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Pembrolizumab plus either epacadostat or placebo for cisplatin-ineligible urothelial carcinoma:results from the ECHO-307/KEYNOTE-672 study

Authors :
Necchi, Andrea
Van der Heijden, Michiel S.
Trukhin, Dmytro
Peer, Avivit
Gurney, Howard
Alekseev, Boris Y.
Parnis, Francis X.
Leibowitz, Raya
De Santis, Maria
Grivas, Petros
Clark, Jason
Munteanu, Mihaela
Kataria, Ritesh
Jia, Calvin
Balar, Arjun V.
de Wit, Ronald
Necchi, Andrea
Van der Heijden, Michiel S.
Trukhin, Dmytro
Peer, Avivit
Gurney, Howard
Alekseev, Boris Y.
Parnis, Francis X.
Leibowitz, Raya
De Santis, Maria
Grivas, Petros
Clark, Jason
Munteanu, Mihaela
Kataria, Ritesh
Jia, Calvin
Balar, Arjun V.
de Wit, Ronald
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