首页> 美国卫生研究院文献>Current Oncology >First-Line Treatment with a Cyclin-Dependent Kinase 4/6 Inhibitor Plus an Aromatase Inhibitor for Metastatic Breast Cancer in Alberta
【2h】

First-Line Treatment with a Cyclin-Dependent Kinase 4/6 Inhibitor Plus an Aromatase Inhibitor for Metastatic Breast Cancer in Alberta

机译:用细胞周期蛋白依赖性激酶4/6抑制剂加上亚伯塔省转移性乳腺癌的芳香酶抑制剂的一线治疗

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

In this analysis, we describe population-based outcomes for first-line treatment with a cyclin-dependent kinase 4/6 inhibitor (CDK4/6i) combined with an aromatase inhibitor (AI). All patients who were prescribed CDK4/6i + AI from January 2016 through June 2019 were included. Patient demographics, tumour and treatment characteristics were collected and described. Survival distributions were estimated using the Kaplan–Meier method. Multivariate analysis (MVA) was constructed to examine associations between potentially prognostic clinical variables and progression-free survival (PFS). In total, 316 patients were included. The median age was 61 years. After a median follow-up of 28.1 months, the median PFS was 37.9 months (95% CI, 26.7–NR). In the MVA, PR-negative tumour (HR, 2.37; 95% CI, 1.45–3.88; p = 0.001) and CDK4/6i dose reduction (HR, 1.51; 95% CI, 1.06–2.16; p = 0.022) predicted worse PFS. Median overall survival (OS) was not reached. The 30-month and 36-month OS rates were 74% and 68%, respectively. Of patients who progressed, 89% received second-line treatment. Median time to progression on second-line chemotherapy was 9.0 (5.8–17.6) months, and median time to progression on second-line hormonal therapy +/− targeted agent was 4.0 (3.4–8.6) months (p = 0.012). CDK4/6i + AI as first-line treatment for HR-positive, HER2-negative MBC in Alberta is justified based on favourable PFS and early OS outcomes.
机译:在该分析中,我们描述了用细胞周期蛋白依赖性激酶4/6抑制剂(CDK4 / 6i)与芳香酶抑制剂(AI)结合的群体的群体结果。包括从2016年1月到2019年6月订明CDK4 / 6I + AI的所有患者。收集和描述患者人口统计学,肿瘤和治疗特征。使用Kaplan-Meier方法估计生存分布。构建多变量分析(MVA)以检查潜在预后临床变量和无进展存活(PFS)之间的关联。总共包括316名患者。中位年龄为61岁。经过28.1个月的中位随访后,中位数PFS为37.9个月(95%CI,26.7-NR)。在MVA,PR阴性肿瘤(HR,2.37; 95%CI,1.45-3.88; P = 0.001)和CDK4 / 6i剂量还原(HR,1.51; 95%CI,1.06-2.16; P = 0.022)预测更糟PFS。没有达到中位数总生存(OS)。 30个月和36个月的OS率分别为74%和68%。患者的进展,89%接受了二线治疗。二线化疗的中位时间进行了9.0(5.8-17.6)个月,第二线激素治疗+/-靶向剂上的中位数时间为4.0(3.4-8.6)个月(P = 0.012)。 CDK4 / 6i + AI作为HR阳性的一线治疗,艾伯塔省的HER2阴性MBC基于有利的PFS和早期OS结果是合理的。

著录项

  • 期刊名称 Current Oncology
  • 作者单位
  • 年(卷),期 2021(28),3
  • 年度 2021
  • 页码 2270–2280
  • 总页数 11
  • 原文格式 PDF
  • 正文语种
  • 中图分类 肿瘤学;
  • 关键词

    机译:转移性乳腺癌;帕尔巴克测妇;ribociclib;现实世界;加拿大;中位时间进展二线治疗;

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