Safety and Antitumor Activity of the Anti–Programmed Death-1 Antibody Pembrolizumab in Patients With Advanced Esophageal Carcinoma

dc.contributor.authorDoi, Toshihiko
dc.contributor.authorPiha-Paul, Sarina A.
dc.contributor.authorJalal, Shadia I.
dc.contributor.authorSaraf, Sanatan
dc.contributor.authorLunceford, Jared
dc.contributor.authorLunceford, Minori
dc.contributor.authorBennouna, Jaafar
dc.contributor.departmentMedicine, School of Medicineen_US
dc.date.accessioned2018-09-14T17:48:32Z
dc.date.available2018-09-14T17:48:32Z
dc.date.issued2018-01
dc.description.abstractPurpose The anti–programmed death-1 antibody pembrolizumab was evaluated in KEYNOTE-028, a multicohort, phase IB study of patients with programmed death ligand-1 (PD-L1)–positive advanced solid tumors. Results from the esophageal carcinoma cohort are reported herein. Patients and Methods Eligible patients with squamous cell carcinoma or adenocarcinoma of the esophagus or gastroesophageal junction in whom standard therapy failed and who had PD-L1–positive tumors received pembrolizumab 10 mg/kg every 2 weeks for up to 2 years or until confirmed disease progression or intolerable toxicity. Response was assessed every 8 weeks up to 6 months and every 12 weeks thereafter. Primary end points were safety and overall response rate, determined by investigator review per Response Evaluation Criteria in Solid Tumors (version 1.1). Results Among 83 patients with esophageal carcinoma and samples evaluable for PD-L1 expression, 37 (45%) had PD-L1–positive tumors, and 23 were enrolled. Median age was 65 years; 78% had squamous histology; and 87% received ≥ two prior therapies for advanced/metastatic disease. As of the data cutoff (February 20, 2017), median follow-up was 7 months (range, 1 to 33 months). Nine patients (39%) experienced treatment-related adverse events, most commonly decreased appetite, decreased lymphocyte count, generalized rash, and rash (two patients [9%] each). No grade 4 adverse events or deaths were attributed to pembrolizumab. Overall response rate was 30% (95% CI, 13% to 53%); median duration of response was 15 months (range, 6 to 26 months). A six-gene interferon-γ gene expression signature analysis suggested that delayed progression and increased response occur among pembrolizumab-treated patients with higher interferon-γ composite scores. Conclusion Pembrolizumab demonstrated manageable toxicity and durable antitumor activity in patients with heavily pretreated, PD-L1–positive advanced esophageal carcinoma.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationDoi, T., Piha-Paul, S. A., Jalal, S. I., Saraf, S., Lunceford, J., Koshiji, M., & Bennouna, J. (2017). Safety and Antitumor Activity of the Anti–Programmed Death-1 Antibody Pembrolizumab in Patients With Advanced Esophageal Carcinoma. Journal of Clinical Oncology, 36(1), 61–67. https://doi.org/10.1200/JCO.2017.74.9846en_US
dc.identifier.urihttps://hdl.handle.net/1805/17316
dc.language.isoenen_US
dc.publisherASCOen_US
dc.relation.isversionof10.1200/JCO.2017.74.9846en_US
dc.relation.journalJournal of Clinical Oncologyen_US
dc.rightsPublisher Policyen_US
dc.sourcePublisheren_US
dc.subjectanti–programmed death-1 antibodyen_US
dc.subjectpembrolizumaben_US
dc.subjectesophageal carcinomaen_US
dc.titleSafety and Antitumor Activity of the Anti–Programmed Death-1 Antibody Pembrolizumab in Patients With Advanced Esophageal Carcinomaen_US
dc.typeArticleen_US
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