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Multicenter, single-arm, phase II trial of camrelizumab and chemotherapy as neoadjuvant treatment for locally advanced esophageal squamous cell carcinoma

BACKGROUND: Camrelizumab and chemotherapy demonstrated durable antitumor activity with a manageable safety profile as first-line treatment in patients with advanced esophageal squamous cell carcinoma (ESCC). This study aimed to evaluate the safety and efficacy of camrelizumab plus neoadjuvant chemot...

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Autores principales: Liu, Jun, Yang, Yang, Liu, Zhichao, Fu, Xiaolong, Cai, Xiaoyue, Li, Hongxuan, Zhu, Li, Shen, Yan, Zhang, Hong, Sun, Yifeng, Chen, Hezhong, Yu, Bentong, Zhang, Renquan, Shao, Jinchen, Zhang, Ming, Li, Zhigang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961177/
https://www.ncbi.nlm.nih.gov/pubmed/35338088
http://dx.doi.org/10.1136/jitc-2021-004291
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author Liu, Jun
Yang, Yang
Liu, Zhichao
Fu, Xiaolong
Cai, Xiaoyue
Li, Hongxuan
Zhu, Li
Shen, Yan
Zhang, Hong
Sun, Yifeng
Chen, Hezhong
Yu, Bentong
Zhang, Renquan
Shao, Jinchen
Zhang, Ming
Li, Zhigang
author_facet Liu, Jun
Yang, Yang
Liu, Zhichao
Fu, Xiaolong
Cai, Xiaoyue
Li, Hongxuan
Zhu, Li
Shen, Yan
Zhang, Hong
Sun, Yifeng
Chen, Hezhong
Yu, Bentong
Zhang, Renquan
Shao, Jinchen
Zhang, Ming
Li, Zhigang
author_sort Liu, Jun
collection PubMed
description BACKGROUND: Camrelizumab and chemotherapy demonstrated durable antitumor activity with a manageable safety profile as first-line treatment in patients with advanced esophageal squamous cell carcinoma (ESCC). This study aimed to evaluate the safety and efficacy of camrelizumab plus neoadjuvant chemotherapy, using pathologically complete response (pCR) as primary endpoint, in the treatment for locally advanced ESCC. METHODS: Patients with locally advanced but resectable thoracic ESCC, staged as T1b-4a, N2-3 (≥3 stations), and M0 or M1 lymph node metastasis (confined to the supraclavicular lymph nodes) were enrolled. Eligible patients received intravenous camrelizumab (200 mg, day 1) plus nab-paclitaxel (100 mg/m(2), day 1, 8, 15) and carboplatin (area under curve of 5 mg/mL/min, day 1) of each 21-days cycle, for two cycles before surgery. The primary endpoint is pCR rate in the per-protocol population. Safety was assessed in the modified intention-to-treat population that was treated with at least one dose of camrelizumab. RESULTS: From November 20, 2019 to December 22, 2020, 60 patients were enrolled. 55 (91.7%) patients completed the full two-cycle treatment successfully. 51 patients underwent surgery and R0 resection was achieved in 50 (98.0%) patients. pCR (ypT0N0) was identified in 20 (39.2%) patients and 5 (9.8%) patients had complete response of the primary tumor but residual disease in lymph nodes alone (ypT0N+). 58 patients (96.7%) had any-grade treatment-related adverse events (TRAEs), with the most common being leukocytopenia (86.7%). 34 patients (56.7%) had adverse events of grade 3 or worse, and one patient (1.7%) occurred a grade 5 adverse event. There was no in-hospital and postoperative 30-day as well as 90-day mortality. CONCLUSIONS: The robust antitumor activity of camrelizumab and chemotherapy was confirmed and demonstrated without unexpected safety signals. Our findings established camrelizumab and chemotherapy as a promising neoadjuvant treatment for locally advanced ESCC. TRIAL REGISTRATION NUMBER: ChiCTR1900026240.
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spelling pubmed-89611772022-04-11 Multicenter, single-arm, phase II trial of camrelizumab and chemotherapy as neoadjuvant treatment for locally advanced esophageal squamous cell carcinoma Liu, Jun Yang, Yang Liu, Zhichao Fu, Xiaolong Cai, Xiaoyue Li, Hongxuan Zhu, Li Shen, Yan Zhang, Hong Sun, Yifeng Chen, Hezhong Yu, Bentong Zhang, Renquan Shao, Jinchen Zhang, Ming Li, Zhigang J Immunother Cancer Clinical/Translational Cancer Immunotherapy BACKGROUND: Camrelizumab and chemotherapy demonstrated durable antitumor activity with a manageable safety profile as first-line treatment in patients with advanced esophageal squamous cell carcinoma (ESCC). This study aimed to evaluate the safety and efficacy of camrelizumab plus neoadjuvant chemotherapy, using pathologically complete response (pCR) as primary endpoint, in the treatment for locally advanced ESCC. METHODS: Patients with locally advanced but resectable thoracic ESCC, staged as T1b-4a, N2-3 (≥3 stations), and M0 or M1 lymph node metastasis (confined to the supraclavicular lymph nodes) were enrolled. Eligible patients received intravenous camrelizumab (200 mg, day 1) plus nab-paclitaxel (100 mg/m(2), day 1, 8, 15) and carboplatin (area under curve of 5 mg/mL/min, day 1) of each 21-days cycle, for two cycles before surgery. The primary endpoint is pCR rate in the per-protocol population. Safety was assessed in the modified intention-to-treat population that was treated with at least one dose of camrelizumab. RESULTS: From November 20, 2019 to December 22, 2020, 60 patients were enrolled. 55 (91.7%) patients completed the full two-cycle treatment successfully. 51 patients underwent surgery and R0 resection was achieved in 50 (98.0%) patients. pCR (ypT0N0) was identified in 20 (39.2%) patients and 5 (9.8%) patients had complete response of the primary tumor but residual disease in lymph nodes alone (ypT0N+). 58 patients (96.7%) had any-grade treatment-related adverse events (TRAEs), with the most common being leukocytopenia (86.7%). 34 patients (56.7%) had adverse events of grade 3 or worse, and one patient (1.7%) occurred a grade 5 adverse event. There was no in-hospital and postoperative 30-day as well as 90-day mortality. CONCLUSIONS: The robust antitumor activity of camrelizumab and chemotherapy was confirmed and demonstrated without unexpected safety signals. Our findings established camrelizumab and chemotherapy as a promising neoadjuvant treatment for locally advanced ESCC. TRIAL REGISTRATION NUMBER: ChiCTR1900026240. BMJ Publishing Group 2022-03-24 /pmc/articles/PMC8961177/ /pubmed/35338088 http://dx.doi.org/10.1136/jitc-2021-004291 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Clinical/Translational Cancer Immunotherapy
Liu, Jun
Yang, Yang
Liu, Zhichao
Fu, Xiaolong
Cai, Xiaoyue
Li, Hongxuan
Zhu, Li
Shen, Yan
Zhang, Hong
Sun, Yifeng
Chen, Hezhong
Yu, Bentong
Zhang, Renquan
Shao, Jinchen
Zhang, Ming
Li, Zhigang
Multicenter, single-arm, phase II trial of camrelizumab and chemotherapy as neoadjuvant treatment for locally advanced esophageal squamous cell carcinoma
title Multicenter, single-arm, phase II trial of camrelizumab and chemotherapy as neoadjuvant treatment for locally advanced esophageal squamous cell carcinoma
title_full Multicenter, single-arm, phase II trial of camrelizumab and chemotherapy as neoadjuvant treatment for locally advanced esophageal squamous cell carcinoma
title_fullStr Multicenter, single-arm, phase II trial of camrelizumab and chemotherapy as neoadjuvant treatment for locally advanced esophageal squamous cell carcinoma
title_full_unstemmed Multicenter, single-arm, phase II trial of camrelizumab and chemotherapy as neoadjuvant treatment for locally advanced esophageal squamous cell carcinoma
title_short Multicenter, single-arm, phase II trial of camrelizumab and chemotherapy as neoadjuvant treatment for locally advanced esophageal squamous cell carcinoma
title_sort multicenter, single-arm, phase ii trial of camrelizumab and chemotherapy as neoadjuvant treatment for locally advanced esophageal squamous cell carcinoma
topic Clinical/Translational Cancer Immunotherapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961177/
https://www.ncbi.nlm.nih.gov/pubmed/35338088
http://dx.doi.org/10.1136/jitc-2021-004291
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