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Predictive role of ctDNA in esophageal squamous cell carcinoma receiving definitive chemoradiotherapy combined with toripalimab

食管鳞状细胞癌 放化疗 临床终点 肿瘤科 循环肿瘤DNA 医学 食管癌 内科学 代理终结点 临床试验 胃肠病学 癌症
作者
Baoqing Chen,Shiliang Liu,Yujia Zhu,Ruixi Wang,Xingyuan Cheng,Biqi Chen,Mihnea P. Dragomir,Yaru Zhang,Yonghong Hu,Mengzhong Liu,Qiaoqiao Li,Hong Yang,Mian Xi
出处
期刊:Nature Communications [Springer Nature]
卷期号:15 (1) 被引量:3
标识
DOI:10.1038/s41467-024-46307-7
摘要

Abstract The combination of toripalimab (an anti-PD-1 antibody) with definitive chemoradiotherapy (CRT) demonstrated encouraging efficacy against locally advanced esophageal squamous cell carcinoma (ESCC) in the EC-CRT-001 phase II trial (NCT04005170). The primary endpoint of this trial was the clinical complete response rate (cCR), and the secondary endpoints included overall survival (OS), progression-free survival (PFS), duration of response, and quality of life. The exploratory analyses of EC-CRT-001 include exploring the role of circulating tumor DNA (ctDNA) and blood-based tumor mutational burden (bTMB) in predicting the response and survival. In total, 118 blood and 35 tissue samples from 42 enrolled patients were included in the analyses. We found that ctDNA-negative patients achieved a higher cCR compared to those with detectable ctDNA during CRT (83%, 19/23 vs. 39%, 7/18; p = 0.008) or post-CRT (78%, 21/27 vs. 30%, 3/10; p = 0.017). Patients with detectable ctDNA during CRT had shorter PFS ( p = 0.014). Similarly, patients with post-CRT detectable ctDNA had a significantly shorter PFS ( p = 0.012) and worse OS ( p = 0.004). Moreover, patients with high bTMB levels during CRT had prolonged OS ( p = 0.027). In conclusion, ctDNA and bTMB have the potential to predict treatment efficacy and survival in ESCC treated with CRT and immunotherapy.
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