Novel systemic therapy against malignant pleural mesothelioma

被引:20
|
作者
Mancuso, Michael R. [1 ]
Neal, Joel W. [1 ]
机构
[1] Stanford Univ, Dept Med, Sch Med, Div Oncol, Stanford, CA 94305 USA
关键词
Mesothelioma; chemotherapy; mesothelin; immunotherapy; clinical trials; PEGYLATED ARGININE DEIMINASE; PHASE-II TRIAL; PEMETREXED PLUS CISPLATIN; HISTONE DEACETYLASE INHIBITOR; TYROSINE KINASE INHIBITOR; CUTTING-NEEDLE-BIOPSY; IMATINIB MESYLATE; ANTITUMOR-ACTIVITY; DOUBLE-BLIND; ARGININOSUCCINATE SYNTHETASE;
D O I
10.21037/tlcr.2017.06.01
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Malignant pleural mesothelioma is an aggressive tumor of the pleura with an overall poor prognosis. Even with surgical resection, for which only a subset of patients are eligible, long term disease free survival is rare. Standard first-line systemic treatment consists of a platinum analog, an anti-metabolite, and sometimes anti-angiogenic therapy, but there is currently no well-established standard therapy for refractory or relapsed disease. This review focuses on efforts to develop improved systemic therapy for the treatment of malignant pleural mesothelioma (MPM) including cytotoxic systemic therapy, a variety of tyrosine kinase inhibitors and their downstream effector pathways, pharmacologic targeting of the epigenome, novel approaches to target proteins expressed on mesothelioma cells (such as mesothelin), arginine depletion therapy, and the emerging role of immunotherapy. Overall, these studies demonstrate the challenges of improving systemic therapy for MPM and highlight the need to develop therapeutic strategies to control this disease.
引用
收藏
页码:295 / 314
页数:20
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