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本文引用的文献

1
First-line nivolumab plus ipilimumab in unresectable malignant pleural mesothelioma (CheckMate 743): a multicentre, randomised, open-label, phase 3 trial.一线纳武利尤单抗联合伊匹单抗治疗不可切除恶性胸膜间皮瘤(CheckMate 743):一项多中心、随机、开放标签、III 期临床试验。
Lancet. 2021 Jan 30;397(10272):375-386. doi: 10.1016/S0140-6736(20)32714-8. Epub 2021 Jan 21.
2
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.
3
Association of tumour mutational burden with outcomes in patients with advanced solid tumours treated with pembrolizumab: prospective biomarker analysis of the multicohort, open-label, phase 2 KEYNOTE-158 study.帕博利珠单抗治疗的晚期实体瘤患者肿瘤突变负荷与结局的相关性:多队列、开放标签、Ⅱ期 KEYNOTE-158 研究的前瞻性生物标志物分析。
Lancet Oncol. 2020 Oct;21(10):1353-1365. doi: 10.1016/S1470-2045(20)30445-9. Epub 2020 Sep 10.
4
Durvalumab with first-line chemotherapy in previously untreated malignant pleural mesothelioma (DREAM): a multicentre, single-arm, phase 2 trial with a safety run-in.度伐利尤单抗联合一线化疗用于未经治疗的恶性胸膜间皮瘤(DREAM):一项多中心、单臂、Ⅱ期、有安全爬坡阶段的研究
Lancet Oncol. 2020 Sep;21(9):1213-1223. doi: 10.1016/S1470-2045(20)30462-9.
5
Malignant Pleural Mesothelioma: Genetic and Microenviromental Heterogeneity as an Unexpected Reading Frame and Therapeutic Challenge.恶性胸膜间皮瘤:遗传和微环境异质性作为意外的阅读框架和治疗挑战
Cancers (Basel). 2020 May 7;12(5):1186. doi: 10.3390/cancers12051186.
6
Immunotherapy for mesothelioma: a critical review of current clinical trials and future perspectives.间皮瘤的免疫疗法:对当前临床试验及未来前景的批判性综述
Transl Lung Cancer Res. 2020 Feb;9(Suppl 1):S100-S119. doi: 10.21037/tlcr.2019.11.23.
7
Application of immunohistochemistry in diagnosis and management of malignant mesothelioma.免疫组织化学在恶性间皮瘤诊断与管理中的应用。
Transl Lung Cancer Res. 2020 Feb;9(Suppl 1):S3-S27. doi: 10.21037/tlcr.2019.11.29.
8
How I treat malignant pleural mesothelioma.我如何治疗恶性胸膜间皮瘤。
ESMO Open. 2020 Mar;4(Suppl 2):e000669. doi: 10.1136/esmoopen-2019-000669.
9
Immunotherapy in Malignant Pleural Mesothelioma.恶性胸膜间皮瘤的免疫治疗
Front Oncol. 2020 Feb 21;10:187. doi: 10.3389/fonc.2020.00187. eCollection 2020.
10
Five-Year Survival with Combined Nivolumab and Ipilimumab in Advanced Melanoma.纳武利尤单抗联合伊匹木单抗治疗晚期黑色素瘤的 5 年生存数据
N Engl J Med. 2019 Oct 17;381(16):1535-1546. doi: 10.1056/NEJMoa1910836. Epub 2019 Sep 28.

免疫疗法的浪潮席卷间皮瘤。

Tsunami of immunotherapy reaches mesothelioma.

作者信息

Mielgo-Rubio Xabier, Cardeña Gutiérrez Ana, Sotelo Peña Verónica, Sánchez Becerra Maria Virginia, González López Andrea María, Rosero Adriana, Trujillo-Reyes Juan Carlos, Couñago Felipe

机构信息

Department of Medical Oncology, Hospital Universitario Fundación Alcorcón, Alcorcón 28922, Madrid, Spain.

Department of Medical Oncology, Hospital Universitario Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Canarias 38010, Spain.

出版信息

World J Clin Oncol. 2022 Apr 24;13(4):267-275. doi: 10.5306/wjco.v13.i4.267.

DOI:10.5306/wjco.v13.i4.267
PMID:35582652
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9052072/
Abstract

Malignant pleural mesothelioma (MPM) is the most common type of malignant mesothelioma. It is a rare tumor linked to asbestos exposure and is associated with a poor prognosis. Until very recently, patients with advanced or unresectable disease had limited treatment options, primarily based on doublet chemotherapy with cisplatin and pemetrexed. In 2020 and 2021, after more than a decade with no major advances or new drugs, two phase III clinical trials published results positioning immunotherapy as a promising option for the first- and second-line treatment of MPM. Immunotherapy has revolutionized the treatment of many cancers and is also showing encouraging results in malignant mesothelioma. Both immune checkpoint inhibition and dual cytotoxic T-lymphocyte-associated antigen 4 and programmed death-ligand 1 pathway blockade resulted in significantly improved overall survival in randomized phase III trials. In the CheckMate 743 trial, first-line therapy with nivolumab plus ipilimumab outperformed standard chemotherapy, while in the CONFIRM trial, nivolumab outperformed placebo in patients previously treated with chemotherapy. These two trials represent a major milestone in the treatment of MPM and are set to position immunotherapy as a viable alternative for treatment-naïve patients and patients with progressive disease after chemotherapy.

摘要

恶性胸膜间皮瘤(MPM)是最常见的恶性间皮瘤类型。它是一种与石棉暴露相关的罕见肿瘤,预后较差。直到最近,晚期或不可切除疾病的患者治疗选择有限,主要基于顺铂和培美曲塞的双联化疗。在经历了十多年没有重大进展或新药的情况后,2020年和2021年,两项III期临床试验公布了结果,将免疫疗法定位为MPM一线和二线治疗的有前景选择。免疫疗法彻底改变了许多癌症的治疗方式,在恶性间皮瘤中也显示出令人鼓舞的结果。在随机III期试验中,免疫检查点抑制以及双重细胞毒性T淋巴细胞相关抗原4和程序性死亡配体1通路阻断均导致总生存期显著改善。在CheckMate 743试验中,纳武利尤单抗加伊匹木单抗的一线治疗优于标准化疗,而在CONFIRM试验中,纳武利尤单抗在先前接受化疗的患者中优于安慰剂。这两项试验代表了MPM治疗的一个重要里程碑,并将使免疫疗法成为初治患者和化疗后疾病进展患者的可行替代治疗方法。