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临床试验/NCT04202328
NCT04202328Unknown不适用

A Retrospective Study for Evaluation of Real-world Efficacy and Safety of T-DM1 in HER2-positive Locally-advanced Unresectable or Metastatic Breast Cancer

Samsung Medical Center60 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2019年12月19日最近更新:
适应症

试验速览

阶段
不适用
入组人数
1,000
试验地点
60
主要终点
Incidence of adverse events

研究概览

简要总结

This is a retrospective, multicenter, non-interventional study for the evaluation of real-world efficacy and safety of T-DM1 in metastatic/relapsed HER2-positive breast cancer as part of the establishment of hospital medical record collection system to evaluate drug effectiveness by Health Insurance Review & Assessment Service (HIRA). The medical records in approximately 1,000 patients of HER2-positive locally-advanced unresectable or metastatic breast cancer, who have received Kadcyla(Trastuzumab Emtansine, T-DM1) previously, will be collected.

详细描述

T-DM1 therapy has shown a survival benefit in previously trastuzumab-treated HER2-positive locally-advanced unresectable or metastatic breast cancer patients from clinical trials. However, the real-world efficacy and safety of T-DM1 in KOREA were not evaluated outside the controlled clinical trials. Therefore, this large multicenter retrospective analysis was designed to evaluate the real-world efficacy and safety of T-DM1 under the Korea National Health Insurance System. The medical records in approximately 1,000 patients with relapsed or De Novo metastatic breast cancer, who have received T-DM1 between Aug 03, 2017 and Dec 31, 2018 will be collected. Eligibility criteria included age ≥ 19 years, histologically confirmed HER2-positive, relapsed after primary surgery or initially metastatic breast cancer, and previous trastuzumab treated. Efficacy was evaluated by overall survival, progression free survival, time to progression, objective response rate, disease control rate, duration of response and time to next treatment. Safety was evaluated by hematologic or non-non hematologic toxicities and adverse events of special interest with T-DM1 therapy.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Age ≥19 years at the time of study registration
  • Participants must have histologically confirmed HER2-positive breast cancer
  • Locally advanced unresectable or metastatic patients
  • Patients who have received T-DM1 therapy between Aug 2017 and December 2018 under the Korea National Health Insurance System

排除标准

  • Patients who have received T-DM1 therapy outside of the Korea National Health Insurance System

结局指标

主要结局

Incidence of adverse events

时间窗: Until September 30, 2019

Number (percentage) of subjects reporting adverse events

Progression free Survival, PFS

时间窗: Until September 30, 2019

Time from the start of T-DM1 to disease progression or death from any cause

次要结局

  • Time to Next Treatment, TTNT(Until September 30, 2019)
  • Disease Control Rate, DCR(Until September 30, 2019)
  • Adverse events of special interest(Until September 30, 2019)
  • Objective Response Rate, ORR(Until September 30, 2019)
  • Duration of response(Until September 30, 2019)
  • Overall Survival, OS(Until September 30, 2019)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Yeon Hee Park

Professor

Samsung Medical Center

研究点 (60)

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