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Development of a platform for systemic antiangiogenesis therapy for advanced cervical cancer

机译:晚期宫颈癌全身抗血管生成治疗平台的开发

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Women with metastatic, recurrent, or persistent cervical carcinoma historically have had extremely limited treatment options. Systemic chemotherapy in these settings is predominantly palliative and has been associated with platinum resistance, nondurable responses, rapid progression of disease with deterioration in quality of life, and early death. At the cooperative group level, efforts to breach this clinical impasse have focused on incorporation of antiangiogenesis therapy, medical optimization, and identification of less toxic regimens. Gynecologic Oncology Group protocols 204 and 240, along with the Japanese Clinical Oncology Group protocol 0505, make up the pivotal phase 3 clinical trials that have provided 3 distinct treatment options. These options incorporate the antiangiogenesis humanized monoclonal antibody bevacizumab in combination with either a platinum-based or nonplatinum-based chemotherapy doublet. This review will highlight the development of bevacizumab in advanced cervical cancer and address the relevance of the survival gain obtained using antiangiogenesis therapy in this high-risk population.
机译:历史上,患有转移性,复发性或持续性宫颈癌的妇女的治疗选择极为有限。在这些情况下,全身化疗主要为姑息性治疗,与铂耐药性,不持久的反应,疾病进展迅速,生活质量下降和早期死亡有关。在合作小组的层面上,为打破这种临床僵局而进行的努力主要集中在抗血管生成治疗,药物优化和毒性较低的治疗方案的确定上。妇科肿瘤学组规程204和240,以及日本临床肿瘤学组规程0505,共同构成了关键的3期临床试验,提供了3种不同的治疗选择。这些选择将抗血管生成人源化单克隆抗体贝伐单抗与铂基或非铂基化学双链体组合使用。这篇综述将着重介绍贝伐单抗在晚期宫颈癌中的发展,并探讨在这一高风险人群中使用抗血管生成疗法获得的生存增益的相关性。

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