Author
Listed:
- Peiyuan Wang
(Fujian Cancer Hospital
Fujian Key Laboratory of Translational Cancer Medicine
Fujian Provincial Key Laboratory of Tumor Biotherapy
Fujian Cancer Hospital)
- Yujie Chen
(Fujian Cancer Hospital)
- Feng Wang
(Fujian Cancer Hospital)
- Mingqiu Chen
(Fujian Cancer Hospital)
- Buhong Zheng
(Fujian Cancer Hospital)
- Derong Zhang
(Fujian Cancer Hospital)
- Qingfeng Zheng
(Fujian Cancer Hospital)
- Jiezhong Wang
(Fujian Cancer Hospital)
- Junqiang Chen
(Fujian Cancer Hospital)
- Huaxin Cai
(Nan’an Hospital)
- Junhua Liu
(The No.2 Hospital of Longhai City)
- Wenshan Zhang
(Zhangzhou Affiliated Hospital of Fujian Medical University)
- Changhong Lian
(Heping Hospital Affiliated to Changzhi Medical College)
- Juhui Chen
(Fujian Cancer Hospital)
- Yu Lin
(Fujian Cancer Hospital)
- Yuanji Xu
(Fujian Cancer Hospital)
- Rongfang Huang
(Fujian Cancer Hospital)
- Mengxia Lei
(Fujian Cancer Hospital)
- Peng Chen
(Fujian Cancer Hospital)
- Hao He
(Fujian Cancer Hospital)
- Hui Lin
(Fujian Cancer Hospital)
- Xiaofeng Chen
(Fujian Cancer Hospital)
- Hang Zhou
(Fujian Cancer Hospital)
- Weijie Chen
(Fujian Cancer Hospital)
- Wenwei Wei
(Fujian Cancer Hospital)
- Fengnian Zhuang
(Fujian Cancer Hospital)
- Junpeng Lin
(Fujian Cancer Hospital)
- Canhua Huang
(Nan’an Hospital)
- Ni Guan
(Jiangsu Hengrui Pharmaceuticals Co. Ltd)
- Jin Yan
(Jiangsu Hengrui Pharmaceuticals Co. Ltd)
- Shujun Liang
(Jiangsu Hengrui Pharmaceuticals Co. Ltd)
- Shuoyan Liu
(Fujian Cancer Hospital)
- Jiancheng Li
(Fujian Cancer Hospital)
Abstract
Several studies have evaluated PD-1 inhibitors plus chemotherapy as neoadjuvant treatment for locally advanced esophageal squamous cell carcinoma (ESCC), but comparative data with chemoradiotherapy (CRT) remain limited. This multicenter, randomized, open-label, phase 2 non-inferiority trial (REVO, NCT05007145) assessed the efficacy and safety of neoadjuvant camrelizumab plus chemotherapy (ICT) versus CRT in patients with resectable, locally advanced ESCC. A total of 104 patients were randomized to ICT (camrelizumab, nab-paclitaxel, cisplatin) or CRT (nab-paclitaxel, cisplatin, radiotherapy). The primary endpoint was pathologic complete response (pCR). ICT achieved a pCR rate of 32.7% versus 34.6% with CRT (rate ratio 0.94, 90% CI 0.6–1.49), demonstrating non-inferiority and meeting the pre-specified primary endpoint. Major pathologic response was observed in 42.3% of ICT patients and 57.7% of CRT patients, with R0 resection achieved in 100% of both groups. 1-year disease-free survival was 89.1% versus 78.2%, and 1-year overall survival was 100% versus 92.3% for ICT and CRT, respectively. Grade ≥3 treatment-related adverse events occurred in 19.2% of ICT patients and 33.3% of CRT patients, and surgical complications were reported in 31.1% and 35.9%, respectively. These findings indicate that ICT is a safe and effective neoadjuvant strategy for resectable ESCC with a more favorable safety profile.
Suggested Citation
Peiyuan Wang & Yujie Chen & Feng Wang & Mingqiu Chen & Buhong Zheng & Derong Zhang & Qingfeng Zheng & Jiezhong Wang & Junqiang Chen & Huaxin Cai & Junhua Liu & Wenshan Zhang & Changhong Lian & Juhui C, 2025.
"Camrelizumab plus chemotherapy versus chemoradiotherapy as neoadjuvant therapy for resectable esophageal squamous cell carcinoma: Phase 2 randomized trial (REVO),"
Nature Communications, Nature, vol. 16(1), pages 1-8, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-64660-z
DOI: 10.1038/s41467-025-64660-z
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