Condition: Glioblastoma (GBM) · Sponsor: Brigham and Women's Hospital
Glioblastoma (GBM) is an aggressive malignancy of the central nervous system. Older adults with GBM have a unique constellation of medical, psychosocial, and supportive care needs. To address these challenges, prior work has evaluated the feasibility of hypofractionation, a treatment approach delivering fewer, larger radiation dosages over a shorter time period. Common hypofractionated regimens deliver a lower biologically equivalent radiation dose than the conventional regimens used for younger adults. Whether dose escalated hypofractionation can further improve outcomes in older adults remains unclear. This will be a hybrid randomized control trial comparing the efficacy and safety of dose-escalated and standard hypofractionated radiotherapy among older adults with newly-diagnosed glioblastoma compared to standard three-week course. This research study involves the administration of radiation therapy. Radiation will either be delivered at the standard daily dose or at an increased daily dose over a three weeks course of radiation treatment. Research study procedures will include a screening evaluation to assess eligibility, as well as clinical visits for radiation delivery and to assess symptoms during treatment and at scheduled follow-up times. Participants will be randomly assigned to one of the two arms of the trial: 1. Standard hypofractionated radiation over 3 weeks 2. Dose-escalated hypofractionated radiation over 3 weeks
This description comes directly from the study's public registry record.
Rifaquat Rahman, MD · 617-732-6682 · rrahman@bwh.harvard.edu
Anurag Saraf, MD · 781-624-4700 · anurag_saraf@dfci.harvard.edu
Always discuss trial participation with your own doctor first.
| Brigham and Women's Hospital | Boston, Massachusetts, United States | Recruiting |
| Dana-Farber Brigham Cancer Center, Milford Hospital | Milford, Massachusetts, United States | Recruiting |
| Dana-Farber Brigham Cancer Center, South Shore Hospital | South Weymouth, Massachusetts, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06835803