕªÇ §ªÕÇµÔ ·Õ´è ¡Õ ÇÒ CMF àÅ硹ÍÂâ´ÂÁÕ
relative HR 0.89 (95% CIs 0.82-0.97) (4) áµÁ¼Õ Å¢Ò§à¤Õ§ÁÒ¡¡ÇÒ CMF ´Ç ÍÂÒ§äáçµÒÁ¢ÍÁÙŢͧ¡ÒÃÈÖ¡ÉÒ
ä´ÃÇÁ·Ñ§é classical CMF áÅÐ modified CMF
ã¹»¨¨Øº¹Ñ ÁÕ¢Í ÁÙžºÇÒ¡ÒÃ㪠taxanes (docetaxel ËÃ×Í paclitaxel) ÃÇÁ¡Ñº anthracycline (doxorubi-
cin ËÃ×Í epirubicin) ÁÕ¡Òõͺʹͧ·Õè´Õ¡ÇÒ¡ÒÃ㪠Anthracycline ÃÇÁ¡Ñº cyclophosphamide áµÂѧäÁÁÕ
¢ÍÁÙŪѴਹÇÒ ·Óã軂 §ªÕÇµÔ Â×¹ÂÒÇ¢Ö¹é (56-62) ¨Ö§ÂѧäÁá¹Ð¹ÓãËãªà»¹ÂҪشáá㹢³Ð¹Õé
· ¡Ã³Õ¢Í§ÂÒÊٵ÷ÕÊ è ͧàÁ×Íè âäÅØ¡ÅÒÁËÅѧãËÂҪشáá
1. ¡Ã³Õ·àÕè ¤Âä´ anthracycline-containing regimen ໹ÂÒÊÙµÃáá
á¹Ð¹ÓãË㪠taxanes (docetaxel ËÃ×Í paclitaxel)
ÃдѺ¤Óá¹Ð¹Ó 1
2. ¡ÒÃãªÂÒµÑÇÍ×¹è ·Õäè Á㪠taxane હ vinorelbine, capecitabine, gemcitabine ËÃ×Í CMF
ÃдѺ¤Óá¹Ð¹Ó 2A
· ¡Ã³Õ·ãÕè ª CMF ໹ÂÒÊÙµÃáá
á¹Ð¹ÓãË㪠anthracycline-containing regimen ໹ÂÒÊٵ÷ÕèÊͧ áÅǤ;ԨÒóÒãª
ÂÒµÑÇÍ×¹è ´Ñ§·Õ¡è ÅÒÇäÇã¹ 2 µÍä»
ÃдѺ¤Óá¹Ð¹Ó 1
äÁÁ¢Õ Í ÁÙÅà»ÃÕºà·ÕºÃÐËÇÒ§¡ÅÁØ ·Õãè ËÂÒà¤ÁպӺѴ¡Ñº¡ÅÁØ ·ÕÃè ¡Ñ ÉÒµÒÁÍÒ¡Òà áµÁ¢Õ Í ÁÙÅà»ÃÕºà·Õº
ÃÐËÇÒ§ ÂÒãËÁ㹡ÅÁØ taxane áÅÐ vinorelbine à·Õº¡ÑºÂÒà¡Ò·Õàè ¤Âãªã¹Í´Õµ¾ºÇÒÊÒÁÒö·ÓãËÁªÕ ÇÕ µÔ Â×¹ÂÒÇ
¢Öé¹(50,63-66) ÁÕÃÒ§ҹà»ÃÕºà·ÕºÃÐËÇÒ§¡ÒÃ㪠docetaxel ÃÇÁ¡Ñº capecitabine ¡Ñº docetaxel à¾Õ§µÑÇà´ÕÂÇ
ã¹¼»Ù Ç Â·Õàè ¤Âä´ÃºÑ anthracycline Áҡ͹ ¾ºÇÒ¡ÒÃ㪠docetaxel ÃÇÁ¡Ñº capecitabine ·ÓãËÁªÕ Ç §ªÕÇµÔ à¾ÔÁè ÁÒ¡¢Ö¹é
(14.5 à´×͹ ¡Ñº 11.5 à´×͹; p=0.0126) àÁ×Íè à·Õº¡Ñº docetaxel à¾Õ§µÑÇà´ÕÂÇ(54) ÁÕÃÒ§ҹà»ÃÕºà·ÕºÃÐËÇÒ§¡ÒÃãª
paclitaxel ÃÇÁ¡Ñº gemcitabine ¡Ñº pacllitaxel à¾Õ§µÑÇà´ÕÂÇ ã¹¼»Ù Ç Â·Õàè ¤Âä´ÃºÑ anthracycline Áҡ͹ ¾ºÇÒ¡ÒÃãª
paclitaxel ÃÇÁ¡Ñº gemcitabine ·ÓãËÁÕ progression-free survival áÅÐ overall survival à¾ÔÁè ÁÒ¡¢Ö¹é àÁ×Íè à·Õº¡Ñº
paclitaxel à¾Õ§µÑÇà´ÕÂÇ(79,82) ÁÕÃÒ§ҹ¡ÒÃ㪠capecitabine, gemcitabine áÅÐ Vinorelbine 㹼ٻǷÕèà¤Âä´
anthracycline Áҡ͹ áÅǾºÇÒÁÕ¡Òõͺʹͧ(80)
· ¡Ã³Õ¢Í§ÂÒÊٵ÷ÕÊ è ÒÁàÁ×Íè âäÅØ¡ÅÒÁËÅѧãËÂÒÊٵ÷ÕÊè ͧ
á¹Ð¹ÓãË㪠capecitabine ËÃ×Í vinorelbine ËÃ×Í gemcitabine 㹡óշÕèà¤Âä´ taxane
໹ÂÒÊٵ÷ÕÊè ͧ ËÃ×;ԨÒóÒà¢Òâ¤Ã§¡ÒÃÈÖ¡ÉÒ (clinical trial) ËÃ×ÍÃÑ¡ÉÒµÒÁÍÒ¡ÒÃáÅÇᵡóÕ
ÃдѺ¤Óá¹Ð¹Ó 2A
ÁÕ¡ÒÃÈÖ¡ÉÒẺ Phase II ¢Í§ capecitabine 㹼ٻǷÕè´×éÍµÍ anthracycline áÅÐ taxane ¾ºÇÒ
ÁÕ¡Òõͺʹͧ 20%(67) ¹Í¡¨Ò¡¹ÕÁé ¡Õ ÒÃÈÖ¡ÉÒẺ Phase II ¢Í§ vinorelbine áÅÐ gemcitabine ã¹¼»Ù Ç Â·Õ´è Í×é µÍ
taxane áÅǾºÇÒÁÕ¡Òõͺʹͧહ¡Ñ¹(68,69) ÁÕ¡ÒÃÈÖ¡ÉÒẺ randomized phase III ¢Í§¡ÒÃãË ixabepilone
ÃÇÁ¡Ñº capecitabine ¡Ñº capecitabine ã¹¼»Ù Ç Â·Õàè ¤Âä´ taxane áÅÐ anthracycline Áҡ͹¾ºÇÒ ixabepilone ÃÇÁ¡Ñº
capecitabine ÁÕ¡Òõͺʹͧ (43% ¡Ñº 29%; p<0.0001) áÅÐ progression-free survival (6.2 à´×͹¡Ñº 4.2 à´×͹;
p=0.0005) ·Õ´è ¡Õ ÇÒ capecitabineᵡÒÃÃÍ´ªÕÇµÔ äÁᵡµÒ§¡Ñ¹ (16.4 à´×͹ ¡Ñº 15.6 à´×͹; p=0.1162)
ÃÐÂÐàÇÅҢͧ¡ÒÃãËÂÒà¤ÁպӺѴ
㹡óշÁÕè ¡Õ ÒõͺʹͧµÍÂÒà¤ÁպӺѴ ÍÒ¨¾Ô¨ÒóÒãËÂÒà¤ÁպӺѴä»ÃÐÂÐ˹֧è (6-8 ªØ´) áÅÇËÂØ´
ËÃ×ÍãËä»àÃ×Íè Âæ ¨¹¡ÇÒâä¨ÐÅØ¡ÅÒÁµÍä»
ÃдѺ¤Óá¹Ð¹Ó 1
ÁÕ¡ÒÃÈÖ¡ÉÒà»ÃÕºà·ÕºÃÐËÇÒ§¡ÒÃãËà¤ÁպӺѴẺ intermittent ¡Ñº continuous ¾ºÇҼšÒÃÈÖ¡ÉÒ
ÂѧäÁÊÒÁÒöÂ×¹Âѹ䴪ѴਹÇÒÇÔ¸Õä˹´Õ¡Çҡѹà¾ÃÒÐÁÕ·Ñ駢ÍÁÙÅ·ÕèÇÒ ¡ÒÃãËẺ continuous äÁä´·ÓãË
ªÇ§ªÕÇµÔ Â×¹ÂÒÇ¢Ö¹é àÁ×Íè à·Õº¡Ñº intermittent(70-74) áµÍÒ¨ÁÕ progression-free survival à¾ÔÁè ÁÒ¡¢Ö¹é (70,72,73) ºÒ§ÃÒ§ҹ
¾ºÇÒ¡ÒÃãËẺ continuous ÁÕ·Ñé§ progression-free survival áÅÐ overall survival à¾ÔèÁ¢Öé¹ àÁ×èÍà·Õº¡Ñºáºº
intermittent(75,76) ÍÂÒ§äáçµÒÁ¡ÒÃãËẺ continuous ÁռŢҧà¤Õ§ÁÒ¡ÇÒẺintermittent
¢¹Ò´áÅÐÊٵâͧà¤ÁպӺѴ·Õèá¹Ð¹ÓãËãª:
CMF regimen cyclophosphamide 100 mg/m2/day po d1-14
(q 4 weeks) Methotrexate 40 mg/m2 IV d1,8
5-FU 600 mg/m2 IV d1,8
FAC regimen 5-FU 500 mg/m2 IV
(q 3 weeks) Doxorubicin 50 mg/m2 IV
Cyclophosphamdie 500 mg/m2 IV
AC regimen Doxorubicin 60 mg/m2 IV
(q 3 weeks) Cyclophosphamide 600 mg/m2 IV
FEC regimen 5-FU 500 mg/m2 IV
Epirubicin 50-90 mg/m2 IV q 3 weeks
Cyclophosphamide 500 mg/m2 IV
EC regimen Epirubicin 60-90 mg/m2 IV q 3 weeks
Cyclophosphamide 600 mg/m2 IV
Paclitaxel 175 mg/m2 IV q 3 weeks
Docetaxel 70-100 mg/m2 IV q 3 weeks
Gemcitabine 800-1250 mg/m2 IV d1,8,15 q 4 weeks (single)
1000 mg/m2 IV d1,8 q 3 weeks (combined)
Vinorelbine 25-30 mg/m2 IV d1,8 q 3 weeks
Capecitabine 1250 mg/m2 PO bid pc d1-14 q 3 weeks
(single drug)
1000 mg/m2 PO bid pc d1-14 q 3 weeks
(combined drug)
Ixabepilone 40 mg/m2 IV q 3 week
ÁÕ¡ÒÃÈÖ¡ÉÒẺ randomized controlled trial â´Â Slamon DJ et al. ã¹¼»Ù Ç Â·Õàè »¹ÁÐàÃç§àµÒ¹ÁÃÐÂÐ
á¾Ã¡ÃШÒ·ÕèÁÕ HER2 ໹¼ÅºÇ¡·ÕèäÁà¤Âä´ÃѺ¡ÒÃÃÑ¡ÉÒ´ÇÂÂÒà¤ÁպӺѴÁҡ͹ â´Âà»ÃÕºà·ÕºÃÐËÇÒ§
¡ÒÃãËÂÒà¤ÁպӺѴÍÂÒ§à´ÕÂÇ (doxorubicin ËÃ×Í epirubicin / cyclophosphamide ËÃ×Í paclitaxel) ¡Ñº¡ÒÃãË
ÂÒà¤ÁպӺѴÃÇÁ¡Ñº trastuzumab ¾ºÇÒ ¼»Ù Ç Â¡ÅÁØ ·Õäè ´ÃºÑ ÂÒà¤ÁպӺѴÃÇÁ¡Ñº trastuzumab ÁÕ굄 ÃÒ¡Òõͺʹͧ
¢Í§âä·Õ´è ¡Õ ÇÒ (50% vs 32%, p < 0.001) median time to disease progression ·ÕÂè ÒÇ¡ÇÒ (7.4 à´×͹ vs 4.6 à´×͹,
p < 0.001) áÅÐÁÕ굄 ÃÒ¡ÒÃÃÍ´ªÕÇµÔ ·ÕÁè Ò¡¡ÇÒ â´ÂÁÕ median survival 25.1 à´×͹ à·Õº¡Ñº 20.3 à´×͹ (p = 0.046)
â´ÂÁռŢҧà¤Õ§·ÕèÊÓ¤Ñ ¤×Í ¡Ò÷ӧҹ¢Í§¡ÅÒÁà¹×éÍËÑÇã¨Å´Å§ «Ö觾ºä´ÊÙ§¶Ö§ 27% 㹡ÅØÁ¼Ù»Ç·Õèä´ÃѺ
anthracycline / cyclophosphamide ÃÇÁ¡Ñº trastuzumab áÅоºä´ 13% 㹡ÅØÁ·Õèä´ÃѺ paclitaxel ÃÇÁ¡Ñº
trastuzumab ¨Ö§äÁá¹Ð¹ÓãË㪠trastuzumab ÃÇÁ¡ÑºÂÒ㹡ÅÁØ anthracycline
· ¼»Ù Ç Â·Õ¨è Ðä´ÃºÑ trastuzumab µÍ§ä´ÃºÑ ¡ÒõÃǨ¡Ò÷ӧҹ¢Í§ËÑÇ㨡͹ä´ÃºÑ ÂÒ áÅÐãªÂÒ
ä´ã¹¡Ã³Õ·ÁÕè Õ left ventricular ejection fraction ³ 50% ¼»Ù Ç Â¤ÇÃä´ÃºÑ ¡ÒõÃǨ»ÃÐàÁÔ¹¡Ò÷ӧҹ¢Í§ËÑÇ㨷ء
3 à´×͹ ã¹ÃÐËÇÒ§·Õäè ´ÃºÑ trastuzumab ÍÂÙ
ÃдѺ¤Óá¹Ð¹Ó 2A
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trastuzumab ËÅѧä´ÂҤú 1 »
· äÁá¹Ð¹ÓãË㪠trastuzumab ÃÇÁ¡ÑºÂÒà¤ÁպӺѴª¹Ô´Í×è¹ ã¹¡Ã³Õ·ÕèâäÅØ¡ÅÒÁÁÒ¡¢Öé¹ã¹
¢³Ð·Õäè ´ÃºÑ trastuzumab
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· á¹Ð¹ÓãË㪠trastuzumab 㹡ÒÃÃÑ¡ÉÒÁÐàÃç§àµÒ¹ÁÃÐÂÐá¾Ã¡ÃШÒ·ÕèÁÕ HER2/neu ໹
¼ÅºÇ¡â´Âãªà»¹ÂҪشááÃÇÁ¡ÑºÂÒà¤ÁպӺѴª¹Ô´Í×¹è ä´á¡ vinorelbine 㹡óշ¼Õè »Ù Ç Âà¤Âä´ÃºÑ adjuvant
chemotherapy ´ÇÂÂÒ¡ÅÁØ taxanes áÅÐâäÅØ¡ÅÒÁã¹ÃÐÂÐàÇÅҹ͡ÇÒ 1 »ËÅѧËÂØ´ taxanes
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ÁÕ¡ÒÃÈÖ¡ÉÒà»ÃÕºà·Õº¡ÒÃãªÂÒ trastuzumab ÃÇÁ¡ÑºÂÒ㹡ÅØÁ taxanes ¡Ñº trastuzumab ÃÇÁ¡Ñº
vinorelbine ໹ÂҪشáá㹼»Ù Ç ÂÁÐàÃç§àµÒ¹ÁÃÐÂÐá¾Ã¡ÃШÒ·ÕÁè Õ HER2 ໹¼ÅºÇ¡ äÁ¾ºÇÒÁÕ¤ÇÒÁᵡµÒ§
¡Ñ¹ã¹´Ò¹ÍѵÃÒ¡Òõͺʹͧ áÅÐ time to disease progression
· 㹡óշ¼ Õè »Ù Ç Âà¤Âä´ÃºÑ trastuzumab ໹ adjuvant treatment áÅÐÁÕ¡ÒáÅѺ໹«éӢͧâäã¹
ÃÐÂÐàÇÅÒà¡Ô¹ 1 » ÊÒÁÒö¹Ó trastuzumab ¡ÅѺÁÒãªãËÁä´
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· á¹Ð¹ÓãË㪠lapatinib 㹡ÒÃÃÑ¡ÉÒ¼Ù»ÇÂÁÐàÃç§àµÒ¹ÁÃÐÂÐá¾Ã¡ÃШÒ·ÕèÁÕ HER2/neu
໹¼ÅºÇ¡·ÕèÁÕâäÅØ¡ÅÒÁã¹¢³Ð·Õèä´ÃѺËÃ×ÍËÅѧ¨Ò¡ä´ÃѺ¡ÒÃÃÑ¡ÉÒ´Ç trastuzumab â´ÂãËãªÃÇÁ¡ÑºÂÒ
capecitabine
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References
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v v v
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83
㪪×èÍâäµÒÁẺ histopathology
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ÊàÁÕÂú¹ÊäÅ´ ¨ØÁÊäÅ´ã¹ 95%
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ethanol ·Ñ¹·Õ ËÃ×;¹´ÇÂÊà»ÃÂ
(Fine-needle aspirates) ethanol 2 ¤Ãѧé æ ÅÐ 5 ¹Ò·Õ¡Í ¹ ´Ù à Í¡ÊÒÃá¹Ç·Ò§¡ÒÃÍ Ò ¹à«ÅÅ
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(Nipple discharge sample) ÂÍÁÊÕ Papanicolaou suspicious, or negative for
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Biopsy/Core-needle biopsy ŧµÅѺ/Embed à¹×Íé ãËÍÂãÙ ¹ÃйҺ 㹡ÒÃÇÔ¹Ô¨©ÑÂËÃ×ÍäÁ/
formalin** ·Ñ¹·Õ/ÃкبӹǹªÔé¹
à´ÕÂǡѹ áÅÐàÃÕ§໹á¶ÇäÁ«Í¹ Histopathologic entity/Tumor type
ã¹ãº¢ÍµÃǨ
¡Ñ¹ and grade (if applicable)
µÃǨÊͺ¨Ó¹Ç¹ªÔé¹áÅЪÔé¹·ÕèÃкØÁÕ
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Core-needle biopsy from lesion Tumor type and grade (if
·ÕèÁÕ microcalcification/áªã¹ 10% ŧµÅѺ â´Âá¡ªÔ¹é ·ÕÃè кءºÑ ªÔ¹é Í×¹è æ/
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ÃÐºØ´Ò ¹ medial ËÃ×Í lateral,
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ÃÍÂâä (㹡óշµÕè ÃǨ¾º) ¶Ö§¢Íº type, grade/Tumor size/Lympho-
nonpalpable lesion superior ËÃ×Í inferior/¹ÓªÔ¹é à¹×Íé ä» vascular invasion status/margin
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Wide excision ·ÕèµÍ§¡Òô٠margin ¾ÃÍÁªÔ¹é à¹×Íé (¡Ã³Õ needle-guided ¡ÒÃ´Ù´Ç ÂµÒà»ÅÒ) ʧ·ÓÊäÅ´ ¢Íº¹Í¡¢Í§ÃÍÂâä¶Ö§ surgical
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Mastectomy formalin**/ ing with 1-cm thick intervals status
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µÃǨ·Ø¡ node â´Â serial 2-3 mm
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node/ËÅѧ frozen section ãÊ·Ø¡ ÃÒ§ҹ total node number áÅÐ
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Sentinel Node ªÔ¹
é ŧµÅѺᡵÒÁáµÅÐ node
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ER, PgR ãËÃÒ§ҹÃÍÂÅТͧ
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positive cells ËÃ×Í negative HER2
à¹×Íé àÂ×Íè »¡µÔÍÂãÙ ¹ºÅçÍ¡à´ÕÂǡѹ (¶Ò
¡ÒõÃǨ ER, PgR, HER2 â´ÂÇÔ¸Õ ãªºÅçÍ¡¾ÒÃÒ¿¹·ÕèÁÕà¹×éÍàÂ×èÍÁÐàÃç§ ãËÃÒ§ҹ¼Å positive, equivocal
໹ä»ä´)
Immunohistochemistry ÃÐÂÐÅØ¡ÅÒÁ ËÃ×Í negative status
ÂÍÁµÒÁ Work instruction ·Õäè ´¼Ò ¹
´ÙàÍ¡ÊÒÃËÅѡࡳ±¡ÒÃá»Å¼ÅáÅÐ
¡ÒûÃÐàÁÔ¹¤Ø³ÀÒ¾
ÃÒ§ҹ¼Å ER, PgR (˹ҷÕè 105-
106)
àÅ×Í¡ºÅçÍ¡·ÕèÁÕà¹×éÍàÂ×èÍÁÐàÃç§áÅÐÁÕ
à¹×é Í àÂ×è Í »¡µÔ Í ÂÙ ã ¹ºÅç Í ¡à´Õ Â Ç¡Ñ ¹ ãËÃÒ§ҹ¼Å positive, equivocal
¡ÒõÃǨ HER2 â´ÂÇÔ¸Õ FISH***, 㪺ÅçÍ¡¾ÒÃÒ¿¹·ÕèÁÕà¹×éÍàÂ×èÍÁÐàÃç§ áÅФÇÃàÅ×Í¡ºÅçÍ¡à´ÕÂǡѹ¡Ñº·Õè·Ó ËÃ×Í negative status
DISH*** ÅØ¡ÅÒÁ HER2 IHC (¶Ò໹ä»ä´) ÂÍÁµÒÁ ´ÙàÍ¡ÊÒÃËÅѡࡳ±¡ÒÃá»Å¼ÅáÅÐ
Work instruction ·Õèä´¼Ò¹¡Òà ÃÒ§ҹ¼Å HER2 (˹ҷÕè 108)
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* ´ÙàÍ¡ÊÒÃá¹Ç·Ò§»¯ÔºÑµÔ¡ÒÃʧµÃǨ·Ò§¾ÂÒ¸ÔÇÔ·ÂÒ
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formalin (37%-40% formaldehyde solution) 100 ml
*** FISH = Fluorescence In Situ Hybridization
DISH = Dual -color silver-enhanced in situ hybridization
54-117_pc22.pmd
87
ÃÒ¡ÒÃÊÓËÃѺµÃǨÊͺ (Check list items)
Check-list Output for CA breast
Check-list Input
(ÃÒ¡ÒÃã¹ãºÃÒ§ҹ¼Å)
· Patient identification · Type of carcinoma and grading
· Clinical information · Tumor size
· Radiological findings · Node status
· Operative procedure, location (diagram preferred) · Margins status
· Specimen handling and fixation · Lymphovascular invasion status
· Request for biomarkers (ER, PgR, HER2) · Biomarkers status (ER, PgR, HER2)
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· Microcalcification
á¹Ç·Ò§¡ÒõÃǨ¤Ñ´¡Ãͧ ÇÔ¹Ô¨©Ñ áÅÐÃÑ¡ÉÒâäÁÐàÃç§àµÒ¹Á
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2. ¡ÒûÃÐàÁÔ¹»ÃÔÁÒ³à«ÅÅ ·Õàè Ë繨ҡ¡ÓÅѧ¢ÂÒµèÓ
3. ¡ÒõÃǨà«ÅÅ·ÍÕè ÂàÙ »¹à«ÅÅà´ÕÂè Ç
4. ¡ÒõÃǨà«ÅÅ·ÍÕè ÂàÙ »¹¡ÅÁØ
5. ¡ÒõÃǨ¾×¹é ËÅѧÊàÁÕÂÃ
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1. ¤Ø³ÅѡɳÐáÅлÃÔÁÒ³¢Í§ÊÔ§è à¨Òдٴ·Õàè Ë繴ǵÒ
1.1 ºÑ¹·Ö¡ÇÒÊÔ§è à¨Òдٴ·Õäè ´ÃºÑ à»¹¹éÓ ¹éÓ»¹àÅ×Í´ ËÃ×Í à»¹ÊàÁÕÂÃ
1.2 ¡Ã³Õ໹¹éÓ ËÃ×͹éÓ»¹àÅ×Í´ ã˺ѹ·Ö¡»ÃÔÁÒµÃ໹ÁÔÅÅÔÅԵà áÅйÓä»»¹à¾×èÍ·Ó໹
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1.3 ¡ÒûÃÐàÁÔ¹»ÃÔÁÒ³¢Í§ÊàÁÕÂà ãËãªÇ´Ñ µÒÁÂÒÇ â´Âࡳ± ´Ñ§¹Õé
ÊàÁÕÂÃÁ¤Õ ÇÒÁÂÒÇ ¹Í¡ÇÒ 1 ૹµÔàÁµÃ = »ÃÔÁÒ³¹Í (small volume smear)
ÊàÁÕÂÃÁ¤Õ ÇÒÁÂÒÇ ÃÐËÇÒ§ 1-2 ૹµÔàÁµÃ = »ÃÔÁÒ³»Ò¹¡ÅÒ§ (medium volume smear)
ÊàÁÕÂÃÁ¤Õ ÇÒÁÂÒÇ ÁÒ¡¡ÇÒ 2 ૹµÔàÁµÃ = »ÃÔÁÒ³ÁÒ¡ (large volume smear)
2. ¡ÒûÃÐàÁÔ¹»ÃÔÁÒ³à«ÅÅáÅо׹é ËÅѧÊàÁÕÂà ·Õàè Ë繨ҡ¡ÓÅѧ¢ÂÒµèÓ
2.1 ËÅѡࡳ±ã¹¡ÒûÃÐàÁÔ¹»ÃÔÁÒ³à«ÅÅ ÁÕ´§Ñ ¹Õé
¨Ó¹Ç¹à«ÅÅ¹Í Â¡ÇÒ 10 µÑÇ = »ÃÔÁÒ³à«ÅÅ¹Í Â (low cellularity)
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á¡໹ÊͧÃкº ¤×Í ¡ÒÃá»Å¼Å¨Ò¡ÅѡɳÐÊàÁÕÂà (cytomorphologic base) áÅСÒÃá»Å¼ÅµÒÁâä áÅÐ
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1. ¡ÒÃá»Å¼Å¨Ò¡ÅѡɳÐÊàÁÕÂà (cytomorphologic base)
- Presence of malignant cells in clusters
- Presence of malignant cells in dispersal
- Large epithelial fragments with atypia
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Áѹè ã¨ã¹ ¼ÅÍÂ´Ù Ç Âà¾×Íè ᾷ·ÃÕè ºÑ ¼Å¨Ðãªã¹¡ÒõѴÊÔ¹ã¨ã¹¡ÒôÙáÅÃÑ¡ÉÒµÍä» Ãкº¢Í§¡ÒÃÃÒ§ҹ¼ÅÁÕ
Ẻ㪵ÑÇàŢ໹ÃËÑÊáÅÐÃкº¢Í§¡ÒÃÃÒ§ҹ¼Å·ÕèãªÇÅÕËÃ×ͤ͢ÇÒÁ ÊÓËÃѺ»ÃÐà·Èä·Â ¹ÔÂÁ㪵ÒÁ
ÃкºËÅѧ Ãкº¡ÒÃÃÒ§ҹ·Õ¹è ÓàÊ¹Í à»¹Ãкº¡ÒÃÃÒ§ҹ·Õ¼è ÊÁ¡ÒÃá»Å¼ÅµÒÁÅѡɳÐÊàÁÕÂÃáÅеÒÁ¡ÒÃ
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- Cyst with or without apocrine cells
- Scant cells, Benign change
- Inflammation
- Fibroadenomatoid feature
- Fibroadenoma
- Benign Phyllodes or cellular fibroadenoma
- Large fragment/Epithelial hyperplasia
- Atypical or suspicious cells
- Mammary carcinoma, grade specified
- Mucinous carcinoma
- Carcinoma, subtype suggested
- Lymphoma
- Spindle cell tumor/ Melanoma
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1. ÃÐÇѧ artifact
â´Â੾ÒÐÍÂÒ§ÂÔ§è forcefully smeared discohesion áÅÐ degenerating apocrine cells in cyst
2. ´Ù¡ÓÅѧ¢ÂÒµèÓ´ÇÂàÊÁÍ
㹡Òû¯ÔºµÑ §Ô Ò¹ ¤ÇÃÁÕÅӴѺ¡Ò÷ӧҹ´Ñ§¹Õé
- ´Ù»ÃÔÁÒ³´ÇµÒà»ÅÒà¾×Íè á¡ large volume, high cellularity smear ÍÍ¡¨Ò¡ small volume,
high cellularity áÅÐá¡ cyst ÍÍ¡¨Ò¡ non-cyst ໹µ¹
- ´Ù¡ÓÅѧ¢ÂÒµèÓ à¾×Íè á¡à«ÅÅà´ÕÂè Ç à«ÅÅ¡ÅÁØ áÅо׹é ËÅѧ áÅлÃÐàÁÔ¹àªÔ§»ÃÔÁÒ³
- ´Ù¡ÓÅѧ¢ÂÒÂÊÙ§ à¾×Íè ´ÙÃÒÂÅÐàÍÕ´à«ÅÅà´ÕÂÇ à«ÅÅ¡ÅÁØ áÅо׹é ËÅѧ
- ´Ù¡ÓÅѧ¢ÂÒµèÓ à¾×Íè àª×Íè Á⧡͹ÇÔ¹¨Ô ©ÑÂ
3. µÃǨÊͺ¡ÒÃÍÒ¹¡Ñº·Ò§¤ÅÔ¹¡Ô áÅÐÃѧÊÕÇ·Ô ÂÒ
¤ÇÃÁÕ¡ÒûÃЪØÁÃÇÁ·Ò§¤ÅÔ¹¡Ô ÃѧÊÕÇ·Ô ÂÒ áÅоÂÒ¸ÔÇ·Ô ÂÒ໹»ÃШÓà¾×Íè àª×Íè Áâ§à«ÅÅÇ·Ô ÂÒ
¡ÑºÅѡɳзҧ¤ÅÔ¹¡Ô ¡ÑºÃѧÊÕÇ·Ô ÂÒ ¶ÒÁÕ¤ÇÒÁ¢Ñ´á§ ¤ÇþԨÒóҷӡÒõѴªÔ¹é à¹×Íé ËÃ×͵ÃǨà¾ÔÁè àµÔÁ¡ÒõÃǨÊͺ
ÍÂàÙ ÊÁÍ·ÓãËà¡Ô´¤ÇÒÁÁѹè ã¨áÅÐÅ´¢Í¼Ô´¾ÅÒ´
¡ÒÃÍÒ¹ÁÐàÃ秷Õè໹à«ÅÅ¢¹Ò´àÅç¡ áÅÐà«ÅÅ·ÕèÁÕ differentiation ´Õ µÍ§ÍÒÈÑ»ÃÐʺ¡Òó
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References
1. The uniform approach to breast fine needle aspiration biopsy. A synopsis. Developed and approved at an NCI-sponsored conference,
Bethesda, MD, Sept. 9-10, 1996. Acta Cytol 1996; 40:1120-1126.
2. Guidelines for non-operative diagnostic procedures and reporting in breast cancer screening NHSBSP publication No.50; June 2001.
3. European guidelines for quality assurance in mammography screening, 3rd ed. 2001, p1145-1147.
4. Maygarden SJ, Novotny DB, Johnson DE, Frable WJ. Subclassification of benign breast disease by fine needle aspiration cytology. Acta
Cyto 1994;38:115-129.
v v v
¢Ñ¹
é µÍ¹¡ÒõÃǨ
1. ÈÖ¡ÉÒÃÒÂÅÐàÍÕ´áÅСÒÃÇÒ§·ÔÈ·Ò§¢Í§ªÔ¹é à¹×Íé
2. ÇÑ´¢¹Ò´¢Í§ªÔé¹à¹×éÍ·Ñ駵ÒÁá¹Ç¡ÇÒ§ (medio-lateral), á¹ÇÊÙ§ (cranio-caudal), áÅÐá¹ÇÅÖ¡
(antero-posterior) ºÑ¹·Ö¡à»¹Ë¹ÇÂૹµÔàÁµÃ
3. ÇҧἹ·ÔÈ·Ò§·Õ¨è зӡÒõѴ serial section â´Â¾Ô¨ÒóҨҡÀÒ¾àÍ¡«àÃÂáÅÐËÃ×ÍÅѡɳÐÃÍÂ
âä»ÃСͺ
4. ·ÒÊÕ (ink) à¾×Íè Ãкآͺ¢Í§´Ò¹µÒ§æ¢Í§ªÔ¹é à¹×Íé
5. µÑ´ã¹·ÔÈ·Ò§·ÕÇè ҧἹäÇ໹áǹ樹ËÁ´ ãËáµÅЪԹé ËÃ×Íáǹ (slice or section) ÁÕ¤ÇÒÁ˹Ò
»ÃÐÁÒ³ 0.5 ૹµÔàÁµÃ
6. µÃǨ´ÙÃÍÂâä ºÃÃÂÒÂÃÙ»ÅѡɳÐáÅÐÇÑ´¢¹Ò´ ºÑ¹·Ö¡ÀÒ¾ (¶Ò·Óä´)
7. ¡Ã³ÕàËç¹ÃÍÂâäªÑ´à¨¹ ãËÇ´Ñ ÃÐÂÐËÒ§¢Í§¢ÍºÃÍÂâäáÅТͺªÔ¹é à¹×Íé 4 ´Ò¹ ÊÓËÃѺªÔ¹é ·ÕÍè ÂÙ
»ÅÒ·ѧé Êͧ´Ò¹ ã˵´Ñ ã¹á¹ÇµÑ§é ©Ò¡ÍÕ¡¤Ãѧé à¾×Íè ÇÑ´ÃÐÂÐËÒ§¢Í§¢ÍºÃÍÂâäáÅТͺªÔ¹é à¹×Íé ã¹ÍÕ¡ 2 ´Ò¹
·Õàè ËÅ×Í (¡ÒÃÇÑ´¢¹Ò´ãËãªË¹ÇÂ໹ૹµÔàÁµÃ·Ñ§é ËÁ´à¾×Íè äÁÊºÑ Ê¹)
8. ¡Ã³Õ·ÃÕè ÍÂâäËÃ×͢ͺÃÍÂâääÁª´Ñ ãËÃ͵ÃǨÊͺÃÍÂâäáÅСÒÃÇÑ´ÃÐÂÐËÒ§â´Â¡Òôٷҧ
¡Åͧ¨ØÅ·ÃÃȹ
¡ÒõѴà¹×Íé ŧµÅѺ
1. µÑ´à¹×Íé ÃÍÂâä·Ñ§é ËÁ´ (¡Ã³ÕäÁà¡Ô¹ 2 ૹµÔàÁµÃ) áÅÐà¹×Íé ·Õàè »¹ fibrous breast tissueŧµÅѺ
2. ¡Ã³ÕäÁàËç¹ÃÍÂâäªÑ´à¨¹ ã˵´Ñ à¹×Íé ·Õàè »¹ fibrous breast tissue ·Ñ§é ËÁ´Å§µÅѺ
3. µÑ´ margin ·Ñ§é 6 ´Ò¹ã¹á¹Ç perpendicular ŧµÅѺ (àÅ×Í¡ºÃÔàdz·Õªè ´Ô ÁÒ¡·ÕÊè ´Ø ã¹áµÅÐ margin
¨Ó¹Ç¹ 1-2 ªÔé¹)
4. µÍ§ÃкصÓá˹§µÒ§æ¢Í§à¹×Íé ã¹·Ø¡µÅѺã˪´Ñ ਹ
v v v
B. Sections submitted
· Tumor mass(es) /Residual tumor mass(es)
- Representative sections from tumor and adjacent normal breast tissue are submitted. Addi
tional sections for ancillary study are suggested.
· Previous biopsy cavity (if present)
- Representative sections around the biopsy cavity are submitted. More sampling is indicated
in case of DCIS alone (to exclude areas of invasion).
· Deep margin and other margin(s) related to tumor
- At least one perpendicular section of the nearest deep margin and other margin(s) related to
tumor is submitted.
· Skin
- In case of suspected epidermal involvement or inflammatory breast carcinoma, represen-
tative sections from related skin are submitted.
· Nipple
- At least one section is submitted. (Cutting detail, see appendix-2)
Note: Four quadrant samplings may be helpful to detect microscopic multifocal or multicen-
tric tumor(s).
C. Microscopic examination/Diagnosis
1. Tumor mass (es)/Residual tumor(s):
· Histologic subtype: According to WHO classification or other internationally accepted classi
fication
· Grade:
· Invasive ductal carcinoma: Employ international accepted grading system (Prefer the
Modified Bloom-Richardson grade). If other grading system is used, specify the system used.
(see appendix-3 for Modified Bloom-Richardson grading system)
· Ductal carcinoma in situ: Employ the international grading system, specify the system used.
· Estimated size: Macroscopic or microscopic measurement (see appendix-4)
2. Lymphatic/vessel invasion: Blood/lymphatic vessel around tumor needs evaluation for me-
tastasis and reported if positive (see appendix-5)
3. Margin: Status of deep margin and other margin(s) related to tumor (assess the distance from
tumor to the nearest resected margin, if applicable)
4. Nipple and related skin: Status of nipple, epidermis and positive dermal blood/lymphatic vessel
invasion.
Note: 1. Histologic subtype and grading can be omitted if amount of tumor is insufficient for
evaluation.
2. There is no international recommendation for grading system of special subtype
(eg. lobular carcinoma, medullary carcinoma, mucinous carcinoma, papillary carcinoma,
etc.)
3. Tumor size around or less than 2.0 cm needed special attention. (see appendix-4)
4. In case of multifocal/multicentric tumors, all foci needed evaluation and reported.
5. Breast lesion(s) other than carcinoma should be reported.
Appendix
1. Definition of multifocal and multicentric tumor
2. Nipple cutting
3. Modified Scarff-Bloom-Richardson Grading
4. Macroscopic and microscopic measurement of mass (es)
5. Rosen criteria of lymphatic/vessel invasion
Appendix 1. Definition of multifocal and multicentric tumor
Multifocality: presence of more than a single focus of intraductal carcinoma, lobular neoplasia, or
invasive carcinoma within a slide or a biopsy specimen not larger than 5 cm in its
maximum dimension
Multicentricity: presence of independent foci of lesion (lobular neoplasia, in situ, or invasive carci-
noma) at 5 cm or more distant from one another
Appendix 2. Nipple cutting
Either approach of the following is accepted.
· Perpendicular bisection/serial section
· En face section plus perpendicular section
Appendix 3. Modified Scarff Bloom-Richardson Grading of breast carcinoma
· Tubule formation (Clear lumina must be present)
Majority of tumor (>75%) 1 point
Moderate degree (10-75%) 2 points
Little or none (<10%) 3 points
· Nuclear pleomorphism
- Uniform or regular, small nuclei and 1 point
minimal variation
- Moderate degree of variation in nuclear 2 points
size and shape, and occasional nucleoli
- Marked variation in nuclear size and bizarre 3 points
nuclei, often one or more prominent nucleoli
· Mitotic count: - Count at periphery or the most mitotically active part of the tumor, at least
10 HPF
0-5/10 HPF 1 point
6-10/10 HPF 2 points
>10/10 HPF 3 points
Note: Based on a microscopic field with a diameter of 0.44 mm and an area of 0.152 mm2
(Nikon Labophot microscope with a x40 objective lens)
Tumor grade (Tubule formation + nuclear pleomorphism + mitotic count)
3 to 5 points = Grade I, well differentiated
6 to 7 points = Grade II, moderately differentiated
8 to 9 points = Grade III, poorly differentiated
Appendix 4. Macroscopic and microscopic measurement of the mass
In case of tumor size around 2.0 cm, more accurate microscopic measurement is preferred.
Rationale :
· TNM clinical classification
T- Primary tumor
T1 = Tumor 2 cm or less in greatest dimension
T1mic = Microinvasion 0.1 cm or less in greatest dimension
T1a = More than 0.1 cm but not more than 0.5 cm in greatest dimension
T1b = More than 0.5 cm but not more than 1.0 cm in greatest dimension
T1c = More than 1.0 cm but not more than 2.0 cm in greatest dimension
T2 = Tumor more than 2 cm but not more than 5 cm in greatest dimension
T3 = Tumor more than 5 cm in greatest dimension
T4 = Tumor of any size with direct extension to chest wall or skin
References
1. Tavassoli F. General Consideration. In: Pathology of the breast. 2nded. New York: McGraw-Hill,1999: 27-74.
2. Lester SC. Breast. In. Lester SC. Manual of Surgical Pathology. 1st ed. New York: Churchill Livingstone, 2001: 129-146.
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2. Specify size of the largest metastatic deposit (macrometastases are defined as being >
0.2 cm in size, micrometastases are 0.02-0.2 cm and isolated tumor cells are less than
0.02 cm).
References
1. Tavassoli F. General Consideration. In: Pathology of the breast. 2nded. New York: McGraw-Hill,1999: 27-74.
2. Lester SC. Breast. In. Lester SC. Manual of Surgical Pathology. 1sted. New York: Churchill Livingstone, 2001: 129-146.
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»¨¨Ñ·ÕÁè ¼Õ ÅµÍ¡ÒÃÍÒ¹¼Åã˵ç¡Ñ¹
1. Preparation and staining protocol
¡Ò÷ÓãËà¹×Íé ¤§ÊÀÒ¾ (fixation) ÁÕ¤ÇÒÁÊÓ¤ÑÁҡ㹡ÒÃÃÑ¡ÉÒâ»ÃµÕ¹¢Í§à«ÅÅäÇ ¤ÇÃ᪪¹Ôé à¹×Íé
ã¹ 10% neutral buffered formalin äÁ¹Í ¡ÇÒ 6 ªÑÇè âÁ§áµäÁ¤ÇÃà¡Ô¹ 48 ªÑÇè âÁ§ à¹×Íé àÂ×Íè ªÔ¹é ãËહàµÒ¹Á·Ñ§é Íѹ
¤ÇÃầ¤ÃÖ§è ¡Í¹áªà¾×Íè ãË¡ÒëÖÁ«Òº¢Í§¿ÍÃÁÒÅԹ䴷ÇÑè ¶Ö§ªÔ¹é à¹×Íé ·Ñ§é Íѹâ´ÂàÃçÇ »ÃÔÁҵ÷Õàè ËÁÒÐÊÁ¢Í§¹éÓÂÒ
¿ÍÃÁÒÅÔ¹µÍªÔ¹é à¹×Íé ¤×ÍäÁ¹Í ¡ÇÒ 10:1
ÊÓËÃѺµÑÇÍÂÒ§à«ÅÅÇ·Ô Âҹѹé ãˤ§ÊÀÒ¾à«ÅÅ´Ç Â 95% ethanol áÅÐÂÍÁÊÕ Papanicolaou à¾×Íè
´ÙÇÒ ÁÕà«ÅÅÁÐàÃ秨ӹǹÁÒ¡¾ÍËÃ×ÍäÁ ¶ÒÁըӹǹÁÒ¡à¾Õ§¾Í ¨Ö§¤ÍÂʧÂÍÁËÒ ER áÅÐ PgR µÍä»
2. Artifacts
Artifacts à¡Ô´ä´ã¹·Ø¡¢Ñ¹é µÍ¹µÑ§é ᵡÒüҵѴ·Õãè ª¤ÇÒÁÃ͹¨¹·ÓãËà¹×Íé äËÁ ¡Òä§ÊÀÒ¾·Õäè Á
ÊÁºÙó ¡ÒÃàµÃÕÂÁºÅçÍ¡áÅСÒõѴà¹×Íé àÂ×Íè ໹ἹºÒ§ µÅÍ´¨¹¶Ö§¡ÒÃÂÍÁ »ËҢͧ artifacts ¤×Í·ÓãË¡ÒÃ
µÔ´ÊÕ¼´Ô à¾ÕÂé ¹ä»
References
1. Harris L, Fritsche H, Mennel R, et al: American Society of Clinical Oncology 2007 Update of Recommendations for the Use of Tumor
Markers in Breast Cancer. J Clin Oncol 2007; 25:1-26.
2. Allred DC, Brown P, Medina D. The origins of estrogen receptor alpha-positive and estrogen receptor slpha-negative human breast
cancer. Breast Cancer Res 2004; 6: 240-245.
3. Dabbs DJ. Breast Pathology. Philadelphia: Elsevier Saunders; 2012.
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¼ÅºÇ¡ (Positive HER2 status) àÁ×Íè ¹Ñº¨Ó¹Ç¹ dot ä´¤Ò > 5 dots / nucleus «Ö§è ầ໹
- Low amplification: àÁ×è͹Ѻ¨Ó¹Ç¹ dot ä´¤ÒÃÐËÇÒ§ 6-10 dots µÍ nucleus ËÃ×;º small
clusters ËÃ×Í໹ mixture of multiple dots áÅÐ small clusters of the HER2 gene present per
nucleus in > 50% of cancer cell
- High amplification: àÁ×è͹Ѻ¨Ó¹Ç¹ dot ä´ÁÒ¡¡ÇÒ 10 dots (>10) µÍ nucleus ËÃ×;º large
clusters ËÃ×Í໹ mixture of multiple dots áÅÐ large clusters of the HER2 gene present per
nucleus in > 50% of cancer cell
¼Åź (Negative HER2 status) àÁ×Íè ¹Ñº¨Ó¹Ç¹ dot ä´µ§Ñé áµ 5 ŧÁÒ (£ 5)
Diploid: àÁ×Íè ¹Ñº¨Ó¹Ç¹ dot ä´1-2 dots of the HER2 gene µÍ nucleus in > 50% of cancer
cell
Polysomy: àÁ×Íè ¹Ñº¨Ó¹Ç¹ dots ä´ 3-5 dots of the HER2 gene µÍ nucleus in > 50% of cancer
cell
¡ÒùѺ signal - a single dot (signal) ÁÕÅѡɳÐ໹¨Ø´¡ÅÁ¢ÍºàÃÕº¾ºä´ã¹ nucleus ¢Í§
normal cell ã¹ slide à´ÕÂǡѹ (use as reference)
- a small cluster ÁÕÅ¡Ñ É³Ð໹¡ÅÁØ ¢Í§ dot ·Õ¢è ͺäÁàÃÕº ¢¹Ò´ 3-5 à·Ò¢Í§ single
dot
- a large cluster ÁÕÅ¡Ñ É³Ð໹¡ÅÁØ ¢Í§ dot ·Õ¢è ͺäÁàÃÕº ¢¹Ò´ãË¡ÇÒ 5 à·Ò¢Í§
single dot
· ¡ÒÃá»Å¼Å HER2 â´Âà·¤¹Ô¤ Dual-color silver-enhanced in situ hybridization (HER2
DISH)(3, 6, 7)
ÇÔ¸¡Õ ÒÃá»Å¼ÅãªÇ¸Ô ¡Õ ÒùѺ¨Ó¹Ç¹ dot (signal) ¢Í§ HER2 «Ö§è µÔ´ÊմӢͧ silver áÅÐ Chromo-
some 17 (Chr 17) «Ö觵ԴÊÕᴧ㹠nucleus ¢Í§ tumor cell 㹺ÃÔàdz invasive breast cancer ·ÕèᵡµÒ§¡Ñ¹ 2
µÓá˹§ ¹Ñºá˧ÅÐ 20 nuclei áÅФӹdzËÒÍѵÃÒÊǹÃÐËÇÒ§ total number of HER2 signals in 40 nuclei µÍ
total number of Chr17 signals in 40 nuclei, (HER2/Chr17 ratio) áÅÇÃÒ§ҹ¼Å´Ñ§¹Õé
¼ÅºÇ¡: Amplification of HER2 gene using HER2 DISH method.
(HER2/Chr 17 ratio is 2)
¼Åź: No amplification of HER2 gene using HER2 DISH method.
(HER2/Chr17 ratio is 2)
¡ÒùѺ signal - ÁÕ·§Ñé single dot (copy, or signal), multiple dots, small cluster áÅÐ large cluster
- ¢¹Ò´¢Í§áµÅÐ dot ÍÒ¨ vary ä´ã¹áµÅÐ case ãË㪢¹Ò´¢Í§ dot ã¹ HER2
ËÃ×Í Chr 17 ã¹ nucleus ·Õè໹ non-neoplastic cells હ stromal fibroblasts,
endothelial cells, lymphocytes áÅÐ benign breast epithelial cells ໹ internal
positive control ¢Í§ slide ¹Ñ¹é æ (ãªà»¹ reference) 㹡ÅÁØ ¹Õ¨é оº normal HER2
or Chr17 signals ·ÕÁè Õ 1-2 copies µÍ nucleus
- a small cluster ÁÕ¢¹Ò´à·Ò¡Ñº 6 dots
- a large cluster ÁÕ¢¹Ò´à·Ò¡Ñº 12 dots
References
1. Sampatanukul P, Chaiwun B, Wongwaisayawan S, Suwanagool P, Vinyuvat S, Karalak A, Praditphol N, Paueksakon P, Ruangvejvorachai
P, Field AS, Wannakrairot P. A two-phase study model for the standardization of HER2 immunohistochemical assay on invasive ductal
carcinoma of the breast. J Med Assoc Thai 2005; 88:1680-1688.
2 Wang S, Saboorian M, Frenkel EP, Haley BB, Siddiqui MT, Gakaslan S, et al. Aneusomy 17 in breast cancer: its role in HER-2/neu
protein expression and implication for clinical assessment of HER-2/neu status. Mod Pathol 2002; 15:137-145.
3 Wolff AC, Hammond MEH, Schwartz, Hagerty KL, Allred DC, Cote RJ, et al. American Society of Clinical Oncology/College of
American Pathologists Guideline Recommendations for human epidermal growth factor receptor 2 testing in breast cancer. J Clin Oncol
2007; 25:118-145.
4. Tanner M, Gancberg D, Leo AD, Larsimont D, Rouas G, Piccart MJ, et al. Chromogenic in situ hybridization (CISH): a pratical
alternative for FISH to detect HER-2/NEU oncogene amplification in archival breast cancer samples. Am J Pathol 2000; 157:1467-72.
5. Di Palma S, Collins N, Bilous M, Sapino A, Mottolese M, Kapranos N, et al. A quality assurance exercise to evaluate the accuracy
and reproducibility of chromogenic in situ hybridization for HER2 analysis in breast cancer. J Clin Pathol 2008; 61:757-60.
6. Dietel M, Ellis IO, H?fler H, Kreipe H, Moch H, Dankof A, et al. Comparison of automated silver enhanced in situ hybridization (SISH)
and fluorescence ISH (FISH) for the validation of HER2 gene status in breast carcinoma according to the guidelines of the American
Society of Clinical Oncology and the College of American Pathologists. Virchows Arch 2007; 451:19-25.
7. Kang J, Kwon GY, Lee YH, Gong G. Comparison of silver-enhanced in situ hybridization and fluorescence in situ hybridization for
HER2 gene status in breast carcinomas. J Breast Cancer 2009; 12:235-40.
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¡ÒÃá»Å¼Å Ki-67
¡ÒÃá»Å¼Åãªà¡³±´§Ñ ¹Õé
¼ÅºÇ¡ (Positive test) ¤×Íà«ÅÅÁÐàÃç§ã¹Êǹ¢Í§ invasive carcinoma ÁÕ¡ÒõԴÊÕ·Õè nucleus
¼Åź (Negative test) ¤×ÍäÁ¾º nucleus ¢Í§à«ÅÅÁÐàÃ秵ԴÊÕ
ËÁÒÂà˵Ø
1. ¡ÒÃÂÍÁÊÕ·àÕè ËÁÒÐÊÁà«ÅÅ»¡µÔહ à«ÅÅ·ÁÕè ¡Õ ÒÃầµÑǤÇÃÁÕ¡ÒõԴÊÕ·Õè nucleus
2. ¶ÒªÔé¹à¹×éÍÁÕ¡ÒõԴÊÕ·ÕèÊÁèÓàÊÁÍ á¹Ð¹Óã˹ѺÍÂÒ§¹Í 3 ºÃÔàdz´Ç high power (x40
objective) à¾×Íè ãËä´à«ÅÅÁÐàÃç§ÍÂÒ§¹Í 500-1000 à«ÅÅ(4)
3. ¶ÒªÔ¹é à¹×Íé ÁÕ¡ÒõԴÊÕäÁÊÁèÓàÊÁÍ ÂѧäÁÁ¢Õ Í ÊÃØ»·Õªè ´Ñ ਹÇҨйѺ¨Ò¡ºÃÔàdzã´(4)
¡ÒÃÃÒ§ҹ¼Å Ki-67
ãËÃÒ§ҹ¼ÅÇÒ positive ËÃ×Í negative ¾ÃÍÁÃÐºØ¤Ò »ÃÐàÁÔ¹ÃÍÂÅТͧà«ÅÅÁÐàÃ秷Õãè ˼źǡ
References
1. Harris L, Fritsche H, Mennel R, et al. American Society of Clinical Oncology 2007 update of recommendations for the use of tumor
markers in breast cancer. J Clin Oncol 2007;25(33)5287-5312.
2. Goldhirsch A, Wood WC, Coates AS et al. Strategies for subtypes-dealing with the diversity of breast cancer: highlights of the St Gallen
International Expert Consensus on the Primary Therapy of Early Breast Cancer 2011. Ann Oncol 2011;22(8)1736-1747.
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