Author:
Schouten Philip C.,Schmidt Sandra,Becker Kerstin,Thiele Holger,Nürnberg Peter,Richters Lisa,Ernst Corinna,Treilleux Isabelle,Medioni Jacques,Heitz Florian,Pisano Carmela,Garcia Yolanda,Petru Edgar,Hietanen Sakari,Colombo Nicoletta,Vergote Ignace,Nagao Shoji,Linn Sabine C.,Pujade Lauraine Eric,Ray-Coquard Isabelle,Harter Philip,Hahnen Eric,Schmutzler Rita K.
Abstract
AbstractBackgroundWe previously established an ovarian carcinoma (OC)BRCA-like genomic copy number aberration profile classifier (“BRCA-like classifier”), which identifies tumors with deleterious mutations and epigenetic alterations in the homologous recombination pathway (1). We explored whether the classifier may also be predictive for therapies targeting tumors with homologous recombination deficiency (HRD) such as olaparib, a PARP inhibitor with synthetic lethal interaction with HRD, in combination with bevacizumab.MethodsAs part of the ENGOT (European Network of Gynaecological Oncological Trial groups) HRD initiative, the OCBRCA-like classifier was evaluated using tumor-derived DNA samples from 469 out of 806 patients enrolled in the PAOLA-1/ENGOT-ov25 trial. PAOLA-1 is a randomized, double-blind, international phase 3 trial (NCT02477644) including advanced high grade OC patients. Prolonged progression-free survival (PFS) and overall survival (OS) was observed for patients treated with maintenance olaparib and bevacizumab versus placebo and bevacizumab, and particularly for those patients tested HRD positive according to Myriad MyChoice® CDx HRD test.ResultsResults were obtained for 442 patients (failure rate of 6%, 27 of 469 samples). A survival benefit from adding maintenance olaparib was observed in the 298 (67%) patients with aBRCA-like tumor (hazard ratio (HR) for PFS: 0.49, 95% confidence interval (CI) 0.37-0.65, p = 0.01; OS: 0.64, 95% CI 0.45-0.90, p < 0.01). No benefit was detected in patients with a non-BRCA-like tumor when treated with olaparib (HR for PFS: 1.02, 95% CI 0.68-1.51, p = 0.93; OS 1.48, 95% CI 0.94-2.33, p = 0.09). P values for interaction betweenBRCA-like status and olaparib for PFS and OS were both 0.004. Multivariate analysis revealed comparable results. The concordance rate with the Myriad test was 77% in samples that were successfully analysed with both assays. In the survival analyses, the CIs of theBRCA-like classifier and the Myriad test overlap.ConclusionTheBRCA-like classifier is a high-sensitive predictive biomarker for survival benefit of olaparib/bevacizumab as maintenance therapy in advanced ovarian carcinoma with a low drop-out rate.
Publisher
Cold Spring Harbor Laboratory