阿替唑单抗
医学
肿瘤科
内科学
临床终点
食管癌
养生
免疫疗法
队列
放化疗
腺癌
癌症
外科
临床试验
彭布罗利珠单抗
作者
Tom van den Ende,Nicolien C. de Clercq,Mark I. van Berge Henegouwen,Suzanne S. Gisbertz,Elisabeth D. Geijsen,Rob H.A. Verhoeven,Sybren L. Meijer,Sandor Schokker,Mark P.G. Dings,Jacques Bergman,Nadia Haj Mohammad,Jelle P. Ruurda,Richard van Hillegersberg,Stella Mook,Max Nieuwdorp,Tanja D. de Gruijl,Tanya T.D. Soeratram,Bauke Ylstra,Nicole C.T. van Grieken,Maarten F. Bijlsma
标识
DOI:10.1158/1078-0432.ccr-20-4443
摘要
PURPOSE: The CROSS trial established neoadjuvant chemoradiotherapy (nCRT) for patients with resectable esophageal adenocarcinoma (rEAC). In the PERFECT trial, we investigated the feasibility and efficacy of nCRT combined with programmed-death ligand-1 (PD-L1) inhibition for rEAC. PATIENTS AND METHODS: Patients with rEAC received nCRT according to the CROSS regimen combined with five cycles of atezolizumab (1,200 mg). The primary endpoint was the feasibility of administering five cycles of atezolizumab in ≥75% patients. A propensity score-matched nCRT cohort was used to compare pathologic response, overall survival, and progression-free survival. Exploratory biomarker analysis was performed on repeated tumor biopsies. RESULTS: = 0.043). On-treatment nonresponders showed either a high number of cytotoxic lymphocytes (CTL) with a transcriptional signature consistent with expression of immune checkpoints, or a low number of CTLs. CONCLUSIONS: .
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