Epidermal growth factor receptor inhibitors: a new prospective in the treatment of lung cancer.

M Tiseo, M Loprevite, A Ardizzoni
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引用次数: 65

Abstract

Lung cancer is the leading cause of death worldwide. Current treatment modalities, including chemotherapy, radiotherapy and surgery, provide only limited improvement in the natural course of this disease. Therefore, the development of new therapeutic strategies is highly awaited. This review focuses on recent achievements on a novel class of anticancer drugs targeting the EGFR (Epidermal Growth Factor Receptor). The EGFR family is a group of four structurally similar growth factor receptors with tyrosine-kinase activity (EGFR, HER2/neu, ErbB-3, ErbB-4), which dimerize upon binding with a number of ligands, including EGF (Epidermal Growth Factor) and TGF (Transforming Growth Factor), allowing downstream transduction of mitogenic signals. Overexpression of EGFR and HER2 is frequently found in non-small-cell lung cancer (NSCLC), which accounts for over 80% of all malignant lung tumors, and has been associated with a worse clinical outcome. New agents developed to inhibit EGFR function include monoclonal antibodies and small-molecule receptor tyrosine-kinase inhibitors. In this review, results of most recent clinical with EGFR inhibitors including monoclonal antibodies, such as Trastuzumab (Herceptin), IMC-C225 (Cetuximab) and others (ABX-EGF, EMD 72000), and tyrosine-kinase inhibitors, such as ZD1839 (Gefitinib, Iressa), OSI-774 (Erlotinib, Tarceva) and others (CI-1033, GW2016), are summarized. In particular, final results of phase II (IDEAL 1 and 2) and III (INTACT 1 and 2) studies of ZD1839 are reported. In IDEAL trials (ZD1839 single agent in patients pre-treated with chemotherapy) there was clear evidence of tumor regression, symptoms improvement and overall clinical benefit, whereas in the two INTACT trials (ZD1839 in combination with standard platinum-based chemotherapy in chemo-naive patients) ZD1839 did not improve either survival or other clinical endpoints. Possible explanations for these contradictory results and future perspectives are discussed.

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表皮生长因子受体抑制剂:肺癌治疗的新前景。
肺癌是世界范围内导致死亡的主要原因。目前的治疗方式,包括化疗、放疗和手术,只能有限地改善这种疾病的自然病程。因此,新的治疗策略的发展备受期待。本文综述了一类以表皮生长因子受体(EGFR)为靶点的新型抗癌药物的研究进展。EGFR家族是一组四种结构相似的具有酪氨酸激酶活性的生长因子受体(EGFR, HER2/neu, ErbB-3, ErbB-4),它们与许多配体结合后二聚体化,包括表皮生长因子(EGF)和转化生长因子(TGF),允许有丝分裂信号的下游转导。EGFR和HER2过表达常见于非小细胞肺癌(NSCLC),占所有恶性肺肿瘤的80%以上,且与较差的临床预后相关。抑制EGFR功能的新药物包括单克隆抗体和小分子酪氨酸激酶受体抑制剂。在这篇综述中,总结了最近临床使用EGFR抑制剂的结果,包括单克隆抗体,如曲妥珠单抗(赫赛汀),IMC-C225(西妥昔单抗)等(ABX-EGF, EMD 72000),酪氨酸激酶抑制剂,如ZD1839(吉非替尼,易瑞沙),osii -774(厄洛替尼,特罗凯)等(CI-1033, GW2016)。特别是,报告了ZD1839的II期(IDEAL 1和2)和III期(完好无损1和2)研究的最终结果。在IDEAL试验(ZD1839单药用于化疗前治疗的患者)中,有明确的证据表明肿瘤消退、症状改善和总体临床获益,而在两项完整试验(ZD1839联合标准铂类化疗用于化疗初治患者)中,ZD1839没有改善生存或其他临床终点。对这些矛盾结果的可能解释和未来的观点进行了讨论。
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