Trial Evaluating the Safety and Efficacy Of MR-Linac-Guided Radiotherapy as Salvage Treatment After External Beam Radiotherapy Recurrence (TUMORNATOR II)
Summary
The purpose of this study is to assess the impact of prostate-specific membrane antigen/positron emission tomography (PSMA/PET)-informed magnetic resonance (MR)-guided radiation therapy on serious toxicity outcomes in patients with biopsy-proven locally radiorecurrent prostate cancer. The primary aim is to evaluate the safety of delivering MR-Linac-guided stereotactic body radiotherapy (SBRT) after prior prostate external beam radiotherapy for recurrent disease, and assess urinary toxicity outcomes at 2 years.
Arms & interventions
- RadiationStereotactic Body Radiation Therapy (SBRT)
SBRT will be delivered with a prescription dose of 8 Gy x 5 fractions prescribed to the 95% isodose line encompassing the dominant recurrent intraprostatic lesion (DRIL) as seen on MRI and/or PET PSMA imaging plus 4mm (GTV+4mm=CTV\_40). Remainder of the prostate gland minus CTV\_40 (CTV\_25) will be prescribed to 5 Gy x 5 fractions at the 95% isodose line.
- DrugAndrogen Deprivation Therapy (ADT)
ADT would be given 0-1 months prior to planned SBRT to the prostate for total of 4-6 months. ADT will be administered via Leuprolide or Degarelix monthly injections or daily Relugolix pills.
Outcome measures
Primary
Late toxicity (after 90 days) radiation-associated genitourinary (GU) and gastrointestinal (GI) events
A serious toxicity event will be defined as any Grade 3 or higher genitourinary or gastrointestinal toxicity, based on NCI CTCAE v5.0.
Time frame: Month 24
Secondary
Acute toxicity (occurring within 90 days of the treatment) radiation-associated genitourinary (GU) and gastrointestinal (GI) events
Time frame: Month 24
Biochemical progression free survival
Time frame: Month 24
Distant metastasis-free survival (DMFS)
Time frame: Month 24
Radiographic treatment response rate of target intra-prostatic lesion
Time frame: Month 24
Expanded Prostate cancer Index Composite (EPIC-26) Short Form score
Time frame: Month 24
International prostate symptom score index (IPSS) score
Time frame: Month 24
International Index of Erectile Function (IIEF) score
Time frame: Month 24
Eligibility criteria
Study locations (1)
NYU Langone Health
New York, New York, 10016