Silvestri Gerard A, Rivera M Patricia
Medical University of South Carolina, Room 812 CSB, 171 Ashley Ave, Charleston, SC 29425, USA.
Chest. 2005 Dec;128(6):3975-84. doi: 10.1378/chest.128.6.3975.
Lung cancer is the most common cause of cancer death. The vast majority of patients present with non-small cell lung cancer (NSCLC) in advanced inoperable stages. The current first-line treatment for patients with advanced NSCLC includes chemotherapy and palliative radiotherapy, but most patients relapse and eventually succumb to the disease. Advances in our knowledge of cancer cell biology have led to the development of specific molecular-targeted therapeutic agents. Mutations in the epidermal growth factor receptor (EGFR) have been identified in NSCLC cells, and overexpression of the EGFR and its ligands is a common feature of many cancers; therefore, EGFR has become an attractive target for various antitumor strategies. Aberrant signaling from the EGFR is known to be important in the development and progression of NSCLC. Two oral EGFR inhibitors, gefitinib and erlotinib, are small-molecule agents that selectively inhibit the intracellular tyrosine kinase activity of the EGFR. Both have demonstrated antitumor activity in patients with advanced NSCLC who have failed all prior treatment regimens. In addition, the anti-EGFR monoclonal antibody cetuximab has shown promising activity in both first-line and second-line settings in patients with advanced NSCLC. Furthermore, patients with severe comorbidities who would not be eligible for systemic chemotherapy are candidates for these targeted therapies. Finally, these agents have also been shown to be effective for relieving symptoms, maintaining stable disease, and improving quality of life without the adverse events that may be associated with cytotoxic cancer therapies. This report will review the mechanism of action, indications, contraindications, patient selection, and efficacy and side effects of this new class of compounds. It is important for pulmonologists to be aware of this class of compounds, as they can provide benefit to patients with NSCLC who may not have been previously considered for antitumor therapy.
肺癌是癌症死亡的最常见原因。绝大多数患者就诊时已处于晚期无法手术阶段的非小细胞肺癌(NSCLC)。晚期NSCLC患者目前的一线治疗包括化疗和姑息性放疗,但大多数患者会复发并最终死于该疾病。我们对癌细胞生物学认识的进展导致了特定分子靶向治疗药物的开发。在NSCLC细胞中已发现表皮生长因子受体(EGFR)的突变,EGFR及其配体的过表达是许多癌症的共同特征;因此,EGFR已成为各种抗肿瘤策略的一个有吸引力的靶点。已知EGFR的异常信号传导在NSCLC的发生和发展中很重要。两种口服EGFR抑制剂吉非替尼和厄洛替尼是小分子药物,可选择性抑制EGFR的细胞内酪氨酸激酶活性。两者在所有先前治疗方案均失败的晚期NSCLC患者中均已显示出抗肿瘤活性。此外,抗EGFR单克隆抗体西妥昔单抗在晚期NSCLC患者的一线和二线治疗中均显示出有前景的活性。此外,不符合全身化疗条件的严重合并症患者是这些靶向治疗的候选者。最后,这些药物也已显示出可有效缓解症状、维持疾病稳定并改善生活质量,而不会出现可能与细胞毒性癌症治疗相关的不良事件。本报告将综述这类新化合物的作用机制、适应证、禁忌证、患者选择以及疗效和副作用。肺科医生了解这类化合物很重要,因为它们可为以前可能未被考虑进行抗肿瘤治疗的NSCLC患者带来益处。