Maintenance olaparib monotherapy in patients with platinum-sensitive relapsed ovarian cancer without a germline BRCA1 and/or BRCA2 mutation: Final overall survival results from the OPINION trial
Language English Country United States Media print-electronic
Document type Journal Article, Clinical Trial, Phase III, Multicenter Study
PubMed
40300425
DOI
10.1016/j.ygyno.2025.04.580
PII: S0090-8258(25)00806-6
Knihovny.cz E-resources
- Keywords
- BRCA, Maintenance, Olaparib, Ovarian cancer,
- MeSH
- Progression-Free Survival MeSH
- Adult MeSH
- Carcinoma, Ovarian Epithelial * drug therapy genetics mortality MeSH
- Phthalazines * adverse effects administration & dosage therapeutic use MeSH
- Middle Aged MeSH
- Humans MeSH
- Neoplasm Recurrence, Local * drug therapy genetics MeSH
- Ovarian Neoplasms * drug therapy genetics mortality MeSH
- Poly(ADP-ribose) Polymerase Inhibitors * adverse effects administration & dosage therapeutic use MeSH
- Piperazines * adverse effects administration & dosage therapeutic use MeSH
- BRCA1 Protein genetics MeSH
- BRCA2 Protein genetics MeSH
- Aged MeSH
- Maintenance Chemotherapy MeSH
- Germ-Line Mutation MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial, Phase III MeSH
- Multicenter Study MeSH
- Names of Substances
- BRCA1 protein, human MeSH Browser
- BRCA2 protein, human MeSH Browser
- Phthalazines * MeSH
- olaparib MeSH Browser
- Poly(ADP-ribose) Polymerase Inhibitors * MeSH
- Piperazines * MeSH
- BRCA1 Protein MeSH
- BRCA2 Protein MeSH
OBJECTIVE: Maintenance olaparib demonstrated clinical activity for progression-free survival in patients without a germline BRCA1 and/or BRCA2 mutation (non-gBRCAm) who had platinum-sensitive relapsed ovarian cancer in the phase IIIb, open-label, single-arm, non-comparator, international OPINION trial (NCT03402841). We report final overall survival (OS; secondary endpoint), prespecified secondary endpoint updates and ad hoc OS analysis by homologous recombination deficiency (HRD) and somatic BRCAm (sBRCAm) status. METHODS: Patients with non-gBRCAm platinum-sensitive relapsed ovarian cancer, ≥2 prior lines of platinum-based chemotherapy, and in response following their last platinum-based chemotherapy received 300 mg olaparib tablets twice daily until disease progression or unacceptable toxicity. RESULTS: 279 patients were enrolled and treated. With a median follow-up in patients censored for OS of 33.1 months (data cut-off September 17, 2021), median OS was 32.7 months (95 % CI 29.5-35.3); the 24-month OS rate was 65.8 %. In ad hoc subgroup analyses, OS rates tended to be higher in patients with HRD-positive tumors; 24-month OS rates were 81.5 %, 74.2 %, 72.0 % and 55.8 % in the sBRCAm, HRD-positive including sBRCAm, HRD-positive excluding sBRCAm, and HRD-negative subgroups, respectively. Grade ≥ 3 treatment-emergent adverse events were reported in 82 patients (29.4 %), most commonly anemia (13.6 %). Overall, two cases of myelodysplastic syndrome were reported (no new cases since the primary analysis). CONCLUSION: These data provide additional evidence of olaparib as maintenance therapy in patients with non-gBRCAm platinum-sensitive relapsed ovarian cancer, with longer OS observed in those with HRD-positive tumors. The safety profile was consistent with the primary analysis and known safety profile of olaparib, with no new safety findings.
Cancer Center Clinica Universidad de Navarra Madrid Spain; CIMA Pamplona Spain
General University Hospital Prague 1st Faculty of Medicine Charles University Prague Czech Republic
Hospital Universitario Reina Sofía Córdoba Spain
Initia Oncology Valencia Spain
Institute of Oncology Ljubljana Ljubljana Slovenia
Medical University Karol Marcinkowski Poznań Poland
Olsztyn Provincial Specialist Hospital Olsztyn Poland
Oncology R and D AstraZeneca Cambridge UK
Oslo University Hospital Norwegian Radium Hospital Oslo Norway
Ottawa Hospital Research Institute Ottawa ON Canada
Princess Margaret Hospital Toronto ON Canada
Skåne University Hospital Lund University Lund Sweden
UCL Cancer Institute University College London and UCL Hospitals London UK
University of Milan Bicocca and European Institute of Oncology IRCCS Milan Italy
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