Cancer - 2000 - Ernst - The Prevalence of Complementary Alternative Medicine in Cancer

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777

The Prevalence of Complementary/Alternative


Medicine in Cancer
A Systematic Review

Edzard Ernst, M.D., Ph.D. BACKGROUND. Complementary/alternative cancer treatments are believed to be
Barrie R. Cassileth, Ph.D.2 prevalent. However, reliable prevalence rates do not exist. The aim of this review
was to summarize the existing data on this topic.
1
Department of Complementary Medicine, Post- METHODS. A series of computerized literature searches was performed to locate all
graduate Medical School, University of Exeter, Ex- published studies documenting the prevalence of complementary and/or alterna-
eter, United Kingdom. tive therapy (CAM) use among patients with cancer.
2
Department of Medicine (Oncology), University of RESULTS. A total of 26 surveys from 13 countries, including 4 studies of pediatric
North Carolina, Chapel Hill, North Carolina. patients, was retrieved. The use of CAM therapies in adult populations ranged from
7– 64%. The average prevalence across all adult studies was 31.4%.
CONCLUSIONS. This large degree of variability most likely is due to different un-
derstandings of “complementary/alternative medicine” on the part of both inves-
tigators and patients. It is likely that the results of the current study reflect the
primarily adjunctive use of CAM treatments. Future studies should use a standard-
ized protocol to determine the true prevalence of these therapies more closely.
Cancer 1998;83:777– 82. © 1998 American Cancer Society.

KEYWORDS: alternative medicine, complementary therapies, cancer, prevalence,


adjunctive therapy.

C omplementary/alternative medicine (CAM) is used by 25%-50% of


the general population of industrialized nations.1–3 It has been
described as “diagnosis, treatment and/or prevention which comple-
ments mainstream medicine by contributing to a common whole, by
satisfying a demand not met by orthodoxy or by diversifying the
conceptual frameworks of medicine,”4 a definition recently adopted
by the Cochrane Field in Complementary Medicine. Some “alterna-
tive” therapies are promoted not to complement mainstream medi-
cine, but to substitute for it. These products and regimens, unproved
and deemed unpromising by oncologists, typically are invasive and
costly.
The reasons for CAM’s present popularity most certainly are
complex.5 They are related to the social and cultural context.6 In cases
of severe illness, the hope to “leave no stone unturned” is a powerful
motivator.5 This renders cancer patients prime candidates for CAM
Address for reprints: Edzard Ernst, M.D., Ph.D., use.6,7 There is evidence to suggest that oncologists, although often
Department of Complementary Medicine, Post- unfamiliar with CAM, may take a less negative view of CAM use today
graduate Medical School, University of Exeter, 25
than they did previously.8
Victoria Park Road, Exeter EX2 4NT, UK.
This systematic review attempted to summarize the published
Received December 5, 1997; revision received data on CAM use in oncology. Secondary aims were to detect national
February 10, 1998; accepted February 19, 1998. differences and trends when possible.

© 1998 American Cancer Society


10970142, 1998, 4, Downloaded from https://acsjournals.onlinelibrary.wiley.com/doi/10.1002/(SICI)1097-0142(19980815)83:4<777::AID-CNCR22>3.0.CO;2-O, Wiley Online Library on [31/10/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
778 CANCER August 15, 1998 / Volume 83 / Number 4

TABLE 1
Key Data from All Investigations Included

Authors (year of
publication) Sample (country) Method type of treatments Prevalence Comment

Faw et al.9 (1977) 69 pediatric cancer Interview and Laetrile, folk remedies, healing 9% had tried some 25% had received
patients or parents questionnaire form of CAM recommendations to try CAM
(U.S.)
Arkko et al.10 (1980) 151 consecutive Personal interviews Herbs, vitamins, diet 56% of female and 30% 38% of users had confidence in
outpatients with of male patients had CAM
cancer (Finland) used CAM
Pendergras et al.11 (1981) Families of 106 pediatric Interviews Knowledge/use of laetrile and 16% of children had Accuracy of toxic effects poor
cancer patients (U.S.) seven other alternatives used CAM
determined
Fereberger et al.12 (1983) 183 outpatients with Questionnaire Mainly herbal remedies 59% had tried some Survey only published an abstract
various cancers form of CAM
(Austria)
Cassileth et al.13 (1984) 304 inpatients with Personal interviews Metabolic treatments, diets, 54% of patients 40% of patients had abandoned
cancer and 356 megavitamins, imagery, receiving conventional therapy for CAM.
patients of CAM spiritual healing, immune conventional Costs were often considerable
practitioners (U.S.) stimulants therapy used CAM
in addition
Eidinger et al.14 (1984) 315 patients with Interview Laetrile, vitamins diets 7% had tried some 70% would try CAM if available
metastatic tumors form of CAM
(U.S.)
Obrist et al.15 (1986) 101 consecutive patients Interview Beetroot juice, vitamins, 32% had used or were More men than women used;
with cancer Iscador, herbs, lactic acid, using CAM Iscador known by physicians;
(Germany) homeopathic medications other methods known in only
25% of cases
Clinical Oncology Group16 463 outpatients with Personal interview Diets, vitamins, herbs, laetrile 37% had sought advice Compliance with CAM advice was
(1987) cancer (New Zealand) regarding CAM only 19%, costs for CAM often
were high
Beaufort et al.17 (1988) 295 put-patients with Questionnaire Herbs, diets vitamins 51% had used CAM CAM mostly used in addition to
gynecologic cancers since diagnosis conventional treatments and
(Austria) mostly judged as effective (by
patients)
Berger et al.18 (1989) 494 outpatients Questionnaire (33% Diet, anthroposophic 71 patients were using main reason (in 87%): to build up
(Switzerland) response rate) rememdies, vitamins CAM resistance
‘‘detoxification’’
Morant et al.19 (1991) 300 consecutive cancer Questionnaire (53% Herbs, healing homoeopathy 52% had used CAM Younger patients were more likely
outpatients response rate) diets to use CAM. Most frequent
(Switzerland) reason was to do everything
possible to regain health
Lerner et al.20 (1992) 2743 cancer patients Telephone Not specified 9% had used at least 1 In 73% of the cases CAM use
(representative of all interview type of CAM in their recommended by physician. 6%
cancer patients) (U.S.) lifetime experienced adverse effects of
CAM, costs often were high
Burke and Sikora21 (1993) 100 new consecutive Structured personal Counseling, meditation, 32% had used some 66% would have accepted CAM if
patients with various interview relaxation, visualization, form of CAM offered by the hospital
cancers (U.K.) healing
Damkier et al.22 (1994) 769 outpatients with Questionnaire (97% Coenzyme Q10 45% used CAM CAM use in women more frequent
cancer (Denmark) response rate) than in men
Downer et al.23 (1994) 600 unselected oncology Postal Healing, relaxation, 16% had used CAM 82% of patients were (very)
patients (U.K.) questionnaire visualization, diets, satisfied with CAM; adverse
and personal homoeopathy effects of diets were reported
interview (n 5
48)
Sawyer et al.24 (1994) 48 children with cancer Questionnaire filled Imagery, hypnotherapy, 46% had used at least 1 Less than 50% of parents had
(Australia) in by parent relaxation, diets, type of CAM since discussed CAM use with
multivitamins diagnosis physician
(continued)
10970142, 1998, 4, Downloaded from https://acsjournals.onlinelibrary.wiley.com/doi/10.1002/(SICI)1097-0142(19980815)83:4<777::AID-CNCR22>3.0.CO;2-O, Wiley Online Library on [31/10/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
Alternative Medicine and Cancer/Ernst and Cassileth 779

TABLE 1 (continued)

Authors (year of
publication) Sample (country) Method type of treatments Prevalence Comment

van der Zouwe et al.25 949 patients with various Face to face ‘‘Alternative treatments’’ 9.4% were current users Young, highly educated patients in
(1994) forms of cancer from interview and (not specified) palliative care were likely users;
several outpatient questionnaire the majority hoped alternative
departments (Holland) therapies would slow disease
progression
Risberg et al.26 (1995) 642 patients with various Questionnaire Healing, homoeopathy, 20% were current users, 40% of users had used alternative
cancers from various reflexology, herbs, vitamins, healing was the most treatments prior to their cancer
centers (Norway) diets, Nitter therapy, Iscador prevalent (12%) diagnosis
and other (not specified)
therapies
Risberg et al.27 (1995) 252 patients with various Questionnaire Healing, homoeopathy, herbs, 20% used at least one Patients without cancer held a more
forms of cancer from diets, reflexology, Nitter treatment, 2% used positive view on the benefits of
inpatient and therapy (specifically named), combinations, healing alternative treatments than
outpatient departments plus any other alternative was the most cancer patients
(Norway) therapy the patient listed prevalent (9.0%)
Begbie et al.28 (1996) 507 outpatients with Questionnaire (66% Diets, psychologic methods 22% had used CAM Average annual cost of $530 was
cancer (Australia) response rate) perceived as value for money.
40% did not discuss CAM use
with their physician
Jirillo et al.29 (1996) 563 questionnaires Anonymous surveys Any unconventional cancer 17% of respondents in Results were similar in Italy and
distributed to cancer treatment each country used Argentina. 20–38% of alternative
patients in Italy; 400 in alternative methods treatments were proposed by
Argentina physicians
Liu et al.30 (1997) 100 consecutive patients Questionnaire Chinese medication 64% took such Prevalence higher in females, many
with advanced cancer medications hoped for a miracle cure;
(Taiwan) information on CAM rarely came
from physicians, costs normally
were moderate
Möttönen and Uhari31 15 children with acute Patient diaries ‘‘alternative medicines’’ (not 40% of the patients used The investigation included a age-
(1997) lymphoblastic specified) alternative treatments matched, noncancer control
leukemia from one group, 8% of whom used
pediatric department alternative treatments
(Finland)
Sollner et al.32 (1997) 215 patients with Questionnaire Any unconventional cancer 14% of patients used Alternative therapies used in
melanoma (Austria) therapy alternative therapies supplementary fashion
Rasky (unpublished data) 154 patients attending an Questionnaire 74 different unconventional 62% had used CAM, 33% Young patients and married
(1997) oncology clinic methods mistletoe, 20% Bach patients used CAM more
(Austria) flower, remedies, 20% frequently
homoeopathy
Risberg et al.33 (1998) 252 patients (as in initial Questionnaire with Healing, homoeopathy, Prevalence increased In only follow-up study to date, 5-
survey). Reduction in follow-ups after reflexology, herbs, vitamins, during follow-up: 26% year survival was notinfluenced
sample size over time 4, 12, 24, and 60 diets, injection therapies at 4 months, 24% at by CAM use
(110 after 60 months) months and (e.g., Nitter, Iscador), plus 12 months, 18% at 24
(Norway) telephone any other alternative therapy months, and 27% at
interview after the patient listed 60 months; women
last question- used CAM more
naire frequently than men

CAM: complementary/alternative medicine.

METHODS scanned for further relevant contributions. Inclusion


The following databases were searched from their in- in this review required original data relating to the
ception through January 1998 for articles on cancer prevalence of CAM in samples of patients with cancer.
and CAM: MEDLINE, Embase, and CISCOM (a data- There were no restrictions regarding the language of
base specializing in the “grey” literature of CAM). The the articles. All articles were read in full and data were
authors’ own extensive files also were consulted. The extracted in a standardized, predefined fashion (Table
bibliographies of all articles thus retrieved were 1). We have not reviewed the original data behind the
10970142, 1998, 4, Downloaded from https://acsjournals.onlinelibrary.wiley.com/doi/10.1002/(SICI)1097-0142(19980815)83:4<777::AID-CNCR22>3.0.CO;2-O, Wiley Online Library on [31/10/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
780 CANCER August 15, 1998 / Volume 83 / Number 4

studies listed here. We have in all cases accepted the veys published in 199730-32 and by Rasky et al. (un-
original authors’ representations as true and evi- published data) yield prevalence rates ranging from
dence-based. 14%-64%. Two of these surveys are from the same
country (reference 32 and Rasky et al.), but suggest
RESULTS vastly different prevalence rates.
Twenty-six publications were found (references 9 –33 The lack of specificity and inconsistent definitions
and Rasky et al., unpublished data), including 1 fol- of CAM contribute significantly to this variability.
low-up report of previously studied patients. The key CAM often is not defined in prevalence studies or is
data from these reports are summarized in Table 1. defined so broadly as to include all treatments re-
Increasing interest in CAM use among patients with ceived outside of a hospital. Thus the inclusion of
cancer is reflected in the geometric growth in the counseling, group therapy, and other activities more
numbers of publications on the subject. A single arti- appropriately counted as mainstream, as well as well-
cle was published in the 1970s, 9 in the 1980s, and 16 ness regimens, self-help efforts, home remedies, and
between 1990 to date. other non-CAM activities in respondents’ answers dis-
Publications were based on studies conducted in tort the actual extent of CAM utilization.
13 countries. The majority of articles came from the Although some studies uncovered for this analysis
U. S. (five articles) and Germany (four). Investigators indicate that patients used CAM in an adjunctive or
in South America, Australia, New Zealand, and China supplementary fashion, prevalence studies rarely dif-
also conducted studies, as did researchers in many ferentiate between therapies used in an adjunctive
Western European countries. mode and those applied toward “cure,” exclusive of
The 4 articles concerning pediatric patients (from mainstream treatment. With one exception,13 the
Australia, Finland, and the U. S. [2 publications]), sug- studies reported here include patients seen in main-
gest but do not show conclusively a growth in the use stream cancer programs only. Therefore, by definition
of alternative therapies in children from 9% in 1977 to patients who were receiving cancer care in other set-
16% in 1981, 46% in 1994, and 40% in 1997. Data from tings and who may have been receiving alternatives to
these four studies cannot prove actual growth because mainstream care were not represented in these inves-
the studies are not consistent in their definitions or tigations.
methodology. Laetrile (l-mandelonitrile-b-glucuronic Most surveys also are open to biases. For example,
acid), common in the earliest pediatric studies, was selection bias can result from the choice of study
replaced in later years by CAM therapies of greater sample, and high nonresponse rates and recall bias
contemporary interest, such as imagery, hypnother- may occur in retrospective analyses. Moreover, it
apy, relaxation, diets, and multivitamins. should be noted that physicians’ comments as re-
Of the 21 studies involving adult cancer patients, ported by patients may be inaccurate. Discrepancies
50% reported that up to 27% of respondents used between what the patient heard or remembered and
CAM; the remaining studies found that . 25% of re- what the physician actually said may well exist.
spondents tried CAM therapies. Percentages range As CAM has become more widely discussed by the
from a low of 7% to a high of 64%. The average per- media and in mainstream medicine, patients are likely
centage use across adult studies was 31.4%. to feel more comfortable about reporting their use of
Although the particular nature of CAM is not al- these therapies. Thus, the apparently increased rates
ways specified, reported regimens range widely from seen today also may reflect patients’ willingness to talk
diets and relaxation to iscador and Chinese medica- more openly about their use of CAM.
tions. In the 1990s, the most commonly noted CAM Data from pediatric surveys reviewed here
therapies across all studies include mind-body ap- suggest an increase in CAM use or reports of use
proaches (meditation, relaxation, hypnotherapy, visu- during the last 20 years. Although longitudinal data
alization, and other imagery techniques), reflexology, by Risberg et al. might suggest such an increase in
dietary approaches and food supplements, Chinese adults as well, these same data also could reflect
medications, botanical preparations, homeopathy, increased use of CAM by the same patients as their
and spiritual healing. disease advances,33 or more open reporting by pa-
tients.
DISCUSSION Regardless, it is clear that patients with cancer in
The studies reported in this article display an appar- Europe, Asia, the Americas, and Australia use CAM
ently wide range of prevalence for CAM use. This is frequently. Although Chinese medications are sought
not explained by either regional variations or increas- most commonly in Asia, as would be expected, re-
ing popularity over time. For example, the three sur- maining CAM approaches differ little from country to
10970142, 1998, 4, Downloaded from https://acsjournals.onlinelibrary.wiley.com/doi/10.1002/(SICI)1097-0142(19980815)83:4<777::AID-CNCR22>3.0.CO;2-O, Wiley Online Library on [31/10/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
Alternative Medicine and Cancer/Ernst and Cassileth 781

country. Given this degree of consistency as well as lmittel und Paramedizin in der Onkologie - Ergebnisse einer
popularity, physicians’ lack of knowledge about CAM Umfrage. Wien Med Wochenschr 1983;17:443.
13. Cassileth BR, Lusk EJ, Strouse TB, Bodenheimer BJ. Contem-
requires careful consideration.34
porary unorthodox treatments in cancer medicine. Ann In-
Critical analyses of this area should inform both
tern Med 1984;101:105–2.
the patient and the physician.35,36 In particular, future 14. Eidinger RN, Schapira DV. Cancer patients’ insight into their
research should clarify distinctions between poten- treatment, prognosis, and unconventional therapies. Cancer
tially harmful alternative “cancer cures” and poten- 1984;53:2736 – 40.
tially beneficial complementary therapies employed 15. Obrist R, von Meiss M, Obrecht JP. The use of paramedical
as adjuncts to cancer treatment.7 treatment methods by cancer patients. A inquiry on 101
ambulatory patients [in German]. Dtsch Med Wochenschr
Future studies might seek to apply a more stan-
1986;111:283–7.
dard series of questions and definitions to generate 16. Clinical Oncology Group. New Zealand cancer patients and
comparable data. A better understanding then could alternative medicine. N Z Med J 1987;100:110 –3.
be reached regarding patients’ expectations, reactions, 17. Beaufort F, Drofenik M, Pleyer K. Beurteilung von Medika-
costs, discussion of CAM with their physicians, clinical menten mit fraglicher Wirksamkeit und sogenannten
outcomes, and optimal uses of complementary thera- Naturheilmittels in der Onkologie durch den Patienten.
pies in future cancer care. Although CAM use has been Wien Med Wochenschr 1988;4:85–91.
18. Berger DP, Obrist R, Obrecht JP. Tumorpatient und Para-
found in surveys of cancer patients around the world,
medizin. Dtsch Med Wochenschr 1989;114:323–30.
its impact on cancer patients’ well-being has been 19. Morant R, Jungi WF, Koehli C, Senn HJ. Warum benützen
explored only minimally.37 Tumorpatienten Alternativmedizin? Schweiz Med Wochen-
Despite the absence of reliable prevalence figures, schr 1991;121:1029 –34.
we conclude that the use of CAM by cancer patients is 20. Lerner IJ, Kennedy BJ. The prevalence of questionable
common and widespread. Consistently defined infor- methods of cancer treatments in the United States. CA Can-
mation and data on alternative versus complementary cer J Clin 1992;42:181–91.
21. Burke C, Sikora K. Complementary and conventional cancer
use of unconventional regimens are needed to inform
care: the integration of two cultures. Clin Oncol (R Coll
the debate regarding the potential benefits or harms of Radiol) 1993;5:220 –7.
such treatments. 22. Damkier A, Bonce Jensen A, Rose C. Kræftpatienters brug af
Q10. Ugeskr Laeger 1994;156:813– 8.
REFERENCES 23. Downer SM, Cody MM, McCluskey P, Wilson PD, Arnott SJ,
1. Eisenberg DM, Kessler RC, Foster C, Norlock FE, Calkins DR, Lister TA, et al. Pursuit and practice of complementary
Delbanco TL. Unconventional medicine in the United therapies by cancer patients receiving conventional treat-
States. N Engl J Med 1993;328:246 –52. ment. BMJ 1994;309:86 –9.
2. Fisher P, Ward A. Complementary medicine in Europe. BMJ 24. Sawyer MG, Gannoni AF, Toogood IR, Antoniou G, Rice M.
1994;309:107–11. The use of alternative therapies by children with cancer.
3. MacLennan AH, Wilson DH, Taylor AW. Prevalence and cost Med J Aust 1994;160:320 –2.
of alternative medicine in Australia. Lancet 1996;347:569 –73. 25. van der Zouwe N, van Dam FS, Aaronson NK, Hanewald GJ.
4. Ernst E, Resch KL, Mills S, Hill R, Mitchell A, Willoughby M, Alternative treatments in cancer: extent and background of
et al. Complementary medicine - a definition. Br J Gen Pract utilisation. Ned Tijdschr Geneeskd 1994;138:300 – 6.
1995;45:506. 26. Risberg T, Lund E, Wist E. Use of non-proven therapies.
5. Ernst E, Willoughby M, Weihmayr TH. Nine possible reasons Differences in attitudes between Norwegian patients with
for choosing complementary medicine. Perfusion 1995;11: non-malignant disease and patients suffering from cancer.
356 – 8. Acta Oncol 1995;34:893– 8.
6. Cassileth BR, Chapman CC. Alternative and complementary 27. Risberg T, Lund E, Wist E, Dahl O, Sundstrøm S, Andersen
cancer therapies. Cancer 1996;77:1026 –34. OK, et al. The use of non-proven therapy among patients
7. Ernst E. Complementary cancer treatments: hope or hazard? treated in Norwegian Oncological departments. A cross-
Clin Oncol (R Coll Radiol) 1995;7:259 –3.
sectional national multicentre study. Eur J Cancer 1995;31A:
8. Bourgeault IL. Physicians’ attitudes toward patients’ use of
1785–9.
alternative cancer therapies. Can Med Assoc J 1996;15:1679 –
28. Begbie SD, Kerestes ZL, Bell DR. Patterns of alternative
85.
medicine use by cancer patients. Med J Aust 1996;165:545– 8.
9. Faw C, Ballentine R, Ballentine L, vanEys J. Unproved cancer
remedies. A survey of use in pediatric outpatients. JAMA 29. Jirillo A, Lacava J, Leone BA, Lonardi F, Bonciarelli G. Survey
1977;238:1536 – 8. on the use of questionable methods of cancer treatment.
10. Arkko PJ, Arkko BL, Kari-Koskinen O, Taskinen PJ. A survey GOCS. Grupo Oncologico Cooperativo del Sur Republica
of unproven cancer remedies and their users in an outpa- Argentina. Tumori 1996;82:215–7.
tient clinic for cancer therapy in Finland. Soc Sci Med 1980; 30. Liu JM, Chu HC, Chin YH, et al. Cross sectional study of use
14A:511– 4. of alternative medicines in Chinese cancer patients. Jpn
11. Pendergrass TW, Davis S. Knowledge and use of “alterna- J Clin Oncol 1997;27:37– 41.
tive” cancer therapies in children. Am J Pediatr Hematol 31. Möttönen M, Uhari M. Use of micronutrients and alterna-
Oncol 1981;3:339 – 45. tive drugs by children with acute lymphoblastic leukemia.
12. Fereberger W, Samonigg H, Pfeiffer KP, Rainer F. Naturhei- Med Pediatr Oncol 1997;28:205– 8.
10970142, 1998, 4, Downloaded from https://acsjournals.onlinelibrary.wiley.com/doi/10.1002/(SICI)1097-0142(19980815)83:4<777::AID-CNCR22>3.0.CO;2-O, Wiley Online Library on [31/10/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
782 CANCER August 15, 1998 / Volume 83 / Number 4

32. Sollner W, Zingg-Schir M, Rumpold G, Fritsch P. Attitude 35. Montbriand MJ. An overview of alternate therapies
toward alternative therapy, compliance with standard treat- chosen by patients with cancer. Oncol Nurs 1994;21:1547–
ment, and need for emotional support in patients with 54.
melanoma. Arch Dermatol 1997;133:31–321. 36. Cassileth BR. The alternative medicine handbook: the com-
33. Risberg T, Lund E, Wist E, Kaasa S, Wilsgaard T. Cancer plete reference guide to alternative and complementary
patients use of nonproven therapy. A 5-year follow-up therapies. New York: WW Norton, Inc., 1998.
study. J Clin Oncol 1998;16:6 –12. 37. Cassileth BR, Lusk EJ, Guerry D, Blake AD, Walsh WP, Kas-
34. Crocetti E, Crotti N, Montella M, Musso M. Complementary cius L, et al. Survival and quality of life among patients on
medicine and oncologists’ attitudes. A survey in Italy. Tu- unproven versus conventional cancer therapy. N Engl J Med
mori 1996;82:539 – 42. 1991;324:1180 –5.

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