DNA-Damaging Therapies in Patients With Prostate Cancer and Pathogenic Alterations in Homologous Recombination Repair Genes

Patients with <i>BRCA1/2</i>-mutated PC had significantly improved outcomes to PARPi but not platinum chemotherapy compared with those with HRR mutations without direct BRCA complex interaction.

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Publication Details

Journal
JCO Precision Oncology
Published
2024-08-01
DOI
https://doi.org/10.1200/po.24.00014
Citations
7
Primary Topic
PARP inhibition in cancer therapy
Type
article
Field-Weighted Citation Impact
1.98

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article

DNA-Damaging Therapies in Patients With Prostate Cancer and Pathogenic Alterations in Homologous Recombination Repair Genes

Matthew Labriola, Michael Thomas Schweizer, Laura Graham, Olesia Kellezi et al.
7 citations
JCO Precision Oncology
PARP inhibition in cancer therapy
1.98
article

DNA-Damaging Therapies in Patients With Prostate Cancer and Pathogenic Alterations in Homologous Recombination Repair Genes

Matthew Labriola, Michael Thomas Schweizer, Laura Graham, Olesia Kellezi, Vadim S. Koshkin, Andrew J. Armstrong, Ajjai Alva, Clara Hwang, Mehmet Asım Bilen, Rohan Garje, Pedro Coelho Barata, Deepak Kilari, Rana R. McKay, George Mo, Vaibhav G. Patel, Shoshana Rothstein, Abhishek Tripathi, Michael Pierro, Bicky Thapa, Tanya Barauskas Dorff, Joseph J. Park, Nicholas Henderson
article en
7 citations

Abstract

Patients with <i>BRCA1/2</i>-mutated PC had significantly improved outcomes to PARPi but not platinum chemotherapy compared with those with HRR mutations without direct BRCA complex interaction.

JCO Precision OncologyVol. 8(8)
Baptist Hospital of Miami (US), Emory University (US), University of California, San Francisco (US), Wayne State University (US), University of Washington (US), Medical College of Wisconsin (US), University of Michigan (US), Henry Ford Hospital (US), University of California San Diego (US), Fred Hutch Cancer Center (US), The Barbara Ann Karmanos Cancer Institute (US), Baptist Health South Florida (US), City of Hope (US), University Hospitals Seidman Cancer Center (US), Duke Medical Center (US), Oklahoma State University Oklahoma City (US), UCSF Helen Diller Family Comprehensive Cancer Center (US), OU Health Stephenson Cancer Center, University of Colorado Anschutz Medical Campus (US), University of Colorado Denver (US), Icahn School of Medicine at Mount Sinai (US)
Bristol-Myers Squibb, Pfizer, AstraZeneca, Sanofi, Genomic Health, Endocyte, Exelixis, Incyte, Calithera Biosciences, Seagen, Eisai, Astellas Pharma, Genentech, EMD Serono
Good health and well-being
Openalex Percentile: Top 11%
PARP inhibition in cancer therapy
1.98
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