...
首页> 外文期刊>Breast cancer >Factors associated with prolonged overall survival in patients with postmenopausal estrogen receptor-positive advanced breast cancer using real-world data: a follow-up analysis of the JBCRG-C06 Safari study
【24h】

Factors associated with prolonged overall survival in patients with postmenopausal estrogen receptor-positive advanced breast cancer using real-world data: a follow-up analysis of the JBCRG-C06 Safari study

机译:使用现实数据的绝经后雌激素受体阳性晚期乳腺癌患者长期全身生存的因素:JBCRG-C06 Safari研究的后续分析

获取原文

摘要

Background Assessing survival risk is important for discussing treatment options with estrogen receptor-positive (ER+) advanced breast cancer (ABC) patients. However, there are few reports from large-scale databases on the survival risk factors in ER+ ABC. The Safari study (UMIN000015168) was a retrospective, multicenter cohort study involving 1072 Japanese patients receiving fulvestrant 500?mg mostly as a second- or later-line endocrine therapy for ER+ ABC. The follow-up data after the Safari study were examined, focusing on any relationship between clinicopathological factors and overall survival (OS) in ER+ ABC patients. Methods OS in patients with ER+ ABC was analyzed by univariate and multivariate analyses with a Cox proportional hazards model in this study. Results A total of 1031 cases were evaluable for OS analysis. Multivariate analysis showed that younger age (
机译:背景技术评估生存风险对于讨论雌激素受体阳性(ER +)晚期乳腺癌(ABC)患者的治疗方案非常重要。但是,来自ER + ABC的生存风险因素的大规模数据库中很少有报道。野生动物园(UMIN0015168)是一种回顾性的多中心队列研究,涉及1072名日本患者接受氟斯特朗500岁的患者,主要是ER + ABC的第二次或后期内分泌疗法。检查野生动物园研究后的后续数据,专注于ER + ABC患者的临床病理因子和整体存活之间的任何关系。方法通过本研究中的Cox比例危险模型进行单变量和多变量分析,分析了ER + ABC患者的OS。结果OS分析总共评价1031例。多变量分析表明,年轻的年龄(<?60?年),从ABC诊断到氟斯特语(≥?3?年),没有先前的姑息治疗,并且孕酮受体(PGR)消极(PGRα)的持久性化疗与延长OS(中位数7.0?年)显着相关。对于组织学或核等级数据的病例,较低的组织学或核等级也与较长的操作系统相关。在复发转移病例中,长无病间隔(DFI)与较长的OS不相关。结论在ER + ABC患者的治疗历史包括氟斯特语,较年轻,从ABC诊断到氟斯特语的较长时间,没有先前的姑息化疗使用,PGRα,较低的组织学或核等级与延长的OS呈正相关。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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