Phase II Trial of the PARP Inhibitor, Niraparib, in BAP1 and Other DNA Damage Response Pathway-Deficient Neoplasms

Niraparib failed to meet the prespecified efficacy end point for response. However, clinical benefit was suggested in a proportion of patients who had a confirmed mBAP1, supporting further investigation.

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Institutions

Publication Details

Journal
JCO Precision Oncology
Published
2024-12-01
DOI
https://doi.org/10.1200/po-24-00406
Citations
11
Primary Topic
PARP inhibition in cancer therapy
Type
article
Field-Weighted Citation Impact
3.11

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article

Phase II Trial of the PARP Inhibitor, Niraparib, in BAP1 and Other DNA Damage Response Pathway-Deficient Neoplasms

Gayathri Srinivasan, Julia Close, Nkiruka Ezenwajiaku, Thomas J. George et al.
11 citations
JCO Precision Oncology
PARP inhibition in cancer therapy
3.11
article

Phase II Trial of the PARP Inhibitor, Niraparib, in BAP1 and Other DNA Damage Response Pathway-Deficient Neoplasms

Gayathri Srinivasan, Julia Close, Nkiruka Ezenwajiaku, Thomas J. George, Merry Jennifer Markham, Robert Hromas, Dennie V. Jones, Karen Daily, Steven Staal, Sherise C. Rogers, Martina Murphy, David L. DeRemer, Brian Hemendra Ramnaraign, Peter J. Hosein, Carmen J. Allegra, Derek Li, Jonathan Alexander Chatzkel, Montaser Shaheen, Ji‐Hyun Lee, Zhongyue Zhang
article en
11 citations

Abstract

Niraparib failed to meet the prespecified efficacy end point for response. However, clinical benefit was suggested in a proportion of patients who had a confirmed mBAP1, supporting further investigation.

JCO Precision OncologyVol. 8(8)
University of Miami (US), University of Florida Health (US), University of Florida (US), Sylvester Comprehensive Cancer Center (US), UF Health Cancer Center, The University of Texas at San Antonio (US)
Eli Lilly and Company, Pfizer, AstraZeneca, GlaxoSmithKline, FibroGen, Florida Department of Health, Florida Breast Cancer Foundation, Genentech, University of Florida Health, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 7%
PARP inhibition in cancer therapy
3.11
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