A Study of MRI-guided High-dose Radiation Therapy in Prostate Cancer (NCT04997018)
๐ฉบ Plain-English Summary (8th-Grade Level)
One of the usual approaches to treating intermediate-risk prostate cancer is a type of radiation therapy called SBRT (stereotactic body radiation therapy). SBRT delivers higher than standard doses of radiation over a lower number of treatment sessions. However, there is a 20% chance that intermediate-risk prostate cancer will come back after this treatment. The purpose of this study is to find out whether giving an even higher dose (a "boost" dose) of radiation directly to the main tumor and the standard dose of radiation to the rest of the prostate may cure the cancer or prevent it from coming back for a longer period of time while causing few side effects.
Who can join: To join this study, participants generally need to meet the listed inclusion criteria (12 items) and avoid the listed exclusions (23 items).
Location: Memorial Sloan Kettering at Basking Ridge (Limited Protocol Activities) โ Basking Ridge, New Jersey
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistCheck every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).
Usually NOT eligible if any of the following apply:
- Exclusion Criteria: Patient will be excluded if they meet any one of the following criteria:
- Gleason score \>7
- PSA \>20
- Prior or concurrent androgen deprivation therapy for prostate cancer MRI findings: suspicious for/probable ECE
- MRI findings: \>2 disease foci identifiable
- Evidence of metastatic disease on bone scan or MRI/CT
- MRI ineligibility due to: the presence of a cardiac pacemaker, defibrillator, or other implanted metallic or electronic device which is considered MR unsafe; severe claustrophobia; inability to lie flat for the duration of the study; etc.
- Metallic implant or device in the pelvis that might distort the local magnetic field and compromise quality of mp-MRI
- Lateral pelvic separation greater than 50 cm and/or anterior-posterior separation greater than 35 cm which are incompatible with MRCAT reconstruction
- Contra-indications to receiving gadolinium contrast
- KPS \< 80
- Pelvic or prostate MRI or CT (MRI preferred) evidence of radiographic T3, T4, or N1 disease
๐ Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.
๐ All Participating Trial Locations (7 Sites)
- Memorial Sloan Kettering at Basking Ridge (Limited Protocol Activities) โ Basking Ridge, New Jersey
- Memorial Sloan Kettering at Monmouth (Limited Protocol Activities) โ Middletown, New Jersey
- Memorial Sloan Kettering at Bergen (Limited Protocol Activities) โ Montvale, New Jersey
- Memorial Sloan Kettering at Suffolk-Commack (Limited Protocol Activities) โ Commack, New York
- Memorial Sloan Kettering at Westchester (Limited Protocol Activities) โ Harrison, New York
- Memorial Sloan Kettering Cancer Center (All Protocol Activities) โ New York, New York
- Memorial Sloan Kettering at Nassau (Limited Protocol Activities) โ Uniondale, New York
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.