Literature DB >> 32359091

Efficacy and safety of pembrolizumab for the treatment of advanced biliary cancer: Results from the KEYNOTE-158 and KEYNOTE-028 studies.

Sarina A Piha-Paul1, Do-Youn Oh2, Makoto Ueno3, David Malka4, Hyun Cheol Chung5, Adnan Nagrial6, Robin K Kelley7, Willeke Ros8, Antoine Italiano9, Kazuhiko Nakagawa10, Hope S Rugo11, Filippo de Braud12, Andrea Iolanda Varga13, Aaron Hansen14, Hui Wang15, Suba Krishnan16, Kevin G Norwood16, Toshihiko Doi17.   

Abstract

We present data from patients with advanced biliary tract cancer (BTC) receiving pembrolizumab in the KEYNOTE-158 (NCT02628067; phase 2) and KEYNOTE-028 (NCT02054806; phase 1b) studies. Eligible patients aged ≥18 years from both studies had histologically/cytologically confirmed incurable BTC that progressed after standard treatment regimen(s), measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1, Eastern Cooperative Oncology Group performance status 0/1, and no prior immunotherapy. Programmed death ligand 1 (PD-L1)-positive tumors were required for eligibility in KEYNOTE-028 only. Patients received pembrolizumab 200 mg every three weeks (KEYNOTE-158) or 10 mg/kg every two weeks (KEYNOTE-028) for ≤2 years. Primary efficacy endpoint was objective response rate (ORR) by RECIST v1.1. Response assessed by independent central review is reported. KEYNOTE-158 enrolled 104 patients and KEYNOTE-028 enrolled 24 patients. Median (range) follow-up was 7.5 months (0.6-34.3) in KEYNOTE-158 and 5.7 months (0.6-55.4) in KEYNOTE-028. In KEYNOTE-158, ORR was 5.8% (6/104; 95% CI, 2.1%-12.1%); median duration of response (DOR) was not reached (NR) (range, 6.2-26.6+ months). Median (95% CI) OS and PFS were 7.4 (5.5-9.6) and 2.0 (1.9-2.1) months. Among PD-L1-expressers (n = 61) and PD-L1-nonexpressers (n = 34), respectively, ORR was 6.6% (4/61) and 2.9% (1/34). In KEYNOTE-028, ORR was 13.0% (3/23; 95% CI, 2.8%-33.6%); median DOR was NR (range, 21.5-53.2+ months). Median (95% CI) OS and PFS were 5.7 (3.1-9.8) and 1.8 (1.4-3.1) months. Grade 3 to 5 treatment-related adverse events occurred in 13.5% of patients in KEYNOTE-158 (no grade 4; grade 5 renal failure, n = 1) and 16.7% in KEYNOTE-028 (no grade 4/5). In summary, pembrolizumab provides durable antitumor activity in 6% to 13% of patients with advanced BTC, regardless of PD-L1 expression, and has manageable toxicity.
© 2020 UICC.

Entities:  

Keywords:  MSI-H; PD-L1; biliary tract cancer; pembrolizumab

Mesh:

Substances:

Year:  2020        PMID: 32359091     DOI: 10.1002/ijc.33013

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  75 in total

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Review 4.  Targeting the tumor microenvironment in cholangiocarcinoma: implications for therapy.

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Review 9.  Biomarkers in Hepatobiliary Cancers: What is Useful in Clinical Practice?

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10.  PD-1 Inhibitors Could Improve the Efficacy of Chemotherapy as First-Line Treatment in Biliary Tract Cancers: A Propensity Score Matching Based Analysis.

Authors:  Miaomiao Gou; Yong Zhang; Tiee Liu; Haiyan Si; Zhikuan Wang; Huan Yan; Niansong Qian; Guanghai Dai
Journal:  Front Oncol       Date:  2021-06-17       Impact factor: 6.244

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