| Literature DB >> 31416802 |
Anna F Farago1,2, Beow Y Yeap3,2, Marcello Stanzione3, Yin P Hung3,2, Rebecca S Heist3,2, J Paul Marcoux2,4, Jun Zhong3, Deepa Rangachari2,5, David A Barbie2,4, Sarah Phat3, David T Myers3, Robert Morris3, Marina Kem3, Taronish D Dubash3, Elizabeth A Kennedy3, Subba R Digumarthy2,6, Lecia V Sequist3,2, Aaron N Hata3,2, Shyamala Maheswaran3,2, Daniel A Haber3,2,7, Michael S Lawrence3,2, Alice T Shaw3,2, Mari Mino-Kenudson3,2, Nicholas J Dyson3,2, Benjamin J Drapkin1,2.
Abstract
Small-cell lung cancer (SCLC) is an aggressive malignancy in which inhibitors of PARP have modest single-agent activity. We performed a phase I/II trial of combination olaparib tablets and temozolomide (OT) in patients with previously treated SCLC. We established a recommended phase II dose of olaparib 200 mg orally twice daily with temozolomide 75 mg/m2 daily, both on days 1 to 7 of a 21-day cycle, and expanded to a total of 50 patients. The confirmed overall response rate was 41.7% (20/48 evaluable); median progression-free survival was 4.2 months [95% confidence interval (CI), 2.8-5.7]; and median overall survival was 8.5 months (95% CI, 5.1-11.3). Patient-derived xenografts (PDX) from trial patients recapitulated clinical OT responses, enabling a 32-PDX coclinical trial. This revealed a correlation between low basal expression of inflammatory-response genes and cross-resistance to both OT and standard first-line chemotherapy (etoposide/platinum). These results demonstrate a promising new therapeutic strategy in SCLC and uncover a molecular signature of those tumors most likely to respond. SIGNIFICANCE: We demonstrate substantial clinical activity of combination olaparib/temozolomide in relapsed SCLC, revealing a promising new therapeutic strategy for this highly recalcitrant malignancy. Through an integrated coclinical trial in PDXs, we then identify a molecular signature predictive of response to OT, and describe the common molecular features of cross-resistant SCLC.See related commentary by Pacheco and Byers, p. 1340.This article is highlighted in the In This Issue feature, p. 1325. ©2019 American Association for Cancer Research.Entities:
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Year: 2019 PMID: 31416802 PMCID: PMC7319046 DOI: 10.1158/2159-8290.CD-19-0582
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397