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细胞免疫疗法及嵌合抗原受体T细胞在恶性胸膜间皮瘤中的局部给药

Cellular Immunotherapy and Locoregional Administration of CAR T-Cells in Malignant Pleural Mesothelioma.

作者信息

Belderbos Robert A, Vroman Heleen, Aerts Joachim G J V

机构信息

Department of Pulmonary Medicine, Erasmus MC Rotterdam, Rotterdam, Netherlands.

Erasmus MC Cancer Institute, Erasmus MC Rotterdam, Rotterdam, Netherlands.

出版信息

Front Oncol. 2020 Jun 3;10:777. doi: 10.3389/fonc.2020.00777. eCollection 2020.

DOI:10.3389/fonc.2020.00777
PMID:32582537
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7283907/
Abstract

Malignant pleural mesothelioma (MPM) is a treatment recalcitrant tumor with a poor overall survival (OS). Current approved treatment consists of first line chemotherapy that only modestly increases OS, illustrating the desperate need for other treatment options in MPM. Unfortunately, clinical studies that investigate the effectivity of checkpoint inhibitor (CI) treatment failed to improve clinical outcome over current applied therapies. In general, MPM is characterized as an immunological cold tumor with low T-cell infiltration, which could explain the disappointing results of clinical trials investigating CI treatment in MPM. Currently, many other therapeutic approaches, such as cellular therapies and cancer vaccines are investigated that could induce a tumor-specific immune response and increase of the number of tumor-infiltrating lymphocytes. In this review we will discuss these novel treatment approaches for MPM.

摘要

恶性胸膜间皮瘤(MPM)是一种治疗棘手的肿瘤,总体生存率(OS)较低。目前获批的治疗方法是一线化疗,其仅适度提高了OS,这表明MPM迫切需要其他治疗选择。不幸的是,研究检查点抑制剂(CI)治疗有效性的临床研究未能比当前应用的疗法改善临床结局。一般而言,MPM的特征是T细胞浸润低的免疫冷肿瘤,这可以解释在MPM中研究CI治疗的临床试验结果令人失望的原因。目前,正在研究许多其他治疗方法,如细胞疗法和癌症疫苗,它们可以诱导肿瘤特异性免疫反应并增加肿瘤浸润淋巴细胞的数量。在本综述中,我们将讨论MPM的这些新型治疗方法。

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本文引用的文献

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A multicentre randomised phase III trial comparing pembrolizumab versus single-agent chemotherapy for advanced pre-treated malignant pleural mesothelioma: the European Thoracic Oncology Platform (ETOP 9-15) PROMISE-meso trial.一项比较派姆单抗与单药化疗治疗晚期预处理恶性胸膜间皮瘤的多中心随机 III 期试验:欧洲胸部肿瘤平台(ETOP 9-15)PROMISE-meso 试验。
Ann Oncol. 2020 Dec;31(12):1734-1745. doi: 10.1016/j.annonc.2020.09.009. Epub 2020 Sep 22.
2
Phase I Study of Lentiviral-Transduced Chimeric Antigen Receptor-Modified T Cells Recognizing Mesothelin in Advanced Solid Cancers.嵌合抗原受体修饰的慢病毒转导 T 细胞识别间皮素治疗晚期实体瘤的 I 期临床研究。
Mol Ther. 2019 Nov 6;27(11):1919-1929. doi: 10.1016/j.ymthe.2019.07.015. Epub 2019 Jul 30.
3
恶性胸膜间皮瘤的局部治疗和肿瘤周围基质的调控:一种转化方法。
Int J Mol Sci. 2021 Aug 20;22(16):9014. doi: 10.3390/ijms22169014.
A multicenter, randomized, phase II/III study of dendritic cells loaded with allogeneic tumor cell lysate (MesoPher) in subjects with mesothelioma as maintenance therapy after chemotherapy: DENdritic cell Immunotherapy for Mesothelioma (DENIM) trial.一项多中心、随机、II/III期研究,在间皮瘤患者中使用负载异体肿瘤细胞裂解物(MesoPher)的树突状细胞作为化疗后的维持治疗:间皮瘤树突状细胞免疫疗法(DENIM)试验。
Transl Lung Cancer Res. 2019 Jun;8(3):280-285. doi: 10.21037/tlcr.2019.05.05.
4
Mesothelioma: Scientific clues for prevention, diagnosis, and therapy.间皮瘤:预防、诊断和治疗的科学线索。
CA Cancer J Clin. 2019 Sep;69(5):402-429. doi: 10.3322/caac.21572. Epub 2019 Jul 8.
5
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Clin Cancer Res. 2019 Oct 1;25(19):5787-5798. doi: 10.1158/1078-0432.CCR-19-0070. Epub 2019 Jul 1.
6
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Hematol Oncol. 2019 Jun;37 Suppl 1:95-100. doi: 10.1002/hon.2591.
7
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9
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10
The clinical application of cancer immunotherapy based on naturally circulating dendritic cells.基于自然循环树突状细胞的癌症免疫疗法的临床应用。
J Immunother Cancer. 2019 Apr 18;7(1):109. doi: 10.1186/s40425-019-0580-6.