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“CAR T 细胞疗法在消化道癌症治疗中面临的障碍”。

"Hurdles race for CAR T-cell therapy in digestive tract cancer".

机构信息

Department of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Cancer Center, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Immunol Rev. 2023 Nov;320(1):100-119. doi: 10.1111/imr.13273. Epub 2023 Sep 11.

DOI:10.1111/imr.13273
PMID:37694970
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10846098/
Abstract

Digestive tract cancers (DTC) belong to the most investigated family of tumors. The incidence, prevalence, and mortality rate of DTC remain high, especially for patients with pancreatic cancer. Even though immunotherapy such as immune checkpoint inhibitors (ICI) have revolutionized the treatment of solid cancer types, ICI are still restricted to a very small group of patients and seem to be more efficacious in combination with chemotherapy. Cellular immunotherapy such as CAR T-cell therapy has entered clinical routine in hematological malignancies with outstanding results. There is growing interest on translating this kind of immunotherapy and success into patients with solid malignancies, such as DTC. This review attempts to describe the major advances in preclinical and clinical research with CAR T cells in DTC, considering the most relevant hurdles in each subtype of DTC.

摘要

消化道癌(DTC)属于最受研究关注的肿瘤家族之一。DTC 的发病率、患病率和死亡率仍然很高,尤其是胰腺癌患者。尽管免疫疗法,如免疫检查点抑制剂(ICI)已经彻底改变了实体瘤的治疗方法,但 ICI 仍然仅限于极少数患者,并且似乎与化疗联合使用更有效。CAR T 细胞疗法等细胞免疫疗法在血液恶性肿瘤的临床实践中取得了显著的成果。人们越来越关注将这种免疫疗法及其成功应用于实体恶性肿瘤,如 DTC。本综述试图描述 CAR T 细胞在 DTC 中的临床前和临床研究的主要进展,同时考虑到 DTC 各亚型中最相关的障碍。

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N Engl J Med. 2023 May 4;388(18):1657-1667. doi: 10.1056/NEJMoa2214963.
2
Zolbetuximab plus mFOLFOX6 in patients with CLDN18.2-positive, HER2-negative, untreated, locally advanced unresectable or metastatic gastric or gastro-oesophageal junction adenocarcinoma (SPOTLIGHT): a multicentre, randomised, double-blind, phase 3 trial.zolbetuximab 联合 mFOLFOX6 治疗 Claudin18.2 阳性、HER2 阴性、未经治疗的局部晚期不可切除或转移性胃或胃食管结合部腺癌患者(SPOTLIGHT):一项多中心、随机、双盲、III 期临床试验。
Lancet. 2023 May 20;401(10389):1655-1668. doi: 10.1016/S0140-6736(23)00620-7. Epub 2023 Apr 15.
3
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4
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5
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Sotigalimab and/or nivolumab with chemotherapy in first-line metastatic pancreatic cancer: clinical and immunologic analyses from the randomized phase 2 PRINCE trial.索托利单抗联合或不联合化疗一线治疗转移性胰腺癌:来自随机 2 期 PRINCE 试验的临床和免疫分析。
Nat Med. 2022 Jun;28(6):1167-1177. doi: 10.1038/s41591-022-01829-9. Epub 2022 Jun 3.