Pediatric Cancer Clinical Trial
Official title:
Data Collection of Normal Tissue Toxicity for Proton Therapy for Pediatrics
The goal of this research study is to collect information on the side effects of proton therapy and the details of proton treatment plans so that researchers can develop a method to predict the risk of side effects and to improve the planning and delivery of proton treatment for patients in the future.
If you agree to take part in this study, researchers will gather information about your
treatment and treatment outcomes and store it electronically in a database. By carefully
evaluating the data about your treatment, researchers may improve proton treatment for
patients in the future. There will be no change to your recommended standard of care and
follow-up studies. The treatment information and follow-up information will be stored in a
database. The information will then be available at a later date for researchers to study.
The database will be stored on a secure information network, and only those people who are
involved with this research and who have prior approval from the study doctor will have
access to it.
Researchers will request information from the follow-up visits that you have as part of your
standard of care yearly or more often and test results for at least 10-15 years. The tests
may be performed at other clinics, but MD Anderson researchers will request that the results
be sent to them at MD Anderson.
This is an investigational study. Proton radiotherapy is FDA approved. Researchers hope to
enroll all children who will be treated with proton radiotherapy at MD Anderson on this study
so that as much information as possible will be gathered. Up to 1000 patients will be
enrolled at MD Anderson.
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