挽救纳米颗粒白蛋白结合紫杉醇治疗复发性宫颈癌的安全性和有效性:可行性研究。

Gynecologic oncology research and practice Pub Date : 2016-04-14 eCollection Date: 2016-01-01 DOI:10.1186/s40661-016-0025-6
Lindsey E Minion, Dana M Chase, John H Farley, Lyndsay J Willmott, Bradley J Monk
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引用次数: 9

摘要

背景:在铂和紫杉烷化疗后,无论是否使用贝伐单抗,晚期或复发宫颈癌都缺乏有效的治疗方案。我们的目的是回顾单一机构在纳米颗粒白蛋白结合(NAB)紫杉醇联合或不联合贝伐单抗治疗复发性难治性宫颈癌方面的经验。方法:根据圣约瑟夫医院和医疗中心机构审查委员会制定的规定,进行回顾性病例系列研究。我们回顾了亚利桑那大学癌症中心门诊输液中心的化疗记录,以确定2011年11月至2015年2月期间接受nab -紫杉醇治疗的所有晚期宫颈癌患者。从患者图表中提取以下数据点:人口统计信息、周期数、无进展生存期(PFS)、总生存期(OS)、剂量减少和剂量限制性毒性。此外,还计算了平均治疗周期数和复发年龄。结果:12例患者接受nab -紫杉醇治疗。平均复发年龄为47.2岁(36-55岁)。9例为鳞状细胞组织学,3例为腺癌组织学。所有受试者均以铂和紫杉烷或铂和拓扑替康化疗失败。两名受试者失去随访机会。nab -紫杉醇的中位周期数为6.5(2-19)。研究人群中nab -紫杉醇的总周期数为65。7名受试者与贝伐单抗联合治疗。其中,3名受试者仍然活着,1名受试者目前正在接受nab -紫杉醇的积极治疗。所有达到死亡终点的受试者的中位PFS和OS分别为4.8个月和8.9个月(n = 7)。1名受试者因周围神经病变停用了nab -紫杉醇,1名受试者在接受nab -紫杉醇和贝伐单抗联合治疗时出现膀胱阴道瘘。结论:nab -紫杉醇联合或不联合贝伐单抗治疗复发性宫颈癌在铂紫杉醇或拓扑替康化疗失败后是可耐受的,并且具有潜在的活性。这个小病例系列值得通过前瞻性临床试验来证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Safety and efficacy of salvage nano-particle albumin bound paclitaxel in recurrent cervical cancer: a feasibility study.

Safety and efficacy of salvage nano-particle albumin bound paclitaxel in recurrent cervical cancer: a feasibility study.

Safety and efficacy of salvage nano-particle albumin bound paclitaxel in recurrent cervical cancer: a feasibility study.

Background: After platinum and taxane chemotherapy, with or without bevacizumab, active regimens for advanced or recurrent cervical cancer are lacking. Our objective was to review a single institution experience in treating recurrent, refractory cervical cancer with nano-particle albumin bound (NAB) paclitaxel with or without bevacizumab.

Methods: This retrospective case series was conducted in accordance with the regulations set forth by the Institutional Review Board at St. Joseph's Hospital and Medical center. The chemotherapy log at the outpatient infusion center at the University of Arizona Cancer Center was reviewed to identify all advanced cervical cancer patients treated with NAB-paclitaxel from November 2011 until February 2015. The following data points were extracted from patient charts: demographic information, number of cycles, progression free survival (PFS), overall survival (OS), dose reductions and dose-limiting toxicities. In addition the average number of treatment cycles and age at recurrence were calculated.

Results: A total of 12 subjects were identified as receiving treatment with NAB-paclitaxel. Mean age at time of recurrence was 47.2 years (36-55). Nine subjects had squamous cell histology and three subjects had adenocarcinoma histology. All subjects had failed treatment with platinum and taxane, or platinum and topotecan chemotherapy. Two subjects were lost to follow up. The Median number of cycles of NAB-paclitaxel was 6.5 (2-19). The total number of cycles of NAB-paclitaxel in the study population was 65. Seven subjects were treated in combination with bevacizumab. Of these, three subjects are still alive and one subject is currently receiving active treatment with NAB-paclitaxel. The median PFS and OS for all subjects that met mortality endpoint was 4.8 months and 8.9 months (n = 7), respectively. One subject discontinued NAB-paclitaxel secondary to peripheral neuropathy, and one subject developed a vesicovaginal fistula while obtaining combination NAB-paclitaxel and bevacizumab therapy.

Conclusions: NAB-paclitaxel with or without bevacizumab is tolerable and potentially active in treating recurrent cervical cancer after failing platinum-taxane or topotecan chemotherapy. This small case series deserves confirmation through prospective clinical trials.

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