drugset / Trial / NCT07645326

RISK-ADAPT Protocol in Metastatic Hormone-Sensitive Prostate Cancer (mHSPC)

NCT07645326

Phase 2 Not yet recruiting 108 enrolled Georgetown University Lantheus Medical Imaging · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a prospective, interventional, non-randomized, phase 2 study to assess oncologic outcomes of metastatic hormone-sensitive prostate cancer (mCSPC) patients who receive a risk-adapted treatment approach followed by treatment de-escalation at the Medstar Health network. A pragmatic design will be implemented in order to make the study available to patients at greatest needs from minority populations in the community. Additional assessments include quality-of-life (QoL) and sexual function changes as well as correlative studies. A maximum of 108 patients will be enrolled in this study. The investigators hypothesize that with a risk-adapted treatment approach followed by treatment de-escalation, more than 50% of patients will have radiographic progression-free survival (rPFS) at 36 months. Additionally, the investigators hypothesize that the risk-stratified de-escalation approach will result in fewer treatment-related adverse events and better QoL, compared to historical controls.

Timeline

Start
2026-08
Primary completion
2032-08
Completion
2032-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Abiraterone acetate Small molecule
Subject Apalutamide Small molecule
Subject Darolutamide Other / unclassified
Subject Docetaxel Small molecule
Subject Enzalutamide Other / unclassified