Author:
Murakami Ryusuke,Hamanishi Junzo,Brown J. B.,Abiko Kaoru,Yamanoi Koji,Taki Mana,Hosoe Yuko,Yamaguchi Ken,Baba Tsukasa,Matsumura Noriomi,Konishi Ikuo,Mandai Masaki
Abstract
AbstractBased on our previous phase II clinical trial of anti-programmed death-1 (PD-1) antibody nivolumab for platinum-resistant ovarian cancer (n = 19, UMIN000005714), we aimed to identify the biomarkers predictive of response. Tumor gene expression was evaluated by proliferative, mesenchymal, differentiated, and immunoreactive gene signatures derived from high-grade serous carcinomas and a signature established prior for ovarian clear cell carcinoma. Resulting signature scores were statistically assessed with both univariate and multivariate approaches for correlation to clinical response. Analyses were performed to identify pathways differentially expressed by either the complete response (CR) or progressive disease (PD) patient groups. The clear cell gene signature was scored significantly higher in the CR group, and the proliferative gene signature had significantly higher scores in the PD group where nivolumab was not effective (respective p values 0.005 and 0.026). Combinations of gene signatures improved correlation with response, where a visual projection of immunoreactive, proliferative, and clear cell signatures differentiated clinical response. An applicable clinical response prediction formula was derived. Ovarian cancer-specific gene signatures and related pathway scores provide a robust preliminary indicator for ovarian cancer patients prior to anti-PD-1 therapy decisions.
Funder
the Japanese Society for the Promotion of Science
the Project for Development of Innovative Research on Cancer Therapeutics of the Japan Agency for Medical Research and Development grant
Publisher
Springer Science and Business Media LLC
Cited by
3 articles.
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