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表皮生长因子受体拮抗剂治疗非小细胞肺癌的临床获益生物标志物。

Biomarkers of clinical benefit for anti-epidermal growth factor receptor agents in patients with non-small-cell lung cancer.

机构信息

Department of Medical Oncology, University General Hospital of Heraklion, PO Box 1352, Heraklion 71110, Crete, Greece.

出版信息

Br J Cancer. 2011 Jun 28;105(1):1-8. doi: 10.1038/bjc.2011.207. Epub 2011 Jun 7.

Abstract

Non-small-cell lung cancer (NSCLC) remains by far the major cause of cancer-related death in the Western world in both men and women. The majority of patients will be diagnosed with metastatic disease, and chemotherapy doublets remain the cornerstone of treatment for these patients. However, chemotherapy has a minimal impact on long-term survival and prognosis remains poor for these patients. Further improvement in treatment is likely to require incorporation of novel targeted therapies. Among these agents, inhibitors of the epidermal growth factor receptor (EGFR) have demonstrated significant activity in the first-, second- or third-line treatment of NSCLC. The purpose of current paper is to present the evidence for using several proposed molecular biomarkers as a tool for selection of NSCLC patients for anti-EGFR treatment. According to current data, EGFR mutation status appears to be the strongest predictor for the selection of NSCLC patients to first-line treatment with EGFR tyrosine kinase inhibitors vs chemotherapy. Use of other biomarkers remains investigational.

摘要

非小细胞肺癌(NSCLC)仍然是目前西方男性和女性癌症相关死亡的主要原因。大多数患者将被诊断为转移性疾病,化疗双联方案仍然是这些患者治疗的基石。然而,化疗对长期生存的影响很小,这些患者的预后仍然很差。进一步改善治疗可能需要纳入新型靶向治疗。在这些药物中,表皮生长因子受体(EGFR)抑制剂在 NSCLC 的一线、二线或三线治疗中表现出显著的活性。本文的目的是介绍使用几种提出的分子生物标志物作为选择 NSCLC 患者进行抗 EGFR 治疗的工具的证据。根据目前的数据,EGFR 突变状态似乎是选择 NSCLC 患者进行一线 EGFR 酪氨酸激酶抑制剂治疗与化疗的最强预测因素。其他生物标志物的应用仍在研究中。

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