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Poly(ADP)-Ribose Polymerase Inhibition: Frequent Durable Responses in BRCA Carrier Ovarian Cancer Correlating With Platinum-Free Interval
- Publication Year :
- 2010
- Publisher :
- American Society of Clinical Oncology, 2010.
-
Abstract
- Purpose Selective tumor cell cytotoxicity can be achieved through a synthetic lethal strategy using poly(ADP)-ribose polymerase (PARP) inhibitor therapy in BRCA1/2 mutation carriers in whom tumor cells have defective homologous recombination (HR) DNA repair. Platinum-based chemotherapy responses correlate with HR DNA repair capacity. Olaparib is a potent, oral PARP inhibitor that is well tolerated, with antitumor activity in BRCA1/2 mutation carriers. Patients and Methods Patients with BRCA1/2-mutated ovarian cancer were treated with olaparib within a dose-escalation and single-stage expansion of a phase I trial. Antitumor activity was subsequently correlated with platinum sensitivity. Results Fifty patients were treated: 48 had germline BRCA1/2 mutations; one had a BRCA2 germline sequence change of unknown significance, and another had a strong family history of BRCA1/2-associated cancers who declined mutation testing. Of the 50 patients, 13 had platinum-sensitive disease, 24 had platinum-resistant disease, and 13 had platinum-refractory disease (according to platinum-free interval). Twenty (40%; 95% CI, 26% to 55%) achieved Response Evaluation Criteria in Solid Tumors (RECIST) complete or partial responses and/or tumor marker (CA125) responses, and three (6.0%) maintained RECIST disease stabilization for more than 4 months, giving an overall clinical benefit rate of 46% (95% CI, 32% to 61%). Median response duration was 28 weeks. There was a significant association between the clinical benefit rate and platinum-free interval across the platinum-sensitive, resistant, and refractory subgroups (69%, 45%, and 23%, respectively). Post hoc analyses indicated associations between platinum sensitivity and extent of olaparib response (radiologic change, P = .001; CA125 change, P = .002). Conclusion Olaparib has antitumor activity in BRCA1/2 mutation ovarian cancer, which is associated with platinum sensitivity.
- Subjects :
- Oncology
Cancer Research
PTEN
endocrine system diseases
Genes, BRCA2
Genes, BRCA1
Poly (ADP-Ribose) Polymerase Inhibitor
Piperazines
Cohort Studies
chemistry.chemical_compound
Peritoneal Neoplasms
Aged, 80 and over
Ovarian Neoplasms
Middle Aged
SOLID TUMORS
female genital diseases and pregnancy complications
POLY POLYMERASE
Response Evaluation Criteria in Solid Tumors
CHEMOTHERPAY
PARP inhibitor
Female
Poly(ADP-ribose) Polymerases
Mutations
Adult
medicine.medical_specialty
Poly(ADP-ribose) Polymerase Inhibitors
Olaparib
resistance
Germline mutation
Cell Line, Tumor
Internal medicine
medicine
Fallopian Tube Neoplasms
Humans
Rucaparib
Germ-Line Mutation
breast
Aged
Neoplasm Staging
Tumor marker
REPAIR
Dose-Response Relationship, Drug
MUTANT-CELLS
business.industry
medicine.disease
HYPERMETHYLATION
chemistry
Drug Resistance, Neoplasm
Pharmacogenetics
Immunology
Phthalazines
business
Ovarian cancer
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....6fc817aad57a3be44547bce41ce9ccba