Evidence map›Paper›PMID 38748947›Full record

ArticleJCO precision oncology2024

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

Ray Manneh, Carmen Alaez Verson, Angel Martin, Arturo Delgado, Pedro H Isaacsson Velho, Alejandro Manduley, Luis Tejado, Yolanda Rodríguez, Carmen Vargas, Pedro C Barata

Abstract readMulticenter Study
In one paragraph

Article in JCO precision oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. The Genetic and Molecular Analyses of Rare Candidate GermlineInternational journal of molecular sciences · 2026
    Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Ray MannehSociedad de Oncología y Hematología del Cesar, Valledupar, Colombia.ORCID 0000-0002-8106-9741
Carmen Alaez VersonLaboratorio de Diagnóstico Genómico, Instituto Nacional de Medicina Genómica, Ciudad de Mexico, Mexico.ORCID 0000-0003-1042-8505
Angel MartinInstituto Alexander Fleming, Buenos Aires, Argentina.ORCID 0000-0002-1463-8887
Arturo DelgadoCentro Médico Nacional Siglo XXI, Ciudad de Mexico, Mexico.
Pedro H Isaacsson VelhoHospital Moinhos de Vento, Porto Alegre, Brazil.ORCID 0000-0002-3117-7031
Alejandro ManduleyCentro de Especialidades Urológicas de Panama, Panama City, Panama.
Luis TejadoAstraZeneca, Ciudad de Mexico, Mexico.ORCID 0000-0003-3790-8314
Yolanda RodríguezAstraZeneca, Ciudad de Mexico, Mexico.
Carmen VargasAstraZeneca AG, Baar, Switzerland.ORCID 0000-0003-4834-7305
Pedro C BarataUniversity Hospitals Seidman Cancer Center, Cleveland, OH.ORCID 0000-0002-8890-2951

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe 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

methodsThis 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.

resultsBetween 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

conclusionDespite 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.

Indexed as

MutationProstatic Neoplasms, Castration-ResistantRecombinational DNA RepairAgedAged, 80 and overCross-Sectional StudiesHumansLatin AmericaMaleMiddle AgedPrevalenceProspective Studies

Identifiers

PMID38748947
PMCPMC11371117

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.