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晚期或复发性宫颈癌的治疗:化疗及其他方法。

Management of advanced or recurrent cervical cancer: chemotherapy and beyond.

机构信息

Department of Obstetrics and Gynecology, 699 Concession Street, McMaster University, Hamilton, ON, L9G 2Z8 Canada.

出版信息

Expert Rev Anticancer Ther. 2014 Mar;14(3):319-32. doi: 10.1586/14737140.2014.866041. Epub 2014 Jan 10.

Abstract

Metastatic or recurrent cervical cancer has a survival duration of approximately 12 months. Thus, we review the outcomes of chemotherapy and/or novel agents for women who present in this situation. Included were studies in women with advanced or recurrent cervical cancer where at least response rate, survival or toxicity were reported. Platinum alone chemotherapy at 50 mg/m(2) is superior to other single-agent platinum or nonplatinum regimens in terms of efficacy and toxicity profile. Platinum with either paclitaxel, gemcitibine, topotecan or vinorelbine has equivalent efficacy but differ with respect to toxicity profile and convenience of treatment regimen. Bevacizumab in addition to combination chemotherapy provides a duration of survival that is 3.7 months longer than that provided by combination chemotherapy alone. EGF receptor (EGFR) tyrosine kinase inhibitor agents did not provide promising efficacy. Bevacizumab in addition to combination chemotherapy provides superior efficacy with acceptable toxicity. Evaluation of other novel targeted antiangiogenic agents, either alone or in combination with chemotherapy is ongoing.

摘要

转移性或复发性宫颈癌的生存时间约为 12 个月。因此,我们回顾了针对这种情况的女性化疗和/或新型药物的治疗效果。纳入的研究对象为患有晚期或复发性宫颈癌的女性,这些研究至少报告了缓解率、生存率或毒性。在疗效和毒性特征方面,50mg/m(2)的顺铂单药化疗优于其他单药铂类或非铂类方案。顺铂联合紫杉醇、吉西他滨、拓扑替康或长春瑞滨的疗效相当,但毒性特征和治疗方案的便利性不同。贝伐珠单抗联合化疗可使患者的生存时间延长 3.7 个月。表皮生长因子受体(EGFR)酪氨酸激酶抑制剂药物并未提供有前景的疗效。贝伐珠单抗联合化疗具有较好的疗效且毒性可接受。正在评估其他新型靶向抗血管生成药物单独或联合化疗的疗效。

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