Evidence map›Paper›PMID 42898852›Full record

ReviewAJOG global reports2026

Prevalence and spectrum of variants in homologous recombination repair genes in ovarian cancer in Latin America: a systematic review and meta-analysis.

Elizabeth Vargas-Castellanos, Natalia Santiago-Tovar, Luisa Murcia-Soriano, Ariana Patino-Herrera, Rafael Parra-Medina, Julian C Riano-Moreno

Abstract readReview
In one paragraph

Review in AJOG global reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Elizabeth Vargas-CastellanosHospital Universitario Mayor-Méderi (Vargas-Castellanos and Murcia-Sonaiano), Universidad del Rosario. Bogotá D.C., Colombia.
Natalia Santiago-TovarFaculty of Medicine. Universidad Cooperativa de Colombia (Santiago-Tovar and Riano-Moreno), Villavicencio, Colombia.
Luisa Murcia-SorianoHospital Universitario Mayor-Méderi (Vargas-Castellanos and Murcia-Sonaiano), Universidad del Rosario. Bogotá D.C., Colombia.
Ariana Patino-HerreraFaculty of Medicine. Universidad Nacional de Colombia (Patino-Herrera), Bogotá D.C., Colombia.
Rafael Parra-MedinaDepartment of Pathology and Molecular Oncology (Parra-Medina and Riano-Moreno), Instituto Nacional de Cancerología, Bogotá D.C., Colombia.
Julian C Riano-MorenoFaculty of Medicine. Universidad Cooperativa de Colombia (Santiago-Tovar and Riano-Moreno), Villavicencio, Colombia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOvarian cancer is a major cause of gynecologic cancer mortality worldwide, with disproportionately poor outcomes in Latin America (LATAM). Variants in homologous recombination repair genes, especially

objectiveTo synthesize the prevalence and spectrum of pathogenic and likely pathogenic variants in homologous recombination repair pathway genes among LATAM ovarian cancer patients and highlight clinical and research implications. STUDY

designThe review protocol was developed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) and was registered in the international prospective register of systematic reviews (PROSPERO; registration number CRD420251019706). We systematically searched MEDLINE, EMBASE, Scopus, Web of Science, LILACS, Cochrane, and Epistemonikos through April 2025. Eligible studies included LATAM ovarian cancer patients tested with multigene panels covering homologous recombination repair genes beyond

resultsEight studies published between 2017 and 2023, including 442 patients with ovarian cancer from Brazil, Argentina, Mexico, Chile, and Colombia, were included in the systematic review. Following variant curation and reclassification, 7 studies comprising 433 patients and 96 pathogenic/likely pathogenic homologous recombination repair variant carriers were retained for prevalence analysis, yielding a crude prevalence of 22.2%. Pathogenic variants predominated (91.7%), with

conclusionThis first systematic synthesis of homologous recombination repair variants in LATAM ovarian cancer reveals a predominance of Implications for Practice: This systematic review highlights both opportunities and barriers for implementing homologous recombination repair testing in ovarian cancer across Latin America. While

Indexed as

BRCA1BRCA2homologous recombination repairHRR geneLatin Americanon-BRCAovarian cancer

Identifiers

PMID42898852
PMCPMC13679366

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.