RADIATION THERAPY ONCOLOGY GROUP
RTOG 1203
A Randomized Phase III Study Of Standard Vs. IMRT Pelvic Radiation For Post-Operative Treatment Of Endometrial And Cervical Cancer (TIME-C)--RTOG CCOP Study
RTOG 1203
A Randomized Phase III Study Of Standard Vs. IMRT Pelvic Radiation For Post-Operative Treatment Of Endometrial And Cervical Cancer (TIME-C)--RTOG CCOP Study
Protocol Participation Information
- Credentialing - IMRT
- Credentialing Requirements
- Facility Questionnaire: Part I is required for IMRT on this protocol.
-
RPC Phantom Dosimetry Test
- Fill out the RPC Phantom Request Form to request shipment of a phantom.
- Contact Bill Straube at (314) 362-9762 regarding submission of phantom treatment planning data to the ITC.
- Credentialing - Standard RT
- Facility Questionnaire: Part I is required for standard RT on this protocol.
- A test of digital data submission is required for institutions that have not previously submitted external beam treatment planning data to the ITC. The treatment planning system to be used to plan patients on the study should be used for this digital data submission test. Please contact the ITC (itc@wustl.edu) for questions regarding digital data submission and to request an SFTP account, if you do not have one already.
- Data Submission
- Please see the RPC website to submit the Gynecological Brachytherapy Protocol Compliance Form. (Click on "Forms" on the homepage, and select Gynecological Brachytherapy Protocol Compliance Form). All optional brachy data, including hard copy film, as well as full AND empty bladder scans are to be mailed directly to the RPC. Call 713-745-8989 with any questions.
- Digital Data Submission Procedures
- Digital Data Submission Information (DDSI) Form
- ATC Compliant Treatment Planning Systems
- Structure Names - Please refer to protocol text for structure naming requirements.
- Gynecologic Pelvis Atlas
- Protocol Information (http://www.rtog.org/)
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