| Literature DB >> 34409858 |
David M O'Malley1, Leslie M Randall2, Camille Gunderson Jackson3, Robert L Coleman4, John L Hays1, Kathleen N Moore3, R Wendel Naumann5, Rodney P Rocconi6, Brian M Slomovitz7, Krishnansu S Tewari8, Marek Ancukiewicz9, Waldo Ortuzar Feliu9, Bradley J Monk10.
Abstract
Balstilimab (anti-programmed death 1) and zalifrelimab (anti-CTLA-4) are two new checkpoint inhibitors that have emerged as promising investigational agents for the treatment of cervical cancer, particularly in the setting of previously-treated, recurrent/metastatic disease. Here we describe the rationale and design of RaPiDS (NCT03894215), a two-arm Phase II study evaluating the safety, tolerability and efficacy of balstilimab administered alone or in combination with zalifrelimab in patients with advanced cervical cancer who progressed after first-line, platinum-based chemotherapy. Patients will be randomized in a 1:1 ratio. The primary end point is objective response rate, and key secondary objectives include safety, duration of response, progression-free survival, overall survival and quality of life outcomes.Entities:
Keywords: CTLA-4; PD-1; balstilimab; cervical cancer; immuno-oncology; zalifrelimab
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Year: 2021 PMID: 34409858 DOI: 10.2217/fon-2021-0529
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404