Palayekar M J, Herzog T J
Department of Obstetrics and Gynecology, Saint Peter's University Hospital, New Brunswick, New Jersey, USA.
Int J Gynecol Cancer. 2008 Sep-Oct;18(5):879-90. doi: 10.1111/j.1525-1438.2007.01144.x. Epub 2007 Dec 5.
Epidermal growth factor receptor (EGFR) inhibitors are a new biologically targeted therapy, which may offer new hope in the treatment of patients with advanced or recurrent ovarian cancers. In this review, we summarize and discuss the results of research to date on EGFR inhibitors with particular emphasis on ovarian cancer. We reviewed data identified by searches of MEDLINE, PubMed, and abstracts from the proceedings of the American Society of Clinical Oncology meetings from 1998 to 2006, with the search terms "Ovarian Cancer,""EGFR,""gefitinib, ZD1839, Iressa,""erlotinib, OSI-774, Tarceva,""CI-1033,"" GW 572016, lapatinib,""PKI-166,""EKB 569,""anti-EGFR antibodies,""trastuzumab, Herceptin,""cetuximab, Erbitux, IMC-C225,""matuzumab, EMD 72000,""panitumamab, ABX-EGF,""pertuzumab," and "vandetanib, rINN, Zactima, ZD6474." Phase II trials of both small molecule inhibitors of EGFR- and antibody-based inhibitors are currently ongoing in ovarian cancer and emerging data suggest that their activity in unselected women with advanced or recurrent ovarian cancer is modest, when utilized as a single agent. It is possible that these agents will be highly effective in smaller subsets of patients whose tumors are dependent on EGFR signaling, perhaps through activating mutations in EGFR or its downstream pathway. Targeted therapy with EGFR inhibitors is an untapped potential resource in the treatment of advanced or recurrent ovarian cancer. Ongoing trials will elucidate the most effective strategies to use these agents individually or in combination with traditional chemotherapeutic agents.
表皮生长因子受体(EGFR)抑制剂是一种新型生物靶向治疗药物,有望为晚期或复发性卵巢癌患者的治疗带来新希望。在本综述中,我们总结并讨论了迄今为止关于EGFR抑制剂的研究结果,特别关注了卵巢癌。我们检索了MEDLINE、PubMed以及1998年至2006年美国临床肿瘤学会会议论文摘要中的数据,检索词包括“卵巢癌”“EGFR”“吉非替尼、ZD1839、易瑞沙”“厄洛替尼、OSI-774、特罗凯”“CI-1033”“GW 572016、拉帕替尼”“PKI-166”“EKB 569”“抗EGFR抗体”“曲妥珠单抗、赫赛汀”“西妥昔单抗、爱必妥、IMC-C225”“美妥珠单抗、EMD 72000”“帕尼单抗、ABX-EGF”“帕妥珠单抗”以及“凡德他尼、rINN、Zactima、ZD6474”。目前,EGFR小分子抑制剂和基于抗体的抑制剂在卵巢癌中的II期试验正在进行,新出现的数据表明,作为单一药物使用时,它们在未经过选择的晚期或复发性卵巢癌女性患者中的活性一般。这些药物可能在肿瘤依赖EGFR信号传导的较小患者亚组中非常有效,也许是通过EGFR或其下游途径的激活突变。EGFR抑制剂的靶向治疗是晚期或复发性卵巢癌治疗中尚未开发的潜在资源。正在进行的试验将阐明单独使用这些药物或与传统化疗药物联合使用的最有效策略。