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恶性胸膜间皮瘤的当前化疗策略

Current chemotherapy strategies in malignant pleural mesothelioma.

作者信息

de Gooijer Cornedine Jannette, Baas Paul, Burgers Jacobus Adrianus

机构信息

Department of Thorax Oncology, Netherland Cancer Institute, Amsterdam, The Netherlands.

出版信息

Transl Lung Cancer Res. 2018 Oct;7(5):574-583. doi: 10.21037/tlcr.2018.04.10.

Abstract

Malignant pleural mesothelioma (MPM) is an aggressive malignancy with a 5-year survival rate of ~10%. Since most patients present with irresectable disease, the vast majority is treated with chemotherapy. The only registered therapy for MPM is platinum-pemetrexed doublet therapy, although only up to half of patients have clinical benefit from this palliative treatment. Of the anti-angiogenesis agents, only bevacizumab and nintedanib have shown activity with platinum-pemetrexed doublet therapy. Other anti-angiogenesis agents like thalidomide did not prolong (progression free) survival or response rate. Eventually, all patients will get a recurrence and no active second line therapy has been identified to date. The clinical benefit of (switch) maintenance therapy after first line treatment and combination strategies of different chemotherapies with angiogenesis inhibitors are currently under investigation. The major challenges are finding optimal treatment combinations and to select the adequate treatment for an individual patient. This review focusses on the current standard of chemotherapy and new systemic therapy strategies under investigation.

摘要

恶性胸膜间皮瘤(MPM)是一种侵袭性恶性肿瘤,5年生存率约为10%。由于大多数患者就诊时已无法手术切除,绝大多数患者接受化疗。MPM唯一注册的治疗方法是铂类培美曲塞双联疗法,尽管只有不到一半的患者从这种姑息治疗中获得临床益处。在抗血管生成药物中,只有贝伐单抗和尼达尼布在铂类培美曲塞双联疗法中显示出活性。其他抗血管生成药物如沙利度胺并未延长(无进展)生存期或提高缓解率。最终,所有患者都会复发,迄今为止尚未确定有效的二线治疗方法。一线治疗后(转换)维持治疗的临床益处以及不同化疗与血管生成抑制剂的联合策略目前正在研究中。主要挑战在于找到最佳治疗组合并为个体患者选择合适的治疗方法。本综述重点关注当前的化疗标准以及正在研究的新的全身治疗策略。

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