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Population pharmacokinetics and exposure-response relationship of amatuximab, an anti-mesothelin monoclonal antibody, in patients with malignant pleural mesothelioma and its application in dose selection.抗间皮素单克隆抗体 amatuximab 在恶性胸膜间皮瘤患者中的群体药代动力学及暴露-反应关系及其在剂量选择中的应用
Cancer Chemother Pharmacol. 2016 Apr;77(4):733-43. doi: 10.1007/s00280-016-2984-z. Epub 2016 Feb 22.
2
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Lancet. 2016 Apr 2;387(10026):1405-1414. doi: 10.1016/S0140-6736(15)01238-6. Epub 2015 Dec 21.
3
Vorinostat in patients with advanced malignant pleural mesothelioma who have progressed on previous chemotherapy (VANTAGE-014): a phase 3, double-blind, randomised, placebo-controlled trial.沃利替尼治疗表皮生长因子受体突变阳性的局部晚期或转移性非小细胞肺癌患者的随机、双盲、安慰剂对照、多中心Ⅲ期临床研究
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8
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Mol Cancer Ther. 2014 Jun;13(6):1537-48. doi: 10.1158/1535-7163.MCT-13-0926. Epub 2014 Apr 8.
10
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靶向治疗:恶性胸膜间皮瘤的新药或药物新组合

Target therapy: new drugs or new combinations of drugs in malignant pleural mesothelioma.

作者信息

Zucali Paolo A

机构信息

Department of Oncology, Humanitas Clinical and Research Hospital, Rozzano, Milan, Italy.

出版信息

J Thorac Dis. 2018 Jan;10(Suppl 2):S311-S321. doi: 10.21037/jtd.2017.10.131.

DOI:10.21037/jtd.2017.10.131
PMID:29507801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5830552/
Abstract

Malignant pleural mesothelioma (MPM) is a disease with a poor prognosis due to its aggressive nature. The management of patients with MPM is controversial. Considering that the contribution of surgery and radiation therapy in the management of this disease is not yet established, systemic treatments are predominantly considered during the course of MPM. Unfortunately, the currently therapeutic armamentarium is scarce and its outcomes still appear modest. New treatment strategies are needed. In preclinical setting, cell cycle regulation, apoptosis, growth factor pathways, and angiogenesis pathways involved in the development of MPM have been identified. However, in clinical setting, several drugs targeting these pathways resulted without a significant activity. A deeper knowledge of the biology and pathogenesis of this disease is required to develop more effective tools for diagnosis, therapy and prevention. This paper reviews therapeutic advances in MPM, with a particular focus on new drugs and new association of drugs of target therapy.

摘要

恶性胸膜间皮瘤(MPM)是一种预后较差的疾病,因其具有侵袭性。MPM患者的治疗存在争议。鉴于手术和放射治疗在该疾病治疗中的作用尚未明确,在MPM病程中主要考虑采用全身治疗。不幸的是,目前的治疗手段有限,其治疗效果仍然一般。需要新的治疗策略。在临床前研究中,已经确定了参与MPM发生发展的细胞周期调控、细胞凋亡、生长因子途径和血管生成途径。然而,在临床研究中,几种针对这些途径的药物并未显示出显著活性。需要更深入了解该疾病的生物学特性和发病机制,以开发更有效的诊断、治疗和预防工具。本文综述了MPM的治疗进展,特别关注新药和靶向治疗药物的新联合应用。