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上皮性卵巢癌一线及二线治疗中靶向治疗作为维持治疗的当前作用综述;基于已完成的试验。

Review of the current role of targeted therapies as maintenance therapies in first and second line treatment of epithelial ovarian cancer; In the light of completed trials.

作者信息

Korkmaz Taner, Seber Selcuk, Basaran Gul

机构信息

Acibadem University Hospital, Turkey.

Namik Kemal University Hospital, Turkey.

出版信息

Crit Rev Oncol Hematol. 2016 Feb;98:180-8. doi: 10.1016/j.critrevonc.2015.10.006. Epub 2015 Nov 10.

Abstract

Late and recurrent stage ovarian cancer has a high mortality and low response rate to therapy beyond first line treatment. Although first line platinum/taxane based regimens have a satisfactory response rate eventually in most cases disease recurrence is common and second-line treatments are not curative. Delaying progression or recurrence is the main goal of current ongoing clinical studies by means of establishing an effective maintenance regimen with acceptable toxicity profile. Clearly, the persistence of dormant and drug-resistant cells after front-line treatments results in the inability to cure the disease. Over the past several years, the idea of prolongation of therapy for ovarian cancer has garnered clinical attention and academic debate. As a result of a greater understanding of the molecular pathways involved in carcinogenesis and tumor growth, a large number of potential therapeutic targets have been identified and drugs to block receptors, ligands or pathways are being developed. Currently, numerous clinical trials with targeted agents have just been completed or are ongoing involving patients achieving a complete or durable response after first-line and beyond the first line chemotherapy in order to evaluate the efficacy of different therapeutic approaches in terms of progression-free survival and overall survival.

摘要

晚期和复发性卵巢癌死亡率高,一线治疗后的后续治疗反应率低。尽管一线铂类/紫杉烷类方案最终在大多数情况下有令人满意的反应率,但疾病复发很常见,二线治疗无法治愈。通过建立具有可接受毒性特征的有效维持方案来延迟疾病进展或复发是当前正在进行的临床研究的主要目标。显然,一线治疗后休眠和耐药细胞的持续存在导致无法治愈该疾病。在过去几年中,延长卵巢癌治疗时间的想法引起了临床关注和学术讨论。由于对参与致癌作用和肿瘤生长的分子途径有了更深入的了解,已确定了大量潜在的治疗靶点,并且正在开发阻断受体、配体或途径的药物。目前,许多针对靶向药物的临床试验刚刚完成或正在进行,涉及在一线及一线以上化疗后获得完全或持久反应的患者,以便根据无进展生存期和总生存期评估不同治疗方法的疗效。

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