首页> 外文OA文献 >The clinical benefit of pegylated liposomal doxorubicin in patients with metastatic breast cancer previously treated with conventional anthracyclines: a multicentre phase II trial
【2h】

The clinical benefit of pegylated liposomal doxorubicin in patients with metastatic breast cancer previously treated with conventional anthracyclines: a multicentre phase II trial

机译:聚乙二醇脂质体阿霉素对先前用常规蒽环类药物治疗的转移性乳腺癌患者的临床益处:一项多中心II期试验

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

This study evaluates the clinical benefit of pegylated liposomal doxorubicin (PLD) in patients with metastatic breast cancer (MBC), previously treated with conventional anthracyclines. Seventy-nine women with MBC previously treated with anthracyclines received PLD 50 mg m−2 every 4 weeks. All patients were previously treated with chemotherapy and 30% of patients had ⩾3 prior chemotherapies for metastatic disease. Patients were considered anthracycline resistant when they had disease progression on anthracycline therapy for MBC or within 6 months of adjuvant therapy. The overall clinical benefit rate (objective response+stable disease ⩾24 weeks) was 24% (16.1% in patients with documented anthracycline resistance vs 29% in patients classified as having non-anthracycline-resistant disease). There was no difference with respect to the clinical benefit between patients who received PLD >12 months and those who received PLD ⩽12 months since last anthracycline treatment for metastatic disease (clinical benefit 25 vs 24.1%, respectively). Median time to progression and overall survival were 3.6 and 12.3 months, respectively. The median duration of response was 12 months, and the median time to progression in patients with stable disease (any) was 9.5 months. Fourteen patients (17.7%) had a prolonged clinical benefit lasting ⩾12 months. In conclusion, PLD was associated with an evident clinical benefit in anthracycline-pretreated patients with MBC.
机译:这项研究评估了聚乙二醇脂质体阿霉素(PLD)在先前用常规蒽环类药物治疗的转移性乳腺癌(MBC)患者中的临床获益。先前接受蒽环类药物治疗的79例MBC妇女每4周接受PLD50μmgm-2。所有患者先前均接受过化学疗法治疗,其中30%的患者已接受过⩾3的转移性化疗。当患者接受MBC蒽环类药物治疗或在辅助治疗后6个月内疾病进展,则认为患者对蒽环类药物耐药。总体临床受益率(客观反应+稳定的疾病≥24周)为24%(已记录蒽环类耐药的患者为16.1%,非蒽环类耐药的患者为29%)。自上次蒽环类药物治疗转移性疾病以来接受PLD> 12个月的患者和接受PLD≥12个月的患者之间的临床获益无差异(分别为25%和24.1%的临床获益)。进展中位时间和总生存期分别为3.6和12.3个月。中位缓解期为12个月,而疾病稳定(任何)的患者中位进展时间为9.5个月。 14名患者(17.7%)的临床获益延长了12个月。总之,在蒽环类药物预处理的MBC患者中,PLD与明显的临床获益相关。

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