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Prospective study of second-line chemotherapy for non-small cell lung cancer selected according to EGFR gene status

机译:根据EGFR基因状态选择非小细胞肺癌二线化疗的前瞻性研究

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Non-small cell lung cancer (NSCLC) is the leading cause of cancer death in Japan. Current chemotherapy regimens for metastatic NSCLC are not particularly effective, and the disease cannot be cured even with the most effective platinum and new combination chemotherapies. The epidermal growth factor receptor (EGFR) superfamily has long been regarded as a potential therapeutic target in solid tumors. Several molecules that can inhibit the EGFR tyrosine kinase domain have been synthesized. These inhibitors include gefitinib (Gef) and erlotinib, both of which are orally active and can produce an objective response in previously treated or untreated advanced NSCLC(l-4). A previous randomized study demonstrated that addition of Gef to standard platinum-based chemotherapy did not improve the outcome of patients with NSCLC( 5,6). However, a randomized study demonstrated a non-inferior survival effect of Gef treatment as a second-line chemotherapy in comparison with docetaxel in NSCLC patients (7) and Gef was approved a treatment of second-line chemotherapy in Japan.
机译:非小细胞肺癌(NSCLC)是日本癌症死亡的主要原因。转移性NSCLC的当前化疗方案并不是特别有效,即使具有最有效的铂和新的组合化疗,疾病也不能治愈。表皮生长因子受体(EGFR)超家族长期以来被认为是固体瘤中的潜在治疗靶标。已经合成了可以抑制EGFR酪氨酸激酶结构域的几种分子。这些抑制剂包括吉非替尼(GEF)和Erlotinib,两者都是口服活性的,并且可以在先前治疗或未治疗的先进NSCLC(L-4)中产生客观反应。先前的随机研究表明,添加GEF到标准铂基化学疗法并未改善NSCLC患者的结果(5,6)。然而,随机研究表明,与NSCLC患者的多西紫杉醇相比,GEF治疗的非劣质生存效应是二线化疗(7),GEF批准了日本二线化疗的治疗。

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