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靶向 CD19 和 GCC 的 CAR-T 细胞治疗转移性结直肠癌:一项非随机临床试验

英文原题:Chimeric Antigen Receptor T Cells Targeting CD19 and GCC in Metastatic Colorectal Cancer: A Nonrandomized Clinical Trial.

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Chimeric Antigen Receptor T Cells Targeting CD19 and GCC in Metastatic Colorectal Cancer: A Nonrandomized Clinical Trial.

PubMed 2024/11/01(内容时间) JAMA Oncol Q1 · IF 23.9(JCR 2025)

研究概要

这项非随机临床试验的结果提示,GCC19CART 在经重度治疗的 mCRC 患者中安全且可耐受,是已知首个在难治性癌症中产生客观临床活性的 CAR-T 细胞疗法。

中文摘要

重要性:嵌合抗原受体(CAR)T细胞疗法改变了血液系统恶性肿瘤的治疗格局,但对成人实体瘤几乎无效。本试验中,一种自体CAR-T产品在接受多线治疗的转移性结直肠癌(mCRC)患者中显示出抗肿瘤活性。目的:评估鸟苷酸环化酶C(GCC19)CAR-T在mCRC参与者中的安全性和疗效。设计、地点与参与者:该单臂、非随机I期试验于2020年12月3日至2022年4月13日在吉林大学第一医院开展。数据分析时间为2022年5月至2024年4月。纳入表达GCC的复发或难治性mCRC成人患者,给予GCC19CART;该制剂由自体CAR-T细胞混合而成,细胞经慢病毒转导后表达编码CD19 CAR或GCC CAR的基因。主要结局与指标:评估无其他治疗选择的mCRC患者接受GCC靶向CAR-T后的安全性和耐受性,以及其获得临床获益的可能性;其他结局包括客观缓解率、无进展生存期、总生存期及免疫激活。结果:15例患者中9例(60%)为女性,年龄中位数为44岁(范围33至61岁)。多数患者接受GCC19CART后发生细胞因子释放综合征及腹泻,均为自限性且可控。客观缓解率为40%;接受每千克1×10⁶或2×10⁶个细胞剂量的患者中,分别有8例中的2例和7例中的4例达到部分缓解。数据截止时总生存期中位数为22.8个月(95%置信区间13.4–26.1);高剂量组无进展生存期中位数为6.0个月(95%置信区间3.0个月至不可获得)。结论与意义:本非随机临床试验结果提示,GCC19CART在接受多线治疗的mCRC患者中安全且耐受性良好,并且据已知报道是首个在难治性癌症中产生客观临床活性的CAR-T疗法。鉴于近几十年结直肠癌有效治疗开发有限,CD19 CAR-T靶向可强有力诱导GCC19CART靶向结合并产生客观疗效的观察结果,可能为开发mCRC及其他实体瘤有效细胞疗法奠定基础。试验注册:中国临床试验注册中心ChiCTR2000040645。

展开英文摘要原文

IMPORTANCE: Chimeric 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). OBJECTIVE: To evaluate the safety and efficacy of guanylate cyclase-C (GCC19) CART in participants with metastatic colorectal cancer (mCRC). DESIGN, SETTING, AND PARTICIPANTS: This 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 MEASURES: Safety 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. RESULTS: Of 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 RELEVANCE: The 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 REGISTRATION: Chinese Clinical Trial Registry: ChiCTR2000040645.

论文信息

作者
Chen N、Pu C、Zhao L、Li W、Wang C、Zhu R、Liang T、Niu C
单位
Cancer Center, the First Hospital of Jilin University, Changchun, China.China
文献类型
I 期临床试验 · 非美国政府资助研究
期刊
JAMA oncology2024 Nov 1
原文标识
PubMed 39298141 · DOI 10.1001/jamaoncol.2024.3891