首页> 美国卫生研究院文献>Cancer Medicine >Efficacy of topotecan in pretreated metastatic poorly differentiated extrapulmonary neuroendocrine carcinoma
【2h】

Efficacy of topotecan in pretreated metastatic poorly differentiated extrapulmonary neuroendocrine carcinoma

机译:拓扑替康在预处理的转移性低分化肺外神经内分泌癌中的疗效

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Therapeutic options for metastatic poorly differentiated neuroendocrine carcinoma (NEC) after prior platinum‐based chemotherapy are limited. Topotecan is an approved second‐line chemotherapy for small cell lung cancer (SCLC). NEC is often considered to show a biological behavior similar to SCLC. The aim of this study was to analyze the efficacy of topotecan in pretreated metastatic NEC patients. We performed a retrospective analysis of all patients treated with topotecan for metastatic NEC who presented at our center between January 2005 and December 2014 (n = 30). All 30 patients had received at least a platinum and etoposide containing regimen as prior chemotherapy. Median proliferation rate (Ki67) was 80%. As best response to topotecan five patients showed a stable disease, two patients a partial remission, resulting in a disease control rate of 23%. Of the remaining 23 patients, 14 (47%) showed a progressive disease, nine (30%) died before radiologic response could be evaluated. Median progression‐free (PFS) and overall survival (OS) after start of topotecan was 2.1 and 4.1 months, respectively. In the subgroup analysis, patients with unknown primary (vs. those with a known primary) showed a significantly prolonged PFS of 3.5 months (vs. 1.9, P = 0.0107) and OS of 6.7 months (vs. 2.6 months, P = 0.0168). Grade 3/4 hematotoxicity was observed in 60% of patients. Topotecan shows only moderate antitumor activity in metastatic NEC. Disease control rate is lower than reported for SCLC. However, antitumor activity of topotecan seems higher in patients with unknown primary.
机译:先前基于铂的化疗后,转移性低分化神经内分泌癌(NEC)的治疗选择有限。托泊替康是一种批准用于小细胞肺癌(SCLC)的二线化疗。 NEC通常被认为具有类似于SCLC的生物学行为。这项研究的目的是分析拓扑替康在预处理的转移性NEC患者中的疗效。我们对2005年1月至2014年12月间在我们中心就诊的所有接受拓扑替康治疗转移性NEC的患者进行了回顾性分析(n = 30)。所有30例患者均已接受至少含铂和依托泊苷的化疗方案。中值增殖率(Ki67)为80%。由于对拓扑替康的最佳反应显示5例患者病情稳定,2例患者部分缓解,导致疾病控制率为23%。在其余的23名患者中,有14名(47%)表现为进行性疾病,其中9名(30%)在评估放射学反应之前死亡。拓扑替康开始后的无进展中位数(PFS)和总体生存期(OS)分别为2.1个月和4.1个月。在亚组分析中,原发性未知的患者(相对于原发性已知的患者)的PFS显着延长了3.5个月(vs.1.9,P = 0.0107),OS延长了6.7个月(vs.2.6个月,P = 0.0168) 。在60%的患者中观察到3/4级血液毒性。托泊替康在转移性NEC中仅显示中度抗肿瘤活性。疾病控制率低于报告的SCLC。但是,拓扑替康的抗肿瘤活性似乎在原发性未知的患者中更高。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号