Metastasis-directed Radiotherapy (MDRT) for Men With De-novo Oligometastatic Prostate Cancer Treated With Long-term Androgen Deprivation Therapy in the STAMPEDE Trial (METANOVA)
Summary
The purpose of this study is to find out if giving radiation therapy (RT) to areas of metastatic prostate cancer at the time a participant is diagnosed will help control disease better than the usual treatment. This treatment is called metastasis-directed radiotherapy (MDRT). The usual treatment for prostate cancer that has spread to other parts of the body is to give lifelong treatment with hormone therapy (also known as androgen deprivation therapy or ADT). Participants may also be given prostate RT even if the disease is metastatic. Participants will receive hormone therapy (the standard treatment for prostate cancer) for 12 months. The hormone therapy agents may be taken by mouth or given as an injection. Participants will also have prostate RT. Up to 50 participants will have surgery to remove the prostate instead of having prostate RT. A portion of the participants will be randomized to receive MDRT to areas where the cancer has spread. For participants who have surgery to remove their prostate, they will be asked to allow tissue samples collected during the surgery to be sent to an outside lab for research tests and extra blood samples drawn for research tests before starting the study, and at the time the cancer becomes worse if applicable. Participation in the study will last approximately 12 months, and will be followed by their doctor for up to five years per standard of care. The main goal is to compare the efficacy of the standard of care (standard systemic therapy + definitive prostate-directed local therapy) versus the standard of care with metastasis-directed radiotherapy (MDRT) for consolidation of metastatic disease.
Detailed description
Prostate cancer (PCa) is the most common cancer in men worldwide, with 10% diagnosed with metastatic disease at the time of presentation. The metastatic capacity of cancers behaves along a spectrum of disease progression, such that some solid tumors have spread widely before clinical detectability and others never metastasize. While metastatic disease has historically been treated with palliative intent, an oligometastatic state where metastases are limited in number and location has emerged in which participants with oligometastatic disease may benefit from effective local therapy in addition to systemic therapy. Systemic standard-of-care therapies often include androgen deprivation therapy (ADT) and Androgen receptor signaling inhibitor (ARSI). Studies have shown that administering local radiotherapy (RT) to the prostate in addition to standard of care may improve radiographic profession-free survival. It may be even more efficacious to add metastasis-directed radiotherapy (MDRT) to the treatment of oligometastatic prostate cancer cases. More research is necessary to investigate the application of MDRT to improve disease control.
Arms & interventions
- DrugAndrogen deprivation therapy (ADT)
Standard androgen deprivation therapy (ADT) will be administered at the discretion of treating physician.
- DrugAndrogen receptor signaling inhibitor (ARSI)
Standard androgen receptor signaling inhibitors (ARSI) will be administered at the discretion of the treating physician.
- OtherLocal Therapy: Radical Prostatectomy (RP) or Radiotherapy (RT)
Local therapy will either be radiotherapy (RT) or radical prostatectomy (RP). * Prostate +/- pelvic nodal radiation * Radical prostatectomy + pelvic lymph node dissection
- RadiationMetastasis directed radiotherapy (MDRT)
In participants randomized to the MDRT arm, MDRT to all lesions will be performed by the end of Week 24. Selection of a particular regimen (the dose and fractionation) will based on the size and location of the participant's metastatic site and the surrounding normal tissue constraints.
Outcome measures
Primary
Failure-free survival (FFS)
Failure-free survival, defined as time from randomization to first evidence of at least one of: biochemical failure; progression either locally in lymph nodes, or in distant metastases; skeletal related event (where confirmed disease progression);any salvage intervention (local or systemic) required after 12m of planned SOC therapy; or death from prostate cancer. Biochemical failure, based on the PSA nadir in the first 24 weeks after randomization, is defined as at least one of: post-RT: 1. as per the Prostate Cancer Clinical Trials Working Group 3 (PCWG3), where PSA must rise by ≥ 25% and ≥ 2ng/mL above nadir, confirmed by progression at two time points at least 3 weeks apart 2. post-RP: serum PSA nadir + 0.4 ng/mL, requiring confirmation ≥4 weeks later
Time frame: Up to 5 years from treatment
Secondary
Overall survival (OS)
Time frame: Up to 5 years from treatment
Radiographic progression-free survival (rPFS)
Time frame: Up to 5 years from treatment
Time-to-next-intervention (TTNI)
Time frame: Up to 5 years from treatment
Time-to-castration-resistant prostate cancer
Time frame: Up to 5 years from treatment
Prostate-specific cancer mortality (PCSM)
Time frame: Up to 5 years from treatment
Change in EPIC-26 Sexual Domain Score
Time frame: Baseline, 1 year after treatment
Change in EPIC-26 Sexual Domain Score
Time frame: Baseline, 3 years after treatment
Change in EPIC-26 Urinary Domain Score
Time frame: Baseline, 1 year after treatment
Change in EPIC-26 Urinary Domain Score
Time frame: Baseline, 3 years after treatment
Change in EPIC-26 Hormone Domain Score
Time frame: Baseline, 1 year after treatment
Change in EPIC-26 Hormone Domain Score
Time frame: Baseline, 3 years after treatment
Change in EPIC-26 Bowel Domain Score
Time frame: Baseline, 1 year after treatment
Change in EPIC-26 Bowel Domain Score
Time frame: Baseline, 3 years after treatment
Change in IPSS Score
Time frame: Baseline, 1 year after treatment
Change in IPSS Score
Time frame: Baseline, 3 year after treatment
Skeletal-related events (SRE)
Time frame: 5 years after treatment
Eligibility criteria
Study locations (2)
University Hospitals Cleveland Medical Center Seidman Cancer Center
Cleveland, Ohio, 44106
Carbone Cancer Center University of Wisconsin-Madison
Madison, Wisconsin, 53792