Chimeric Antigen Receptor T Cells Targeting CD19 and GCC in Metastatic Colorectal Cancer

IF 22.5 1区 医学 Q1 ONCOLOGY
Naifei Chen, Chengfei Pu, Lingling Zhao, Wei Li, Chang Wang, Ruihong Zhu, Tingting Liang, Chao Niu, Xi Huang, Haiyang Tang, Yizhuo Wang, Hang Yang, Beibei Jia, Xianyang Jiang, Guiting Han, Wensheng Wang, Dongqi Chen, Yiming Wang, Eric K. Rowinsky, Eugene Kennedy, Victor X. Lu, Guozhen Cui, Zhao Wu, Lei Xiao, Jiuwei Cui
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引用次数: 0

Abstract

ImportanceChimeric antigen receptor (CAR) T-cell therapy (CART) has transformed the treatment landscape of hematologic cancer, but has negligible effects for adult solid cancers. In this trial, an autologous CAR T-cell product demonstrated antitumor activity in heavily pretreated patients with metastatic colorectal cancer (mCRC).ObjectiveTo evaluate the safety and efficacy of guanylate cyclase-C (GCC19) CART in participants with metastatic colorectal cancer (mCRC).Design, Setting, and ParticipantsThis single-arm, nonrandomized, phase 1 trial was conducted at the First Hospital of Jilin University from December 3, 2020, to April 13, 2022. Data analysis was conducted from May 2022 to April 2024. Adults with relapsed and refractory mCRC expressing GCC were treated with GCC19CART, a mixture of autologous CAR T cells transduced with lentiviral vectors expressing genes that encode either CD-19 CAR or GCC CAR.Main Outcomes and MeasuresSafety and tolerability of CAR T-cell therapy targeting GCC in patients with mCRC without therapeutic options is capable of conferring a reasonable likeliness of clinical benefit. Other outcomes included objective response rate, progression-free survival, overall survival, and immune activation.ResultsOf 15 patients 9 (60%) were women, and the median (range) age was 44 (33-61) years. Treatment with GCC19CART was associated with the development of cytokine release syndrome and diarrhea in most patients, all of which were self-limited and manageable. The objective response rate was 40%, with a partial response in 2 of 8 and 4 of 7 patients treated with either 1 × 106 cells/kg or 2 × 106 cells/kg. Median overall survival was 22.8 months (95% CI, 13.4-26.1) at data cutoff; the median progress-free survival was 6.0 months in the high dose level group (95% CI, 3.0 to not available).Conclusions and RelevanceThe results of this nonrandomized clinical trial suggest that GCC19CART was safe and tolerable in heavily pretreated patients with mCRC and is the first CAR T-cell therapy known to produce objective clinical activity in refractory cancer. Given the paucity of effective therapeutics developed for colorectal cancer in recent decades, the observation that CD-19 CART target engagement can robustly induce GCC19CART target engagement sufficient to produce objective activity may serve as a foundation to develop effective cellular therapy in mCRC and other solid cancers.Trial RegistrationChinese Clinical Trial Registry: ChiCTR2000040645
靶向 CD19 和 GCC 的嵌合抗原受体 T 细胞治疗转移性结直肠癌
重要性嵌合抗原受体(CAR)T 细胞疗法(CART)改变了血液肿瘤的治疗格局,但对成人实体瘤的疗效却微乎其微。在这项试验中,一种自体CAR T细胞产品在重度预处理的转移性结直肠癌(mCRC)患者中显示出抗肿瘤活性。目的评估鸟苷酸环化酶-C(GCC19)CART在转移性结直肠癌(mCRC)患者中的安全性和有效性。数据分析于 2022 年 5 月至 2024 年 4 月进行。表达GCC的复发性和难治性mCRC成人患者接受了GCC19CART治疗,这是一种用表达编码CD-19 CAR或GCC CAR基因的慢病毒载体转导的自体CAR T细胞混合物。主要结果和测量指标在没有治疗选择的mCRC患者中,靶向GCC的CAR T细胞疗法的安全性和耐受性能够带来合理的临床获益可能性。其他结果包括客观反应率、无进展生存期、总生存期和免疫激活。结果15名患者中有9名(60%)为女性,年龄中位数(范围)为44(33-61)岁。大多数患者在接受 GCC19CART 治疗后会出现细胞因子释放综合征和腹泻,但这些症状都是自限性的,可以控制。客观反应率为40%,在接受1×106细胞/千克或2×106细胞/千克治疗的8名患者中,有2人出现部分反应,7名患者中有4人出现部分反应。数据截止时,中位总生存期为22.8个月(95% CI,13.4-26.1个月);高剂量组的中位无进展生存期为6.0个月(95% CI,3.0-不可用)。结论与意义这项非随机临床试验的结果表明,GCC19CART在重度预处理的mCRC患者中是安全和可耐受的,是已知的首个能在难治性癌症中产生客观临床活性的CAR T细胞疗法。鉴于近几十年来针对结直肠癌开发的有效疗法很少,CD-19 CART靶点参与能强有力地诱导GCC19CART靶点参与,从而产生足够的客观活性,这一观察结果可能为开发针对mCRC和其他实体癌的有效细胞疗法奠定基础:中国临床试验注册中心
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来源期刊
JAMA Oncology
JAMA Oncology Medicine-Oncology
自引率
1.80%
发文量
423
期刊介绍: JAMA Oncology is an international peer-reviewed journal that serves as the leading publication for scientists, clinicians, and trainees working in the field of oncology. It is part of the JAMA Network, a collection of peer-reviewed medical and specialty publications.
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