Pembrolizumab (pembro) for recurrent head and neck squamous cell carcinoma (HNSCC): Post hoc analyses of phase 3 KEYNOTE-040 prior radiation treatment (RT) and disease state.

Authors

null

Kevin J. Harrington

The Institute of Cancer Research/The Royal Marsden NHS Foundation Trust National Institute of Health Research Biomedical Research Centre, London, United Kingdom

Kevin J. Harrington , Ezra E.W. Cohen , Denis Soulieres , José Dinis , Lisa F. Licitra , Myung-Ju Ahn , Ainara Soria , Jean-Pascal H. Machiels , Nicolas Mach , Ranee Mehra , Barbara Burtness , Jianxin Lin , Jonathan D. Cheng , Ramona F. Swaby , Christophe Le Tourneau

Organizations

The Institute of Cancer Research/The Royal Marsden NHS Foundation Trust National Institute of Health Research Biomedical Research Centre, London, United Kingdom, Moores Cancer Center, UC San Diego Health, La Jolla, CA, Centre Hospitalier de l'Université de Montréal, Montreal, QC, Canada, Instituto Português de Oncologia do Porto Francisco Gentil, Porto, Portugal, Fondazione IRCCS Istituto Nazionale dei Tumori and University of Milan, Milan, Italy, Samsung Medical Center, Seoul, South Korea, Hospital Universitario Ramón y Cajal, Madrid, Spain, Cliniques Universitaires Saint-Luc, Brussels, Belgium, Hôpitaux Universitaires de Genève, Geneva, Switzerland, Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, Yale University School of Medicine and Yale Cancer Center, New Haven, CT, Merck & Co., Inc., Kenilworth, NJ, Institut Curie, Paris & Saint-Cloud, INSERM U900 Research Unit, Saint-Cloud, France

Research Funding

Pharmaceutical/Biotech Company

Background: The open-label, randomized, phase 3 KEYNOTE-040 study (NCT02252042) showed that pembro vs standard of care (SOC) chemotherapy prolonged survival in patients (pts) with recurrent and/or metastatic HNSCC whose disease progressed during/after platinum-based therapy. Post hoc analyses were conducted to evaluate pembro vs SOC by prior RT and disease state (metastatic, locoregionally recurrent [referred to as recurrent herein], or recurrent and metastatic [R/M]). Methods: Pts (N = 495) were randomly assigned (1:1) to receive pembro (200 mg Q3W) or investigator choice of methotrexate (40 mg/m2 QW), docetaxel (75 mg/m2 Q3W), or cetuximab (400 mg/m2 loading dose, then 250 mg/m2 QW). Primary end point was OS; PFS and ORR were secondary end points. Results: 175, 97, and 195 pts had metastatic, recurrent, and R/M disease, respectively (28 pts had unknown disease state); 64 pts had no prior RT; 431 pts had prior RT. As in the ITT population, prolonged survival benefit and trend toward improved PFS and ORR was observed with pembro vs SOC in pts with prior RT (Table), and prolonged survival benefit was observed with pembro vs SOC in pts with metastatic and R/M, but not recurrent, disease. Conclusions: In this post hoc analysis, patients with prior RT benefited from treatment with pembro vs SOC. For patients without RT, sample sizes are too small to draw any definitive conclusions. Survival benefit of pembro vs SOC was observed in pts with metastatic and R/M disease. Clinical trial information: NCT02252042

Metastatic Pembro
n = 90
Metastatic SOC
n = 85
Recurrent Pembro
n = 43
Recurrent SOC
n = 54
R/M Pembro
n = 104
R/M SOC
n = 91
OS: Median, mo8.97.97.29.16.75.6
OS: pembro vs SOC0.721.070.79
HR(0.52-1.03)(0.67-1.69)(0.58-1.07)
(95% CI)0.0380.6070.065
P
Prior RTPrior RTNo Prior RTNo Prior RT
PembroSOCPembroSOC
n = 217n = 214n = 30n = 34
OS: Median, mo8.46.67.29.4
OS: pembro vs SOC0.751.01
HR(0.60-0.93)(0.59-1.74)
(95% CI)0.0040.520
P2.12.22.13.9
PFS: Median, mo
PFS: pembro vs SOC0.871.32
HR(0.71-1.07)(0.80-2.18)
(95% CI)0.0860.854
P15.711.26.72.9
ORR: %
ORR: pembro vs SOC4.53.7
Difference(−2.0-11.0)(−9.3-19.0)
(95% CI)0.0880.243
P

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Abstract Details

Meeting

2019 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Head and Neck Cancer

Track

Head and Neck Cancer

Sub Track

Advanced/Metastatic Disease

Clinical Trial Registration Number

NCT02252042

Citation

J Clin Oncol 37, 2019 (suppl; abstr 6026)

DOI

10.1200/JCO.2019.37.15_suppl.6026

Abstract #

6026

Poster Bd #

15

Abstract Disclosures