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首页> 外文期刊>American Journal of Cancer Research >Combinational therapy of crizotinib and afatinib for malignant pleural mesothelioma
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Combinational therapy of crizotinib and afatinib for malignant pleural mesothelioma

机译:克唑替尼和阿法替尼联合治疗恶性胸膜间皮瘤

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摘要

Malignant pleural mesothelioma (MPM) is a relative rare but highly aggressive neoplasm which is associated with asbestos exposure in most patients. The majority of patients are diagnosed in advanced stages so patients neither benefit from chemotherapy (e.g. pemetrexed-platinum combination) nor from surgery. It has been reported that cellular-mesenchymal to epithelial transition factor (MET) and epidermal growth factor receptor (EGFR) were critical for MPM cell proliferation. Moreover, targeting MET and EGFR drugs have gained promising results on anti-tumor therapy. Here, a striking difference in overall survival was observed between the MET and EGFR co-expression group (median survival time = 13.5 months) and non-co-expression group (median survival time = 20.5 months). In addition, treatment with combination of crizotinib and afatinib showed stronger inhibition on cell proliferation of MPM than the treatment by either one in vitro and in vivo. In conclusion, our data illustrated that crizotinib combined with afatinib may be a potentially effective strategy for treating MPM patients with over-expression of MET and EGFR.
机译:恶性胸膜间皮瘤(MPM)是一种相对罕见但高度侵袭性的肿瘤,在大多数患者中与石棉接触有关。大多数患者被诊断为晚期,因此患者既不会从化疗(例如培美曲塞-铂联合用药)中受益,也不会从手术中受益。据报道,细胞间质至上皮转换因子(MET)和表皮生长因子受体(EGFR)对于MPM细胞增殖至关重要。此外,靶向MET和EGFR药物在抗肿瘤治疗方面取得了可喜的成果。在此,在MET和EGFR共表达组(中位生存时间= 13.5个月)和非共表达组(中位生存时间= 20.5个月)之间,观察到总体生存率存在显着差异。另外,与在体外和体内进行的治疗相比,用克唑替尼和阿法替尼的组合治疗对MPM的细胞增殖具有更强的抑制作用。总之,我们的数据表明,克唑替尼联合阿法替尼可能是治疗MET和EGFR过表达的MPM患者的潜在有效策略。

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