医学
内科学
肿瘤科
临床终点
毒性
结直肠癌
临床试验
免疫系统
临床研究阶段
胃肠病学
进行性疾病
细胞因子
疾病
癌症
免疫疗法
外科
生物反应调节剂
细胞因子释放综合征
存活率
体内
化疗
放射治疗
挽救疗法
原发性肿瘤
性能状态
离体
总体生存率
作者
Qianyu Zhang,Lin Lin,Wei Wang,Ling He,Lin Wang,Wenjuan Li,Qiujun Zhang,Dandan Hu,S S Wu,Wenyu Li,Shoubing Zhou,Wei J,JIng Pan,Yabei Liu,Yueyin Pan,Xiaohu Fan,Hu Liu
标识
DOI:10.1158/1078-0432.ccr-26-0854
摘要
PURPOSE: This phase 1 clinical trial aims to evaluate the safety, expansion kinetics, and preliminary efficacy of non-armored, nanobody-derived GCC-targeted CAR-T cells in patients with heavily pretreated, metastatic colorectal cancer. PATIENTS AND METHODS: In this single-arm, open-label, phase 1 clinical trial, twenty-four patients who received at least two prior lines of treatment received GCC-targeted CAR-T cells across four dose levels: 0.5×105, 1×106, 2×106,and 3×106 CAR-T cells/kg. The primary endpoint was safety; secondary endpoints included antitumor activity and pharmacokinetics. RESULTS: All patients experienced grade 3 or higher hematologic toxicity, and 75% developed cytokine release syndrome, both of which were generally manageable. Two treatment-related deaths occurred, one due to immune effector cell-associated hemophagocytic lymphohistiocytosis-like syndrome and one due to intestinal fistula following rapid tumor regression in a lesion adherent to the intestinal wall. The overall response rate (ORR) and disease control rate (DCR) reached 33% and 63%, respectively. Eight patients achieved a partial response (PR) as their best response, seven maintained stable disease (SD), and five had progressive disease (PD). Median progression-free survival (mPFS) was 57 days and median overall survival (mOS) was 190 days. Higher in vivo CAR-T expansion was associated with better disease control. Proof-of-concept activity was demonstrated, although response durability was limited and toxicity remains challenging. CONCLUSIONS: GCC-targeted CAR-T cells demonstrated encouraging antitumor activity in heavily pretreated CRC patients, with the initial data supporting GCC as a clinically actionable target. Further development will require dose selection, patient eligibility, and toxicity management optimization to improve the therapeutic profile.
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