Real world (rw) homologous recombination repair (HRR) gene mutation testing trends in patients (pts) with metastatic castrate-resistant prostate cancer (mCRPC) in the United States (US).

Authors

Pedro Barata

Pedro C. Barata

Tulane University, New Orleans, LA

Pedro C. Barata , Rachel Montgomery , Matthew Last , Liane Gillespie-Akar , Jonathan Nazari , Bhakti Arondekar , Alexander Niyazov

Organizations

Tulane University, New Orleans, LA, Adelphi Real World, Bollington, United Kingdom, Pfizer, Inc., New York, NY, Pfizer Inc., Collegeville, PA

Research Funding

Pharmaceutical/Biotech Company
Pfizer Inc

Background: Previous research suggests that HRR mutations may have prognostic value in mCRPC. Additionally, HRR mutations are therapeutically relevant and can inform treatment decisions. Limited information is available on HRR mutation testing rates in the US. This study assessed rw HRR testing patterns in pts with mCRPC in the US and described characteristics associated with HRR testing. Methods: Retrospective data from pts with mCRPC initiating first line (1L) treatment between 2014 – 2021 was obtained from the nationwide Flatiron Health electronic health record-derived de-identified database. Pt demographic and clinical characteristics were summarized descriptively across subgroups by HRR gene testing status (tested vs not tested). A multivariable logistic regression model was used to assess factors associated with receiving HRR testing, and included covariates for demographic, clinical, and treatment characteristics. Results: A total of n=8,166 pts with mCRPC receiving 1L treatment were identified. The mean age of the cohort was 72.9 (standard deviation (SD) 8.1) years. Overall, 2,122/8,166 (26%) were known to have received HRR mutation testing. Pts who did not receive HRR testing were older compared to HRR tested pts (mean age 73.7 (SD 8.5) vs 70.6 (SD 7.5) years). A higher proportion of HRR tested were receiving treatments from an academic medical center vs community practice (14.5% vs. 7.7%). Multivariable logistic regression indicated age > 65 (vs < 65 years), Black race (vs White), being treated in the community (vs academic), and having de novo metastatic disease (vs recurrent) were associated with a statistically significant lower odds of HRR mutation testing. In contrast, a higher socioeconomic status and being diagnosed with mCRPC after 2018 were associated with a statistically significant increased odds of HRR mutation testing. Conclusions: In this rw study, a minority of US pts with mCRPC received HRR mutation testing. Disparities in HRR mutation testing exist, and focused efforts to increase HRR testing should be developed, especially among Black pts, pts with lower socioeconomic status, pts treated in the community setting, and pts > 65 years of age.

Relationship between pt characteristics and HRR mutation testing.

Covariates Odds Ratio (95% CI) P-value
Age > 65 vs <65 0.550 (0.476 –0.635) <0.0001
Black vs White 0.750 (0.619-0.908) 0.0033
Community vs Academic Setting 0.389 (0.309-0.489) <0.0001
Income ≥ $130,734 vs < $31,641 1.468 (1.200-1.797) 0.0002
De novo disease (no vs yes) 0.653 (0.559-0.763) <0.0001
Diagnosis year after 2018 vs before 2018 2.322 (2.088-2.582) <0.0001

Disclaimer

This material on this page is ©2024 American Society of Clinical Oncology, all rights reserved. Licensing available upon request. For more information, please contact licensing@asco.org

Abstract Details

Meeting

2023 ASCO Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session A: Prostate Cancer

Track

Prostate Cancer - Advanced,Prostate Cancer - Localized

Sub Track

Quality of Care/Quality Improvement and Real-World Evidence

Citation

J Clin Oncol 41, 2023 (suppl 6; abstr 98)

DOI

10.1200/JCO.2023.41.6_suppl.98

Abstract #

98

Poster Bd #

D1

Abstract Disclosures