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Erlotinib: small-molecule targeted therapy in the treatment of non-small-cell lung cancer.

机译:厄洛替尼:小分子靶向治疗非小细胞肺癌。

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BACKGROUND: Erlotinib is an oral tyrosine kinase inhibitor, targeting the human epidermal receptor type 1/ epidermal growth factor receptor, recently approved by the US Food and Drug Administration (FDA) for the treatment of patients with locally advanced or metastatic non-small-cell lung cancer (NSCLC) after the failure of more than 1 or 2 previous chemotherapeutic regimens. OBJECTIVE: The purpose of this article is to summarize the development, pharmacology, pharmacokinetics, efficacy, and adverse effects of erlotinib. METHODS: A literature search was conducted with the MEDLINE and EMBASE (1999-2005) databases using the search terms non-small-cell lung cancer, erlotinib, and epidermal growth factor receptor inhibitor. Abstracts from the American Society of Clinical Oncology and documents submitted to the FDA also were reviewed. RESULTS: BR.21, a randomized, placebo-controlled, multinational Phase III trial demonstrated clinically and statistically improved overall survival in patients with advanced or metastatic NSCLC treated with erlotinib versus placebo as second-line therapy. The erlotinib group had a median survival of 6.7 months versus a median survival of 4.7 months in the placebo group (P < 0.001). The toxicity profile of erlotinib was moderately benign, with the most commonly documented adverse events requiring dose reductions including skin rash (12%) and diarrhea (5%). Interstitial lung disease and relative fatalities were reported infrequently (0.8%) in patients receiving erlotinib. Two randomized, placebo-controlled, multicenter Phase III trials conducted in patients with locally advanced and metastatic NSCLC showed no clinical benefit with first-line administration of erlotinib plus concurrent platinum-based chemotherapy. CONCLUSIONS: For patients with NSCLC in whom more than 1 or 2 previous chemotherapeutic regimens have failed, erlotinib is an effective therapy with significant overall survival benefits. The use of erlotinib as first-line therapy in combination with platinum-based chemotherapeutic regimens, however, has failed to demonstrate efficacy in the treatment of NSCLC.
机译:背景:厄洛替尼是一种口服酪氨酸激酶抑制剂,靶向人表皮受体1型/表皮生长因子受体,最近获得美国食品和药物管理局(FDA)的批准,可用于治疗局部晚期或转移性非小细胞患者超过1或2种先前的化疗方案失败后的肺癌(NSCLC)。目的:本文的目的是概述厄洛替尼的发展,药理学,药代动力学,疗效和不良反应。方法:使用检索词非小细胞肺癌,厄洛替尼和表皮生长因子受体抑制剂,在MEDLINE和EMBASE(1999-2005)数据库中进行文献检索。还审查了美国临床肿瘤学会的摘要和提交给FDA的文件。结果:BR.21是一项随机,安慰剂对照的跨国公司III期临床试验,证明在临床或统计学上,厄洛替尼与安慰剂作为二线治疗药物治疗的晚期或转移性NSCLC患者的总生存期有所提高。厄洛替尼组的中位生存期为6.7个月,而安慰剂组的中位生存期为4.7个月(P <0.001)。厄洛替尼的毒性特征为中度良性,最常见的不良事件需要减少剂量,包括皮疹(12%)和腹泻(5%)。厄洛替尼组患者间质性肺疾病和相对死亡的报道很少(0.8%)。在患有局部晚期和转移性NSCLC的患者中进行的两项随机,安慰剂对照,多中心III期试验显示,一线给药厄洛替尼加同时进行的铂类化疗无临床益处。结论:对于先前有1或2种以上化疗方案失败的NSCLC患者,厄洛替尼是一种有效的治疗方法,具有明显的整体生存获益。然而,厄洛替尼与铂类化疗方案联合作为一线治疗的使用未能证明其在治疗NSCLC中的功效。

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