Camrelizumab combined with concurrent chemoradiotherapy for locally recurrent esophageal cancer: A single-arm, open-label study.

e16143 Background: Local recurrence is the main failure pattern after radical treatment of esophageal cancer. There is no uniform treatment specification for such patients(pts) so far. The combination of immune checkpoint inhibitors and concurrent chemoradiotherapy (CCRT) has emerged as a novel strategy to treat esophageal cancer. This research was to evaluate the efficacy and safety of camrelizumab (ICI targeting PD-1) combined with CCRT in the treatment of locally recurrent esophageal cancer. Methods: This open clinical study planned to enroll 62 pts with locally recurrent esophageal cancer following radical treatment who aged 18-75 years with ECOG performance status of 0-1. Pts received the following treatments: camrelizumab (200 mg q2w, continuous medication until disease progression, intolerable toxicity, or withdrawal); simultaneous radiotherapy (the total radiation dose was 50-50.4 Gy, which was given by 25-28 fractions, 5 fractions per week, with 1.8-2 Gy for each fraction); chemotherapy (capecitabine, 625mg/m 2 , bid, oral, d1-5, qw, total 5 weeks). The primary endpoint was progression-free survival (PFS). Secondary endpoints included overall survival (OS), objective response rate (ORR) ,disease control rate (DCR), and safety. Results: Between Feb 2022 and Jan 2025, 35 pts with a median age of 65 years old had been enrolled. Among the evaluable pts, the ORR was 58.6% (17/29), the DCR was 86.2% (25/29). With a median follow-up of 18.0 months (95% CI 6.8-29.2), the median PFS was 9.8 months (95% CI 6.8–12.8), the median OS had not yet reached in the full analysis set. The incidence of any grade adverse events(AEs) was 94.3% (33/35) and that of grade ≥3 AEs was 68.6% (24/35). The most common AEs included lymphocyte count decreased (29/35, 82.9%) and white blood cell count decreased (19/35, 54.3%). The most grade ≥3 AEs was lymphocyte count decreased (20/35, 57.1%) and white blood cell count decreased (4/35, 11.4%). Conclusions: Current results suggested the promising efficacy and acceptable safety of camrelizumab combined with CCRT in pts with locally recurrent esophageal cancer. The study enrollment is ongoing, and further survival and safety data will be reported in the future. Clinical trial information: NCT04390945 .

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Journal
Journal of Clinical Oncology
Published
2025-05-28
DOI
https://doi.org/10.1200/jco.2025.43.16_suppl.e16143
Primary Topic
Esophageal Cancer Research and Treatment
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article
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article

Camrelizumab combined with concurrent chemoradiotherapy for locally recurrent esophageal cancer: A single-arm, open-label study.

Lei Ni, Anping Zheng, Shuoguo Li, Chuntao Tian et al.
Journal of Clinical Oncology
Esophageal Cancer Research and Treatment
article

Camrelizumab combined with concurrent chemoradiotherapy for locally recurrent esophageal cancer: A single-arm, open-label study.

Lei Ni, Anping Zheng, Shuoguo Li, Chuntao Tian, Hong Ge, Kefeng Guo, Shegan Gao, Liuyan Li, Jianguang Ma, Junqian Zhang, Ruinuo Jia, Yaowen Zhang, Jingxia Li, Zhiwei Chang, Xiaohong Wang, Xiaobing Chen, Jianzheng Wang, Jun Yao, Manxi Sheng
article en

Abstract

e16143 Background: Local recurrence is the main failure pattern after radical treatment of esophageal cancer. There is no uniform treatment specification for such patients(pts) so far. The combination of immune checkpoint inhibitors and concurrent chemoradiotherapy (CCRT) has emerged as a novel strategy to treat esophageal cancer. This research was to evaluate the efficacy and safety of camrelizumab (ICI targeting PD-1) combined with CCRT in the treatment of locally recurrent esophageal cancer. Methods: This open clinical study planned to enroll 62 pts with locally recurrent esophageal cancer following radical treatment who aged 18-75 years with ECOG performance status of 0-1. Pts received the following treatments: camrelizumab (200 mg q2w, continuous medication until disease progression, intolerable toxicity, or withdrawal); simultaneous radiotherapy (the total radiation dose was 50-50.4 Gy, which was given by 25-28 fractions, 5 fractions per week, with 1.8-2 Gy for each fraction); chemotherapy (capecitabine, 625mg/m 2 , bid, oral, d1-5, qw, total 5 weeks). The primary endpoint was progression-free survival (PFS). Secondary endpoints included overall survival (OS), objective response rate (ORR) ,disease control rate (DCR), and safety. Results: Between Feb 2022 and Jan 2025, 35 pts with a median age of 65 years old had been enrolled. Among the evaluable pts, the ORR was 58.6% (17/29), the DCR was 86.2% (25/29). With a median follow-up of 18.0 months (95% CI 6.8-29.2), the median PFS was 9.8 months (95% CI 6.8–12.8), the median OS had not yet reached in the full analysis set. The incidence of any grade adverse events(AEs) was 94.3% (33/35) and that of grade ≥3 AEs was 68.6% (24/35). The most common AEs included lymphocyte count decreased (29/35, 82.9%) and white blood cell count decreased (19/35, 54.3%). The most grade ≥3 AEs was lymphocyte count decreased (20/35, 57.1%) and white blood cell count decreased (4/35, 11.4%). Conclusions: Current results suggested the promising efficacy and acceptable safety of camrelizumab combined with CCRT in pts with locally recurrent esophageal cancer. The study enrollment is ongoing, and further survival and safety data will be reported in the future. Clinical trial information: NCT04390945 .

Journal of Clinical OncologyVol. 43(16_suppl)
Henan University of Science and Technology (CN), Henan University (CN), Zhengzhou University (CN), Xian Central Hospital (CN), First Affiliated Hospital of Henan University of Science and Technology (CN), Henan Cancer Hospital (CN), First Affiliated Hospital of Zhengzhou University (CN), Anyang Tumor Hospital (CN)
Openalex Percentile: Top 79%
Esophageal Cancer Research and Treatment
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