Olaparib treatment for platinum-sensitive relapsed ovarian cancer by BRCA mutation and homologous recombination deficiency status: Phase II LIGHT study primary analysis.


Journal

Gynecologic oncology
ISSN: 1095-6859
Titre abrégé: Gynecol Oncol
Pays: United States
ID NLM: 0365304

Informations de publication

Date de publication:
09 2022
Historique:
received: 16 05 2022
accepted: 20 06 2022
pubmed: 9 7 2022
medline: 15 9 2022
entrez: 8 7 2022
Statut: ppublish

Résumé

Olaparib treatment resulted in significant improvement in objective response rates (ORRs) and progression-free survival (PFS) over non‑platinum chemotherapy in patients with BRCA1/BRCA2-mutated (BRCAm) platinum-sensitive relapsed ovarian cancer (PSROC) and ≥2 prior lines of platinum-based chemotherapy in the phase III SOLO3 study. LIGHT (NCT02983799) prospectively evaluated olaparib treatment for patients with PSROC and known BRCAm and homologous recombination deficiency (HRD) status. In this phase II open-label multicenter study, patients with PSROC and ≥1 prior line of platinum-based chemotherapy were assigned to cohorts by presence of germline BRCAm (gBRCAm), somatic BRCAm (sBRCAm), HRD-positive tumors without BRCAm, or HRD-negative tumors. The primary endpoint was investigator-assessed ORR. Secondary endpoints included disease control rate (DCR) and PFS. Tumors were analyzed using Myriad BRACAnalysis CDx and myChoice HRD assays; HRD-positive tumors were defined using a genomic instability score of ≥42. Of 272 enrolled patients, 271 received olaparib and 270 were included in efficacy analyses. At data cut-off, ORRs in the gBRCAm, sBRCAm, HRD-positive, and HRD-negative cohorts were 69.3%, 64.0%, 29.4%, and 10.1%, respectively. DCRs were 96.0%, 100.0%, 79.4%, and 75.3% in each cohort, respectively. Median PFS was 11.0, 10.8, 7.2, and 5.4 months, respectively. The most common (≥ 20%) treatment-emergent adverse events included nausea, fatigue/asthenia, vomiting, anemia, constipation, diarrhea, and decreased appetite. Olaparib treatment demonstrated activity across all cohorts. The greatest efficacy was observed in the BRCAm cohorts, regardless of gBRCAm/sBRCAm. For patients without a BRCAm, greater efficacy was observed in the HRD-positive than the HRD-negative cohorts. The safety profile was consistent with that established in previous olaparib studies.

Identifiants

pubmed: 35803835
pii: S0090-8258(22)00421-8
doi: 10.1016/j.ygyno.2022.06.017
pmc: PMC9909678
mid: NIHMS1868098
pii:
doi:

Substances chimiques

BRCA1 Protein 0
BRCA2 Protein 0
Phthalazines 0
Piperazines 0
olaparib WOH1JD9AR8

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

425-431

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

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Auteurs

Karen Cadoo (K)

Memorial Sloan Kettering Cancer Center, and Weill Cornell Medical College, New York, NY, USA,. Electronic address: kcadoo@stjames.ie.

Fiona Simpkins (F)

Department of Obstetrics and Gynecology, Jordan Center for Gynecologic Oncology at the Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA, USA.

Cara Mathews (C)

Program in Women's Oncology, Department of Obstetrics and Gynecology, Women and Infants Hospital, Brown University, Providence, RI, USA.

Ying L Liu (YL)

Memorial Sloan Kettering Cancer Center, and Weill Cornell Medical College, New York, NY, USA.

Diane Provencher (D)

CHUM Gynecologie-Oncologie, Montreal, QC, Canada.

Colleen McCormick (C)

Legacy Medical Group Gynecologic Oncology, Portland, OR, USA.

Adam C ElNaggar (AC)

West Cancer Center and Research Institute, Memphis, TN, USA.

Alon D Altman (AD)

CancerCare Manitoba, Research Institute of Oncology and Hematology, University of Manitoba, Winnipeg, Manitoba, Canada.

Lucy Gilbert (L)

Division of Gynecologic Oncology, McGill University Health Centre, Montreal, Quebec, Canada.

Destin Black (D)

Willis-Knighton Cancer Center, Shreveport, LA, USA.

Nashwa Kabil (N)

AstraZeneca, Gaithersburg, MD, USA.

James Bennett (J)

AstraZeneca, Cambridge, UK.

Jiefen Munley (J)

AstraZeneca, Wilmington, DE, USA.

Carol Aghajanian (C)

Memorial Sloan Kettering Cancer Center, and Weill Cornell Medical College, New York, NY, USA.

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Classifications MeSH