Preliminary results of benmelstobart (BEN) combined with concurrent chemoradiotherapy (cCRT) versus cCRT alone as neoadjuvant therapy for esophageal squamous cell carcinoma (ESCC): A multicentre, randomised study.
Abstract
376 Background: While concurrent chemoradiotherapy (cCRT) remains the standard neoadjuvant therapy for resectable esophageal squamous cell carcinoma (ESCC), pathological complete response (pCR) rates remain suboptimal (20–30%). Immunotherapy has demonstrated efficacy in advanced ESCC, its potential synergy with cCRT in the neoadjuvant setting warrants investigation. Methods: In this multicenter, randomised, phase II trial, we planned to enroll 100 patients with resectable ESCC (T1-3N+M0/T3NanyM0). Participants were randomized 1:1 to receive either anti-PD-L1 antibody benmelstobart (1200mg, D1 and 22) + cCRT (paclitaxel 50 mg/m² + carboplatin AUC2, weekly with radiotherapy 41.4 Gy/23 fractions) or cCRT alone, stratified by cT stage (T1-2 vs T3). Surgery was performed 6-8 weeks post-treatment. The primary endpoint was pCR rate. Secondary endpoints included major pathological response (MPR), objective response rate (ORR), disease control rate (DCR), R0 resection rate, 1-year disease-free survival (DFS), 1-year overall survival (OS), completion rate of neoadjuvant therapy, and safety. A radiation de-escalation (36 Gy) was preplanned if ≥18 of the first 30 patients in BEN +cCRT group achieved pCR. Results: From October 24, 2024, to August 31, 2025, 82 patients were randomly assigned to BEN + cCRT group (n=42) or cCRT group (n=40). Thirty and 36 patients completed neoadjuvant therapy, respectively, while 7 and 4 remain on treatment. Besides, 4 patients withdrew after randomization and 1 patient withdrew without completing neoadjuvant therapy in BEN + cCRT group. Eighteen patients in the BEN +cCRT group and 24 in the cCRT group had undergone esophagectomy with postoperative pathology available. Of them, R0 resection was 100% in both groups. pCR rates were 50% (9/18) versus 42% (10/24), and MPR rates were 78% (14/18) versus 63% (15/24), respectively. Grade ≥3 treatment-related adverse events (TRAEs) were observed in 40% versus 35% of patients, respectively, with hematologic toxicity being the most common. No grade ≥3 radiation esophagitis or grade 5 TEAEs were observed. Conclusions: Neoadjuvant benmelstobart combined with cCRT shows encouraging preliminary efficacy, including high pCR and MPR rates, and a manageable safety profile in resectable ESCC. Continued enrollment and follow-up will further elucidate the regimen’s clinical benefits. Clinical trial information: NCT06637163 .
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (11)
Han Tang
Shenzhen Hospital of Shanghai University of Traditional Chinese Medicine
Yang Zhang
Peng Tang
Institut für Chemie und Biochemie, Freie Universität Berlin
Yegang Ma
Shaobin Chen
Biao Li
Beijing Key Laboratory of Theory and Technology for Advanced Batteries Materials, School of Materials Science and Engineering
Youhua Jiang
Zhejiang Cancer Hospital, Hangzhou, China
Dong Jiang
Shuoyan Liu
Shisuo Du
Zhongshan Hospital, Fudan University, Shanghai, China
Lijie Tan