Levin Pavel A, Dowell Jonathan E
Division of Hematology/Oncology, University of Texas Southwestern Medical Center.
Section of Hematology/Oncology, Veteran Affairs North Texas Health Care System, Dallas, TX, USA.
Onco Targets Ther. 2017 Apr 7;10:2057-2066. doi: 10.2147/OTT.S113598. eCollection 2017.
Malignant pleural mesothelioma (MPM) is a rare, but aggressive cancer. Surgery and radiation offer limited benefit, and systemic chemotherapy remains the primary treatment modality for the majority of patients. Vascular endothelial growth factor (VEGF) and its receptor have been recognized as important players in the biology of this disease. Bevacizumab is a monoclonal antibody that binds VEGF and blocks its interaction with the VEGF receptor. Recent studies have shown benefit with the addition of bevacizumab to the combination of cisplatin and pemetrexed in MPM. This combination is now included in the National Comprehensive Cancer Network guidelines (with a category 2A recommendation) as a possible first-line treatment for unresectable MPM in appropriately selected patients. This review discusses the rationale behind the use of bevacizumab in MPM, as well as summarizes the pharmacology, efficacy, safety, and toxicity of bevacizumab across multiple trials. The use of small-molecule inhibitors of angiogenesis in the treatment of MPM is also discussed.
恶性胸膜间皮瘤(MPM)是一种罕见但侵袭性强的癌症。手术和放疗的益处有限,全身化疗仍然是大多数患者的主要治疗方式。血管内皮生长因子(VEGF)及其受体已被认为是该疾病生物学过程中的重要因素。贝伐单抗是一种结合VEGF并阻断其与VEGF受体相互作用的单克隆抗体。最近的研究表明,在MPM中,将贝伐单抗添加到顺铂和培美曲塞的联合方案中具有益处。这种联合方案现在已被纳入美国国立综合癌症网络指南(2A类推荐),作为适当选择的不可切除MPM患者的一种可能的一线治疗方案。本综述讨论了在MPM中使用贝伐单抗的理论依据,并总结了多项试验中贝伐单抗的药理学、疗效、安全性和毒性。还讨论了使用小分子血管生成抑制剂治疗MPM的情况。