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  4. Antitumor activity of pembrolizumab in biomarker-unselected patients with recurrent and/or metastatic head and neck squamous cell carcinoma: Results from the phase Ib KEYNOTE-012 expansion cohort
 
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Antitumor activity of pembrolizumab in biomarker-unselected patients with recurrent and/or metastatic head and neck squamous cell carcinoma: Results from the phase Ib KEYNOTE-012 expansion cohort

Journal
Journal of Clinical Oncology
Journal Volume
34
Journal Issue
32
Pages
3838-3845
Date Issued
2016
Author(s)
Chow L.Q.M.
Haddad R.
Gupta S.
Mahipal A.
Mehra R.
Tahara M.
Berger R.
Eder J.P.
Burtness B.
Lee S.-H.
Keam B.
Kang H.
Muro K.
Weiss J.
Geva R.
CHIA-CHI LIN  
Chung H.C.
Meister A.
Dolled-Filhart M.
Pathiraja K.
Cheng J.D.
Seiwert T.Y.
DOI
10.1200/JCO.2016.68.1478
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84995489253&doi=10.1200%2fJCO.2016.68.1478&partnerID=40&md5=31ab6170cee8cf13626ef51bb5e4484d
https://scholars.lib.ntu.edu.tw/handle/123456789/620289
Abstract
Purpose Treatment with pembrolizumab, an anti-programmed death-1 antibody, at 10 mg/kg administered once every 2 weeks, displayed durable antitumor activity in programmed death-ligand 1 (PD-L1) -positive recurrent and/or metastatic (R/M) head and neck squamous cell carcinoma (HNSCC) in the KEYNOTE-012 trial. Results from the expansion cohort, in which patients with HNSCC, irrespective of biomarker status, received a fixed dose of pembrolizumab at a less frequent dosing schedule, are reported. Patients and Methods Patients with R/M HNSCC, irrespective of PD-L1 or human papillomavirus status, received pembrolizumab 200 mg intravenously once every 3 weeks. Imaging was performed every 8 weeks. Primary end points were overall response rate (ORR) per central imaging vendor (Response Evaluation Criteria in Solid Tumors v1.1) and safety. Secondary end points included progression-free survival, overall survival, and association of response and PD-L1 expression. Patients who received one or more doses of pembrolizumab were included in analyses. Results Of 132 patients enrolled, median age was 60 years (range, 25 to 84 years), 83% were male, and 57% received two or more lines of therapy for R/M disease. ORR was 18% (95% CI, 12 to 26) by central imaging vendor and 20% (95% CI, 13 to 28) by investigator review. Median duration of response was not reached (range, ≥ 2 to ≥ 11 months). Six-month progression-free survival and overall survival rates were 23% and 59%, respectively. By using tumor and immune cells, a statistically significant increase in ORR was observed for PD-L1-positive versus -negative patients (22% v 4%; P = .021). Treatment-related adverse events of any grade and grade ≥ 3 events occurred in 62% and 9% of patients, respectively. Conclusion Fixed-dose pembrolizumab 200 mg administered once every 3 weeks was well tolerated and yielded a clinically meaningful ORR with evidence of durable responses, which supports further development of this regimen in patients with advanced HNSCC.
SDGs

[SDGs]SDG3

Publisher
American Society of Clinical Oncology
Type
journal article

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