Prospective Study of Homologous Recombination Repair Gene Mutation Prevalence in Patients With Advanced Prostate Cancer From Latin America: Challenges and Future Approaches

Author:

Manneh Ray1ORCID,Verson Carmen Alaez2ORCID,Martin Angel3ORCID,Delgado Arturo4,Isaacsson Velho Pedro H.5ORCID,Manduley Alejandro6,Tejado Luis7ORCID,Rodríguez Yolanda7,Vargas Carmen8ORCID,Barata Pedro C.9ORCID

Affiliation:

1. Sociedad de Oncología y Hematología del Cesar, Valledupar, Colombia

2. Laboratorio de Diagnóstico Genómico, Instituto Nacional de Medicina Genómica, Ciudad de Mexico, Mexico

3. Instituto Alexander Fleming, Buenos Aires, Argentina

4. Centro Médico Nacional Siglo XXI, Ciudad de Mexico, Mexico

5. Hospital Moinhos de Vento, Porto Alegre, Brazil

6. Centro de Especialidades Urológicas de Panama, Panama City, Panama

7. AstraZeneca, Ciudad de Mexico, Mexico

8. AstraZeneca AG, Baar, Switzerland

9. University Hospitals Seidman Cancer Center, Cleveland, OH

Abstract

PURPOSE The prevalence of homologous recombination repair gene mutations (HRRm) in patients with metastatic castration-resistant prostate cancer (mCRPC) in Latin America and the Caribbean (LAC) is unknown. Prevalence of homologous Recombination repair (HRR) gene mutatiOns in patientS with metastatic castration resistant ProstatE Cancer in LaTin America (PROSPECT) aimed to determine this prevalence and to describe the demographic and clinical characteristics of the participants. MATERIALS AND METHODS This was a prospective, cross-sectional, multicenter study across 11 cancer centers in seven LAC countries. After informed consent, all eligible participants underwent genomic testing by provided blood samples for germline HRR testing; they also provided PC tissue blocks if available for somatic HRR testing. RESULTS Between April 2021 and April 2022, 387 patients (median age, 70 years [49-89], 94.3% Eastern Cooperative Oncology Group 0-1) with mCRPC were enrolled in the study. Almost 40% of them had a family history of cancer, and the overall time from their initial PC and mCRPC diagnosis was 3 years and 1 year, respectively. The overall prevalence of germline HRRm was 4.2%. The mutations detected included the genes CHEK2 (n = 4, 1%), ATM (n = 3, 0.8%), BRCA2 (n = 3, 0.8%), BRIP1 (n = 2, 0.5%), RAD51B (n = 2, 0.5%), BRCA1 (n = 1, 0.3%), and MRE11 (n = 1, 0.3%). The prevalence of somatic HRRm could not be assessed because of high HRR testing failure rates (79%, 199/251) associated with insufficient DNA, absence of tumor cells, and poor-quality DNA. CONCLUSION Despite the study's limitations, to our knowledge, PROSPECT was the first attempt to describe the prevalence of HRRm in patients with PC from LAC. Notably, the germline HRRm prevalence in this study was inferior to that observed in North American and European populations. The somatic HRR testing barriers identified are being addressed by several projects to improve access to HRR testing and biomarker-based therapies in LAC.

Publisher

American Society of Clinical Oncology (ASCO)

Reference31 articles.

1. Global Cancer Observatory. GLOBOCAN 2020. International Agency for Research on Cancer, WHO. 2023

2. Department of Economic and Social Affairs. World Population Ageing 2019. United Nations. 2019

3. The Association Between Age, Prostate Cancer Risk, and Higher Gleason Score in a Long-term Screening Program: Results from the Göteborg-1 Prostate Cancer Screening Trial

4. Optimizing the treatment of metastatic castration-resistant prostate cancer: a Latin America perspective

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