Ciardiello Fortunato, De Vita Ferdinando, Orditura Michele, Tortora Giampaolo
Cattedra di Oncologia Medica, Dipartimento Medico-Chirurgico di Internistica Clinica e Sperimentale F Magrassi e A Lanzara, Seconda Università degli Studi di Napoli, Naples, Italy.
Curr Opin Oncol. 2004 Mar;16(2):130-5. doi: 10.1097/00001622-200403000-00008.
The epidermal growth factor receptor is a cell membrane receptor that plays a key role in cancer development and progression. Ligand-activated epidermal growth factor receptor-dependent signaling is involved in cell proliferation, apoptosis, angiogenesis, invasion, and metastasis. Targeting the epidermal growth factor receptor represents a promising molecular approach in cancer treatment. Several antiepidermal growth factor receptor agents are in clinical development. This review focuses on the available clinical data on epidermal growth factor receptor-targeting drugs in the treatment of nonsmall cell lung cancer.
Three drugs are currently in phase 2 and phase 3 development as single agents or in combination with other anticancer therapies in nonsmall cell lung cancer patients: cetuximab (Erbitux), a chimeric human-mouse monoclonal IgG1 antibody that blocks ligand binding and functional epidermal growth factor receptor activation; and erlotinib (Tarceva) and gefitinib (Iressa), two orally bioavailable, small-molecule epidermal growth factor receptor inhibitors of tyrosine kinase enzymatic activity that prevent epidermal growth factor receptor autophosphorylation and activation. Single-agent gefitinib treatment has determined a 10 to 20% response rate and a 30 to 50% symptom improvement in previously treated, chemotherapy-refractory advanced nonsmall cell lung cancer patients. Gefitinib has been the first epidermal growth factor receptor-targeting agent to be registered as an anticancer drug in several countries, including Japan, Australia, and the United States, for the third-line treatment of chemoresistant nonsmall cell lung cancer patients.
Antiepidermal growth factor receptor has shown promising antitumor activity in nonsmall cell lung cancer patients with a mild toxicity profile. However, a series of important clinical issues such as selection of potentially responsive patients and optimal combination with conventional anticancer treatments needs to be addressed to use these drugs better in lung cancer.
表皮生长因子受体是一种细胞膜受体,在癌症发生和发展过程中起关键作用。配体激活的表皮生长因子受体依赖性信号传导参与细胞增殖、凋亡、血管生成、侵袭和转移。靶向表皮生长因子受体是癌症治疗中一种有前景的分子方法。几种抗表皮生长因子受体药物正处于临床开发阶段。本综述重点关注表皮生长因子受体靶向药物治疗非小细胞肺癌的现有临床数据。
目前有三种药物正处于2期和3期开发阶段,作为单药或与其他抗癌疗法联合用于非小细胞肺癌患者:西妥昔单抗(爱必妥),一种嵌合型人鼠单克隆IgG1抗体,可阻断配体结合和功能性表皮生长因子受体激活;厄洛替尼(特罗凯)和吉非替尼(易瑞沙),两种口服生物利用度高的小分子表皮生长因子受体酪氨酸激酶活性抑制剂,可防止表皮生长因子受体自身磷酸化和激活。单药吉非替尼治疗已确定在先前接受过治疗、对化疗耐药的晚期非小细胞肺癌患者中有效率为10%至20%,症状改善率为30%至50%。吉非替尼已成为首个在包括日本、澳大利亚和美国在内的多个国家注册为抗癌药物的表皮生长因子受体靶向药物,用于化疗耐药非小细胞肺癌患者的三线治疗。
抗表皮生长因子受体在非小细胞肺癌患者中显示出有前景的抗肿瘤活性,且毒性较轻。然而,为了在肺癌中更好地使用这些药物,需要解决一系列重要的临床问题,如选择潜在反应性患者以及与传统抗癌治疗的最佳联合。