(UroToday.com) The 2025 ASCO annual meeting featured a prostate cancer trials in progress session and a presentation by Dr. Steven Blinka discussing the impact of DNA repair genetic alterations identified by circulating tumor DNA on sensitivity to radium-223 in bone metastatic castration-resistant prostate cancer (mCRPC). Selection, timing, and sequencing of therapy for men with bone mCRPC for optimal clinical outcomes is not well-defined. Accordingly, identification of predictive biomarkers for response and outcomes to a given therapy is critical to guide clinical decision-making.
Prior research has demonstrated that a high proportion (up to 25%) of mCRPC patients harbor aberrations in DNA damage repair (DDR) genes. These findings are clinically meaningful given the efficacy of PARP inhibitors in treating a subset of mCRPC patients with DDR defects. Radium-223 acts by delivering high-energy alpha particles selectively to bone metastases leading to double-stranded DNA breaks, and retrospective studies have shown that patients with DDR alterations who are treated with radium-223 have an overall survival benefit, improved alkaline phosphatase response, and more commonly complete radium-223 treatment. Therefore, Dr. Blinka and colleagues hypothesize that mCRPC with alterations in DDR genes should be particularly vulnerable to treatment with radium-223 and should be evaluated for resultant outcomes prospectively.
This phase 2, multi-center, prospective single-arm biomarker trial is aiming to enroll 60 patients. Eligible patients must have mCRPC, radiographic evidence of bone disease, symptoms, and PSA ≥10 ng/mL to ensure successful ctDNA analysis. All patients will receive radium-223 (55 kBq/kg) for up to 6 doses, and patients who have received prior platinum containing chemotherapy will be excluded. ctDNA will be obtained for OncoPlexCT to determine if a patient has a DDR gene alteration (results will not affect treatment plan), and leukocyte analysis will be performed to confirm whether specific alterations are germline versus somatic.
The primary objective of this study is to determine the response rate of bone mCRPC with DDR deficiency to treatment with radium-223. Response will be defined as having PSA and/or alkaline phosphatase decline of ≥30% from baseline. The null hypothesis is that the true response rate is 0.40, and the alternate hypothesis is the true response rate is 0.80 (TOPARP, NCT01682772). It is estimated that 25% of the patient population will have DDR alterations and outcomes will be compared with those who are DDR proficient. Using 90% power and an alpha of 0.05, this trial will accrue 60 patients to ensure the goal of 12 patients with DDR alterations is met. Secondary objectives include:
- Determining whether patients who received a prior PARP inhibitor have no decrement in response
- Overall survival
- Number of cycles of radium-223 received
- Effect of germline versus somatic alterations on response
This trial is currently open to enrollment at Fred Hutch, the University of Wisconsin, and Johns Hopkins, and 22/60 patients have already been enrolled.
Clinical trial information: NCT04489719.
Presented by: Steven M. Blinka, MD, PhD, Fred Hutchinson Cancer Center, University of Washington, Seattle, WA
Written by: Zachary Klaassen, MD, MSc – Urologic Oncologist, Associate Professor of Urology, Georgia Cancer Center, Wellstar MCG Health, @zklaassen_md on Twitter during the American Society of Clinical Oncology (ASCO) 2025 Annual Meeting, Chicago, IL, Fri, May 30 – Tues, Jun 3, 2025.