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DICOM RT Mode Reference Guide
DICOM RT Mode Reference Guide
DICOM RT Mode Reference Guide
Reference Guide
Notice Information in this user guide is subject to change without notice and does not
represent a commitment on the part of Varian. Varian is not liable for errors
contained in this user guide or for incidental or consequential damages in
connection with furnishing or use of this material.
This document contains proprietary information protected by copyright. No part
of this document may be reproduced, translated, or transmitted without the
express written permission of Varian Medical Systems, Inc.
FDA 21 CFR 820 Varian Medical Systems, Oncology Systems products are designed and
Quality System manufactured in accordance with the requirements specified within this federal
Regulations regulation.
(CGMPs)
ISO 13485 Varian Medical Systems, Oncology Systems products are designed and
manufactured in accordance with the requirements specified within the ISO
13485 quality standard.
EU REACH SVHC The link to the current EU REACH SVHC disclosure statement can be found at
Disclosure http://www.varian.com/us/corporate/legal/reach.html
CAUTION: US Federal law restricts this device to sale by or on the order of a physician.
Trademarks ARIA® oncology information system, Clinac® iX linear accelerator, On-Board Imager® kV
imaging system and VARiS® practice management solution are registered trademarks of
Varian Medical Systems, Inc. Inspiration™ integrated oncology environment, Millenium™
MLC, VARiS Vision™ oncology information system, Vision™ image management solution,
and TrueBeam™ are trademarks of Varian Medical Systems, Inc.
Microsoft® and Windows® are registered trademarks of Microsoft Corporation.
All other trademarks or registered trademarks are the property of their respective owners.
Copyright © 2008–2014 Varian Medical Systems, Inc.
3
Contents
INDEX .........................................................................................................................................................53
Contents 5
Chapter 1 Introduction
Visual Cues
This publication uses the following visual cues to help you find information:
WARNING: A warning describes actions or conditions that can result in serious injury or
death.
CAUTION: A caution describes hazardous actions or conditions that can result in minor or
moderate injury.
NOTICE: A notice describes actions or conditions that can result in damage to equipment
or loss of data.
Note: A note describes information that may pertain to only some conditions, readers, or sites.
Tip: A tip describes useful but optional information such as a shortcut, reminder, or suggestion,
to help get optimal performance from the equipment or software.
1. Go to http://my.varian.com.
2. Click Contact Us at the top of the window to display customer support and
training options, and international e-mail addresses and telephone numbers.
3. Choose an option:
■ If you do not already have an account, click Create New Account and follow
the instructions. Establishing an account may take a few days.
■ If you have an account, go to the next step.
4. Enter your user name and password.
5. Browse the information and then click the link that corresponds to what you
want to do:
■ Fill out and submit a support request.
■ Find documents. Online documents in PDF format include customer technical
bulletins (CTBs,) manuals, and customer release notes (CRNs).
■ Send an e-mail to Varian support. You can browse for international e-mail
addresses and telephone numbers by geographic area, and for oncology-
specific contacts such as for brachytherapy.
■ Find parts and services by geographical area.
E-Mailing Varian
Send e-mail inquiries through the my.varian.com website.
Alternatively, you can use a support e-mail address that corresponds to your location
or interest:
Location E-mail Address
North America support-americas@varian.com
Latin America soporte.al@varian.com
Europe support-emea@varian.com
Chapter 1 Introduction 7
Location E-mail Address
Australia and New Zealand support-anz@varian.com
China support-china@varian.com
Japan support-japan@varian.com
South East Asia support-sea@varian.com
Brachytherapy Systems brachyhelp@varian.com
Related Publications
Varian recommends also referring to the following user documentation on the
specifics of system operation, or for background information depending on system
version:
■ ARIA RTM DICOM Import and Export Reference Guide
■ ARIA RTM Workflow Management Reference Guide
■ ARIA RTM Workflow Management Online Help
■ ARIA RTM RT Chart Reference Guide
■ ARIA RTM RT Summary Reference Guide
■ ARIA RTM Dosimetric Review Reference Guide
■ ARIA RTM Treatment Preparation Reference Guide
■ Treatment Delivery Instructions For Use
■ 4D Integrated Treatment Console Reference Guide
■ 4D Integrated Treatment Console Customer Release Note
■ 4D Integrated Treatment Console Administration Reference Guide
■ On-Board Imager Reference Guide
Chapter 1 Introduction 9
■ On-Board Imager Customer Release Note
■ TrueBeam Technical Reference Guide—Volume 2: Imaging
Varian has also made many items of documentation available on the MyVarian
website.
ARIA users may freely register for access at:
http://my.varian.com/
General
Your hospital is responsible for establishing emergency and safety procedures to
ensure safe operation and maintenance conditions.
The process of delivering radiation therapy contains potentially life-threatening risks
to patients, operators and bystanders. Be sure to read and understand all safety
information before operating machinery and delivering treatment.
Varian hardware and software are designed to meet current international safety
standards, including IEC, for the protection of patients and operators.
However, hazards and risks cannot be ruled out completely. You must follow the
instructions and procedures described in the manuals.
Any use of the system and software which does not comply with the agreed use
described in this manual or other related Varian manuals is prohibited.
Modifications to the software are prohibited.
WARNING: Incorrect use of a radiotherapy linear accelerator can cause serious injury or
death. Only trained personnel under the supervision of a licensed physician should be
authorized by the hospital or owner to operate a clinical accelerator. The emergency
and safety procedures are described in the corresponding Instructions for Use.
Chapter 2 Safety 11
■ No modifications to the system are permitted without prior review and approval
from Varian.
Note: It is vitally important that the export preparation of the DICOM RT data occurs before
the downtime.
DICOM
ARIA .dcm
Export
DB
4D Console
DICOM
DICOM RT Mode
Import
.dcm
■ System upgrade from VARiS Vision to ARIA, see Figure 3 Upgrade from VARiS
Vision to ARIA on page 15.
DICOM .dcm
V7.x Export
DB
4D Console
DICOM RT Mode
DICOM ARIA
.dcm Import DB
CT Image
These files have the prefix CT. A single image (CT slice) is around 0.5 MB in size. A
CT volume containing 100 slices would therefore be around 50 MB in size. A single
planning volume image consists of many individual slices. In this context, CT images
are only needed by OBI for either Marker Match or the 3D-3D use cases.
RT Plan
These files have the prefix RP. A single plan file is typically a few kB in size, but can
increase to around 1 MB if all fields use dynamic MLC. Plan files contain information
on the relevant fields, MU and reference points. The field data within the plan also
have information on beam accessories, such as MLC (static or dynamic), wedges and
blocks. An example of a DICOM RT plan file name is:
RT ION Plan
These files have the prefix RN. A single plan file is typically a few kB in size. Plan files
contain information on the relevant fields, MU and reference points. The field data
within the plan also have information on beam accessories, such as snouts, wedges
and blocks. An example of a DICOM RT ION plan file name is:
RN.1.2.246.352.71.5.330622248013.132.20110120155231.dcm
RT Image
These files have the prefix RI. A single DRR image file is typically around 0.5 MB in
size, a single fluoroscopy or kV image is typically between 1.5 MB and 6 MB,
depending on imaging system resolution. 2D or 3D image files contain the pixel
information of the image, as well as the drawing layer and contour information.
Examples are DRR or simulator fluoroscopy images. RT images can also be the 2D or
3D images acquired from a treatment session (for example, individual MV portal
images).
RT Spatial Registration
These files have the prefix RE. A spatial registration file is typically around 35
kilobytes in size. The spatial registration file contains positional information and is
used internally for pairing images together for subsequent off-line review.
RT Structure
These files are related to CT volume images and have the prefix RS. The size of the
file depends on the number and complexity of structures in the original image. A
structure file can therefore easily end up being more than 1 MB in size. In this
context, CT images are only needed by OBI for either Marker Match or the 3D-3D use
case. During 3D-3D use cases, a further RS file is created by the system that contains
the CBCT isocenter information (~10 kilobytes).
RT Treatment History
These record files have the prefix RT. Each treatment history file is typically around 3
kB in size. A single history record represents a single field exposure made at the
accelerator. The RT Treatment History File is created after the patient is treated in
DICOM RT Mode. One file exists for each field treated.
Overview
The basic steps when using DICOM RT Mode are:
■ File Storage Preparation on page 20
■ Prepare the Machine and Imaging Environment for OBI 1.4, 1.5, and 1.6 on
page 23
■ Configure Import and Export Filters on page 25
■ Export DICOM Data in ARIA 8.0 to 10.0 on page 27
■ Export DICOM Data in ARIA 11 or ARIA RTM 13 on page 33
■ DICOM RT Data on 4DITC on page 36
■ Import DICOM Records to the ARIA 11 or ARIA RTM 13 Database on page 43
Storage Space
Ensure that you have sufficient storage space for the initial DICOM data.
Note: Ensure that the file is organized logically around each patient. Create suitably named
folders before performing the DICOM RT export using Windows Explorer.
Where several plans exist for treatment or imaging, allocate them to individual
subfolders, along with any reference images.
For export to OBI 1.4 and 1.5 (Advanced Imaging), use a shared folder on the 4DITC
workstation. The shared folder will be used by the DICOM Stream Service of the OBI
workstation to transfer the relevant data into and out of OBI.
Figure 5 Shared Folder on 4DITC workstation on page 21 shows an example of
such a shared folder on the 4DITC workstation. In this example, the shared folder is
called: D:\DICOM RT
Note: Discuss this possibility with Varian Service staff in advance of downtime during an
upgrade.
Note: Note that the CBCT data is saved separately to the main file store for the DICOM RT
Plan/Ref Images/Structures.
1. Ensure that the device is inserted and recognized by Windows, when using an
external storage device for the file storage system.
2. Log into RT Chart.
3. Select the Import Export workspace.
4. Choose Tools > Import Export Configuration.
5. Click Add in the Export Filter area.
6. Select DICOM Media File Export Filter.
7. Select the Make The Filter Available For The Entire Site check box to make the
export filter accessible from all workstations.
If you leave this unchecked the export filter is only available from that individual
workstation.
8. Click Add .
9. Change the ID of the filter from the default as needed; for example, DICOM RT
Export For 4DITC.
10. Click Browse.
Note: Use individual patient-based folders in the file storage system, rather than saving all
files to a single folder. Such folders can be identified using the ID1 +/- Patient Name labels.
12. Always use the Object UID for the default file name creation, otherwise users will
encounter problems with the loading of file data to 4DITC.
13. Click OK.
14. Click Close after the filter is configured.
1. Ensure that the device is inserted and recognized by Windows when using an
external storage device for file storage.
2. Choose User Home > Quicklinks > DICOM > Import Export.
3. Click Manage in the Filter Selection panel.
4. Click Add in the Export Filter area.
5. Select DICOM Media File Export Filter.
6. Select the Shared check box to make the export filter accessible from all
workstations.
If you leave this unchecked the export filter is only available from that individual
workstation.
7. Click Add.
8. Change the Name of the filter from the default as required; for example, DICOM
RT Export For 4DITC.
9. Click Browse.
Note: Note: For further information on the DICOM Import Export application, refer to the
DICOM Import and Export Reference Guide, as well as the ARIA RTM Workflow
Management Reference Guide and the ARIA RTM Workflow Management Online Help.
For OBI 1.4 and 1.5 (Advanced Imaging) imaging, place the DICOM data into the
shared folder on the 4DITC workstation in the file storage system, see Figure 5
Shared Folder on 4DITC workstation on page 21.
1. Ensure that the device is inserted and recognized by Windows, when using an
external storage device for the file storage system.
2. Start RT Chart workspace.
3. Select the Scheduling workspace.
4. Open the desired patient and select a course context.
5. Verify that the desired sequence image template information has been applied to
the next active session for the plan. This also applies for OBI imaging.
Note: Only the image template information for the next active session is exported.
Note: If you plan to use multiple or varying plans during OIS downtime, make a manual
note of the plan scheduling and ordering.
Note: In ARIA versions of RT Chart you can set treatment approval only in the Reference
Point workspace.
Note: The previous step applies only to ARIA versions 8.6 - 10.0.
11. With the plan context selected, choose File > Export > Wizard.
12. Verify that the Plan check box is selected.
13. Click Next.
a. If there are only treatment fields in plan (no imaging), choose the settings as
shown in Figure 11 Treatment Fields Only in Plan / No Imaging - MV
Imaging on page 32.
b. If there are only treatment fields in plan (MV imaging), choose the settings as
shown in Figure 11 Treatment Fields Only in Plan / No Imaging - MV
Imaging on page 32.
c. If there are only setup fields in plan (MV or kV imaging), choose the settings
as shown in Figure 12 Mix of Treatment and Setup Fields in Plan (No
Imaging / MV imaging / MV or kV imaging on page 32.
d. If there is a mix of treatment and setup fields in plan (no imaging), choose the
settings as shown in Figure 12 Mix of Treatment and Setup Fields in Plan
(No Imaging / MV imaging / MV or kV imaging on page 32.
e. If there is a mix of treatment and setup fields in plan (MV or kV imaging),
choose the settings as shown in Figure 12 Mix of Treatment and Setup
Fields in Plan (No Imaging / MV imaging / MV or kV imaging on page 32.
f. If there is a treatment plan with marker match or 3D-3D (OBI imaging),
choose the settings as shown in Figure 13 Treatment of Plan with Marker
Match or 3D-3D (OBI Imaging) on page 32.
Note:
■ If exporting from ARIA 8.8 for use with an 8.8 (or higher) version of 4DITC, always
enable the option for Compatible To Varian Treatment Consoles 6.5 – 8.6
■ If exporting from ARIA 8.5 or 8.6, always enable the option for Compatible To Varian
Treatment Console.
■ If exporting from earlier versions of ARIA (8.0, 8.1, or 8.2), or from VARiS Vision 7.x,
the same option is named Compatible to Release 6.5. Always enable this option.
CAUTION: At this point, the data is converted to DICOM format. You are notified if
there are any errors or warnings associated with the conversion. Errors always stop the
export process, where as warnings may be less serious.
Note: Except for this case, always consult with the system administrator, if either errors or
warnings are encountered!
Note: Any failures in export must be reported to the system administrator before the OIS
database goes offline, otherwise data will not be available for treatment. If the export is
successful, a message box opens, stating
All Objects Saved Successfully
.
25. Repeat this procedure for any additional plans which also need to be made
available during the downtime period.
Note: For OBI 1.4 and 1.5 the export can initially be carried out to a portable file system (for
convenience). The data must then be loaded to the shared 'DICOM RT' folder on the 4DITC
workstation, before imaging and treatment starts.
Figure 12 Mix of Treatment and Setup Fields in Plan (No Imaging / MV imaging / MV or kV
imaging
1. If using an external storage device for the file storage system, ensure that the
device is inserted and recognized by Windows.
2. Navigate using Quicklinks to Plan Scheduling workspace.
3. Open the desired patient and select a course context.
4. Verify that the desired sequence image template information has been applied to
the next active session for the plan. This also applies for OBI imaging.
Note: Only the image template information for the next active session is exported.
Note: Make a manual note of the plan scheduling and ordering where either individual or
multiple plans are used during downtime.
5. Verify that the desired approval status of the plan is set to Treatment Approved.
If not already set, go to Reference Point workspace and change plan status to
treatment approved.
6. Navigate to Plan Parameters workspace to verify that there are no other
outstanding warnings. Click Validate.
7. Visually check on the 2D or 3D reference images to ensure that there are no more
than 16 individual drawing contours per image (for example, anatomical lines or
points).
For online match or other match with OBI first pre-mark the reference anatomy
on the reference images. Ensure that a field aperture contour is present on the
relevant reference images for a non-OBI 4DITC, in case of online matching.
8. Select the Import Export workspace.
Note: By default you start in the working directory folder which is defined as default for this
filter.
CAUTION: At this point, the data is converted to DICOM format. You are notified if
there are any errors or warnings associated with the conversion. Errors always stop the
export process, where as warnings may be less serious.
Note: If the Administration option for Enable Plan Integrity Checking is disabled on the
system, a warning message at Plan export is displayed. Example: if exporting a Plan with
ID= PELVIS, this warning would be seen as:
Plan 'PELVIS' is treatment-approved but lacks plan
integrity checksum.
For this configuration the warning can be acknowledged by the user (click YES to
continue). Except for this case, always consult with the system administrator, if you
encounter any errors or warnings!
15. Check the export summary table in the Summary panel.
Note: Report any export failures to the system administrator before the OIS database goes
offline, otherwise data will not be available for treatment.
17. Repeat this procedure for any additional plans which also need to be made
available during the downtime period.
Note: If plan changes are done in ARIA after the plan had been exported, the changes might
result in a different Plan UID. In this case the plan must be reexported to avoid confusion
with different plan UIDs for the same plan.
Note: For OBI 1.4 and 1.5 the export could initially be carried out to a portable file system
(for convenience). The data must then be loaded to the shared 'DICOM RT' folder on the
4DITC workstation, before imaging and treatment starts.
CAUTION: Always verify that the correct patient and plan data are loaded to 4DITC. The
Patient Identification pane in 4DITC should be displayed whenever plan data is loaded.
Although patient photos are not supported in DICOM RT Mode, the patient's
name, ID1, ID2, DOB and Oncologist information is still displayed.
CAUTION: Each clinic is responsible for ensuring that users of DICOM RT Mode are aware
of these limitations, before delivering any treatments.
For specific information on the usage of 4DITC or OBI, refer to the following Varian
manuals and documentation:
■ Treatment Delivery Instructions For Use
■ 4D Integrated Treatment Console Reference Guide
■ On-Board Imager Reference Guide
Note: If it becomes necessary to resume a partial dynamic MLC, you can use the Clinac and
MLC Workstation in conventional standalone mode (RV interface off) to set up a
corresponding partial beam.
CAUTION: Care must be taken to ensure that the operators manually select the correct
partial treatment parameters.
■ Plan modifications made in 4DITC result in a new session plan file being created in
the file storage system when the patient data is closed. This session plan does not
automatically overwrite the existing occurrence of the original (RP.) plan file. The
use of plan modifications is not generally recommended with DICOM RT Mode.
■ Continuous acquisition (cine) imaging is only possible by having the correct
sequence template applied before exporting from RT Chart. This template cannot
currently be applied directly from 4DITC.
■ To export 2D or 3D reference images from the Import Export workspace, use the
object UID option in the export filter. Do not use the Patient ID + Object Suffix
export option. If the image file names are not set with the Object UID, the images
do not load to 4DITC (although treatment delivery and image acquisition are still
possible). Similarly, images do not load to 4DITC if they are manually renamed
from the object UID to some other user-defined file name (for example, if the file
name is manually changed to ANT PELVIS IMAGE.dcm). 2D or 3D reference
images must always reside in the same folder (directory) as the related RT plan
RP file. Otherwise, 4DITC will not be able to locate them. Solution: Re-export the
RT plan and 2D or 3D reference image data from the Import Export workspace
using the option for the Object UID in the export filter. Do not manually change
the automatically created filenames. Both the plan and images must be saved to
the same folder (directory). Ensure that the OIS database is still online and
accessible.
Note: For VarisVision Version 6.5 - ARIA 10: RT plan file data exported from the Import
Export workspace must be set to Compatible To Varian Treatment Console. Otherwise, a
message box stating Session Load Error opens in 4DITC whenever you attempt to
open an RT plan file. Click Details << to view details. For an example, see Figure 18
Session Load Error on page 41.
Solution: Ensure that the option for Compatible To Varian Treatment Console is
selected and re-export the RT plan and 2D or 3D reference image data from the
Import Export workspace.
CAUTION: To minimize confusion, do not make plan changes during DICOM RT sessions.
Avoid opening a Session plan file using DICOM RT Mode for future treatment. Stick to
using the original RP plan file.
Option 1: 1. In the Tools menu, clear the DICOM RT Mode check mark.
2. Click Open Patient to access the queue.
Option 2: ■ Exit from 4DITC and reopen the application.
The normal function to open patients from the queue is restored by
default when 4DITC is restarted.
Note: Ensure that the import of patient DICOM RT history and imaging data to the ARIA
database is done before any subsequent treatments are delivered.
Import RT Records
There are several possibilities to perform actions or generate data in DICOM RT
Mode. The following example follows the import of a pelvis treatment plan. Use it as
a guide.
Prerequisites:
■ System upgrade. ARIA database is shutdown.
■ Required filters and user rights are defined by the system administrator.
■ A treatment plan including Setup Fields has been scheduled for a total of 30
sessions.
■ The plan was applied in DICOM RT Mode and Images were acquired respectively
during each DICOM RT session.
To import treatment records:
1. Navigate from User Home > Quicklinks > DICOM to the Import Export
workspace.
2. Click on the Import tab.
3. From the list of available filters, select the required DICOM Media File Import
Filter.
4. Click Next.
To browse to the desired patient folder that holds the DICOM history data in the
file storage system, click the browser button.
Note: Inform the system administrator of any errors or warnings before proceeding!
The wizard matches up the patient defined in the DICOM files against the
corresponding patient in the ARIA database.
After successful patient matching, patient data is listed in the Patient Selection
Panel
a. Choose one entry in the Existing Patients list on the left side.
b. If the patient matching fails, click New Patient or Browse Patients.
The Patient Explorer application opens and you can search for patients or
create a new patient record. For detailed information, refer to the Patient
Explorer online help. A new patient is listed in the Existing Patients list.
c. Highlight the patient.
8. Click Next.
After the import is completed, you need to verify the import and verify the
scheduling in Treatment Preparation, see Verify and Complete the Import on
page 47 and Verify the Scheduling in Treatment Preparation on page 51.
The Import Export Log displays the alerts to problems that occurred during import.
An overview of the objects imported to the selected target patient is displayed in the
Connection panel.
Note: If there are no error or warning messages, proceed with the next step.
Note: For verifying the scheduling, see Verify the Scheduling in Treatment Preparation
on page 51.
A display for editing fraction numbers opens. Under Select the treatment
records to be updated check the treatment records which share the same fraction
number. The Type column indicates, that the treatment record is imported.
7. Enter a new value for the fraction number in the Change to field.
CAUTION: Take care to assign fraction numbers in the proper order. Otherwise you may
end up with confusing names and with wrong predictions about the numbering of
future fractions.
8. Click Save.
The course timeline displays the updated fraction number.
Note: Note: For more detailed information on the RT Summary Workspace, please refer to
the ARIA RTM RT Summary Reference Guide.
Note: For more detailed information refer to ARIA RTM Treatment Preparation Reference
Guide.
Index 53
RT plan 28 Linac Verification Interface (LVI) 8
Export DICOM Data in ARIA 11 / ARIA RTM LVI (Linac Verification Interface) 8
13 33
export DICOM data in ARIA 8.0 to 10.0 27
export filter M
configuring 25, 26 Megavolt (MV) 8
Export Filter for ARIA 11 / ARIA RTM 13 26 message box
do you want to close the patient 41
management system error 39
F MLC (Multileaf Collimator) 8
file storage system modal mode
preparing 20 DICOM RT Mode Workflow 27
filter 25, 26 modification 42
fraction 42 modify the OIS database plan after initial plan
number 50 export 36
Monitor Unit (MU) 8
MU (Monitor Unit) 8
G Multileaf Collimator (MLC) 8
guide MV (Megavolt) 8
intent 6 my.varian.com 7
purpose 6
target group 6
N
number
H session 50
history file 41
from 4DITC 42
O
OBI (On-Board Imager) 9
I OIS
ID (Identifier) 8 planned downtime 14
Identifier (ID) 8 unplanned downtime 14
image file 9 OIS (Oncology Information System) 9
2D 39 On-Board Imager (OBI) 9
import Oncology Information System (OIS) 9
RT treatment record 45 online customer support 7
wizard (figure) 45 open patient plan 36
Import / Export workspace 13 open RT plan 36
Import Filter for ARIA 11 / ARIA RTM 13 26 open RT plan data from the file storage system
information update 36 36
intent of guide 6 operating procedure 20
ordering product documents by phone 7
organization of patient data 21
K OSP 9
kV (kilovolt) 8
P
L patient data
limitation closing 41
for treatment 38 Patient Explorer application 46
S
settings for the Export Wizard (RT Chart /
ARIA 8.8) 32
starting treatment 38
storage space 20
Index 55