恶性胸膜间皮瘤的免疫检查点阻断

N. Fujimoto
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引用次数: 1

摘要

免疫调节单克隆抗体靶向免疫检查点已被证明是一种有效的抗多种癌症的策略。恶性胸膜间皮瘤(MPM)的免疫抑制肿瘤微环境提示MPM可能受益于这种免疫治疗。近年来,免疫检查点抑制剂(ICIs)在MPM患者中显示出令人鼓舞的结果。针对程序性死亡1 (PD-1)和pd -配体1 (PD-L1)的抗体显示出良好的应答、无进展生存期和总生存期。其毒性与在其他恶性肿瘤(如黑色素瘤和非小细胞肺癌)中观察到的ICIs相似,并且它们似乎是可控的。Nivolumab是一种抗pd -1抗体,在日本被批准用于对其他化疗耐药或不耐受的晚期或转移性MPM患者。未来的重要问题包括开发一种联合疗法,其中ICIs与其他药物(包括其他ICIs)联合使用,以及开发生物标志物来确定哪些患者可能反应良好,哪些患者可能会出现不可接受的毒性。不可切除的MPM的一线治疗。该研究的主要终点OS将在不久的将来报告。
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Immunocheckpoint Blockade in Malignant Pleural Mesothelioma
Targeting immunocheckpoint with immunomodulatory monoclonal antibodies has proven to be an effective antitumor strategy across a variety of cancers. The immunosuppressive tumor microenvironment in malignant pleural mesothelioma (MPM) has suggested that MPM might benefit from this kind of immunotherapy. In recent years, immunocheckpoint inhibitors (ICIs) have shown encouraging results for patients with MPM. Antibodies against programmed death 1 (PD-1) and PD-ligand 1 (PD-L1) have demonstrated favorable response, progression-free survival, and overall survival. The toxicity profiles were similar to those observed with ICIs in other malignancies, like melanoma and non-small cell lung cancer, and they appeared to be manageable. Nivolumab, an anti-PD-1 antibody, was approved in Japan for advanced or metastatic MPM patients resistant or intolerant to other chemotherapies. Important future issues include developing a combination therapy, where ICIs are combined with other agents (including other ICIs), and developing biomarkers for determining which patients might respond well and which might experience unacceptable toxicities. first-line therapy in unresectable MPM. The primary endpoint of the study, OS, will be reported in the near future.
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Suppressed Immune System Caused by Exposure to Asbestos and Malignant Mesothelioma Asbestos-Related Diseases and Blood Biomarkers Asbestos Exposure Results in Asbestosis and Usual Interstitial Pneumonia Similar to Other Causes of Pneumoconiosis Immunocheckpoint Blockade in Malignant Pleural Mesothelioma Potential Roles of Matrix Metalloproteinases in Malignant Mesothelioma
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