Back to Search
Start Over
Pembrolizumab plus either epacadostat or placebo for cisplatin-ineligible urothelial carcinoma:results from the ECHO-307/KEYNOTE-672 study
- Source :
- Necchi , A , Van der Heijden , M S , Trukhin , D , Peer , A , Gurney , H , Alekseev , B Y , Parnis , F X , Leibowitz , R , De Santis , M , Grivas , P , Clark , J , Munteanu , M , Kataria , R , Jia , C , Balar , A V & de Wit , R 2024 , ' Pembrolizumab plus either epacadostat or placebo for cisplatin-ineligible urothelial carcinoma : results from the ECHO-307/KEYNOTE-672 study ' , BMC Cancer , vol. 23 , no. Suppl 1 , 1252 .
- Publication Year :
- 2024
-
Abstract
- Background: Indoleamine 2,3- dioxygenase 1 (IDO1) is an immunosuppressive enzyme that has been correlated with shorter disease-specific survival in patients with urothelial carcinoma (UC). IDO1 may counteract the antitumor effects of immune checkpoint inhibitors. Epacadostat is a potent and highly selective inhibitor of IDO1. In the phase I/II ECHO-202/KEYNOTE-037 study, epacadostat plus pembrolizumab resulted in a preliminary objective response rate (ORR) of 35% in a cohort of patients with advanced UC. Methods: ECHO-307/KEYNOTE-672 was a double-blinded, randomized, phase III study. Eligible adults had confirmed locally advanced/unresectable or metastatic UC of the urinary tract and were ineligible to receive cisplatin-based chemotherapy. Participants were randomly assigned (1:1) to receive epacadostat (100 mg twice daily) plus pembrolizumab (200 mg every 3 weeks) or placebo plus pembrolizumab for up to 35 pembrolizumab infusions. The primary endpoint was investigator-assessed ORR per Response Evaluation Criteria in Solid Tumors (version 1.1). Results: A total of 93 patients were randomized (epacadostat plus pembrolizumab, n = 44; placebo plus pembrolizumab, n = 49). Enrollment was stopped early due to emerging data from the phase III ECHO-301/KEYNOTE-252 study. The median duration of follow-up was 64 days in both arms. Based on all available data at cutoff, ORR (unconfirmed) was 31.8% (95% CI, 22.46–55.24%) for epacadostat plus pembrolizumab and 24.5% (95% CI, 15.33–43.67%) for placebo plus pembrolizumab. Circulating kynurenine levels numerically increased from C1D1 to C2D1 in the placebo-plus-pembrolizumab arm and decreased in the epacadostat-plus-pembrolizumab arm. Epacadostat-plus-pembrolizumab combination treatment was well tolerated with a safety profile similar to the placebo arm. Treatment discontinuations due to treatment-related adverse events were more frequent with epacadostat (11.6% vs. 4.1%). Conclusions: Treatment with epacadostat plus pembrolizum
Details
- Database :
- OAIster
- Journal :
- Necchi , A , Van der Heijden , M S , Trukhin , D , Peer , A , Gurney , H , Alekseev , B Y , Parnis , F X , Leibowitz , R , De Santis , M , Grivas , P , Clark , J , Munteanu , M , Kataria , R , Jia , C , Balar , A V & de Wit , R 2024 , ' Pembrolizumab plus either epacadostat or placebo for cisplatin-ineligible urothelial carcinoma : results from the ECHO-307/KEYNOTE-672 study ' , BMC Cancer , vol. 23 , no. Suppl 1 , 1252 .
- Notes :
- application/pdf, English
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.on1452811603
- Document Type :
- Electronic Resource