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临床试验/NCT03676257
NCT03676257已完成不适用

Survival Endpoints for Treatment Evaluation in Subjects Treated for Metastatic Breast Cancer: Contribution of Real-life Databases

Institut Bergonié1 个研究点 分布在 1 个国家目标入组 20,033 人开始时间: 2008年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
20,033
试验地点
1
主要终点
Overall Survival (OS) for Commonly Prescribed First-line Treatment Strategies

研究概览

简要总结

Overall survival (OS) is considered the most reliable cancer endpoint and used by the Health Rregulatory authorities (HRA). OS presents multiple advantages in cancer randomized controlled trials (RCT): it is universally accepted as a measure of clinical benefit for the patient; it is objectively defined, both in terms of events and date of incidence; it is easily and precisely measured and thus reproducible; it can be exhaustively collected. As such, OS has been validated by HRAs. On the other hand, OS presents some limitations. Observing a benefit on OS may require a large number of patients and/or considerable time for patient follow-up. Costs for trials may be increased, and there might be delays in the introduction of possible beneficial treatments for patients. The development of alternative endpoints that could capture treatment benefit appropriately and be measurable earlier, is central for the evolution of clinical research in oncology.

Real world data (RWD) are defined as other sources than clinical trials such as: electronic medical records, registries, insurance claims, pharmacy records, death certificates and other patient-generated data.

This research is aimed at (i) describing the existing endpoints of survival in real-life setting, (ii) comparing the correlation at individual level with data to clinical trials for related to anti-HER2 targeted therapies and endocrine therapies in MBC. We will investigate the individual correlation between candidate surrogate endpoints and overall survival in a population-based record-computerized database centralizing data on about 20,000 patients from 2008 to 2017 in France.

This work should lead to the estimation of various time-to event endpoints (e.g. OS, PFS, etc), in the real-life setting, for mBC patients. In addition, we will estimate their individual correlation with OS, which should help us highlight potential surrogate endpoints in this setting. We will focuss on three distinct population, accounting for a large population of mBS patients: : patients treated with anti-HER2 targeted agents, patients treated with endocrine therapies and elderly population.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Women with a diagnosis of HR+ /HER2- metastatic breast cancer (mBC)

Women with a diagnosis of HR+ /HER2- metastatic breast cancer (mBC)

干预措施: Chemotherapy (exclusive) (Drug)

Women with a diagnosis of HR+ /HER2- metastatic breast cancer (mBC)

Women with a diagnosis of HR+ /HER2- metastatic breast cancer (mBC)

干预措施: Endocrine therapy (exclusive) (Drug)

Women with a diagnosis of HR+ /HER2- metastatic breast cancer (mBC)

Women with a diagnosis of HR+ /HER2- metastatic breast cancer (mBC)

干预措施: Combination of endocrine therapy and chemotherapy (Drug)

Women with a diagnosis of HR+ /HER2- metastatic breast cancer (mBC)

Women with a diagnosis of HR+ /HER2- metastatic breast cancer (mBC)

干预措施: Chemotherapy and targeted treatment (Drug)

Women with a diagnosis of HR+ /HER2- metastatic breast cancer (mBC)

Women with a diagnosis of HR+ /HER2- metastatic breast cancer (mBC)

干预措施: Combination of endocrine therapy and targeted treatment (Drug)

Women with a diagnosis of HR+ /HER2- metastatic breast cancer (mBC)

Women with a diagnosis of HR+ /HER2- metastatic breast cancer (mBC)

干预措施: Combination of chemotherapy, endocrine therapy and targeted treatment (Drug)

Women with a diagnosis of HR- /HER2- metastatic breast cancer (mBC)

Women with a diagnosis of HR- /HER2- metastatic breast cancer (mBC)

干预措施: Chemotherapy (exclusive) (Drug)

Women with a diagnosis of HR- /HER2- metastatic breast cancer (mBC)

Women with a diagnosis of HR- /HER2- metastatic breast cancer (mBC)

干预措施: Chemotherapy and targeted treatment (Drug)

Women with a diagnosis of HR+ /HER2+ metastatic breast cancer (mBC)

Women with a diagnosis of HR+ /HER2+ metastatic breast cancer (mBC)

干预措施: Chemotherapy (exclusive) (Drug)

Women with a diagnosis of HR+ /HER2+ metastatic breast cancer (mBC)

Women with a diagnosis of HR+ /HER2+ metastatic breast cancer (mBC)

干预措施: Endocrine therapy (exclusive) (Drug)

Women with a diagnosis of HR+ /HER2+ metastatic breast cancer (mBC)

Women with a diagnosis of HR+ /HER2+ metastatic breast cancer (mBC)

干预措施: Combination of endocrine therapy and chemotherapy (Drug)

Women with a diagnosis of HR+ /HER2+ metastatic breast cancer (mBC)

Women with a diagnosis of HR+ /HER2+ metastatic breast cancer (mBC)

干预措施: Chemotherapy and targeted treatment (Drug)

Women with a diagnosis of HR+ /HER2+ metastatic breast cancer (mBC)

Women with a diagnosis of HR+ /HER2+ metastatic breast cancer (mBC)

干预措施: Combination of endocrine therapy and targeted treatment (Drug)

Women with a diagnosis of HR+ /HER2+ metastatic breast cancer (mBC)

Women with a diagnosis of HR+ /HER2+ metastatic breast cancer (mBC)

干预措施: Combination of chemotherapy, endocrine therapy and targeted treatment (Drug)

Women with a diagnosis of HR- /HER2+ metastatic breast cancer (mBC)

Women with a diagnosis of HR- /HER2+ metastatic breast cancer (mBC)

干预措施: Chemotherapy (exclusive) (Drug)

Women with a diagnosis of HR- /HER2+ metastatic breast cancer (mBC)

Women with a diagnosis of HR- /HER2+ metastatic breast cancer (mBC)

干预措施: Chemotherapy and targeted treatment (Drug)

结局指标

主要结局

Overall Survival (OS) for Commonly Prescribed First-line Treatment Strategies

时间窗: 10 years

OS was defined as the time from diagnosis of mBC to the date of death from any cause.

次要结局

  • Real-world Progression-free Survival (rwPFS) for Commonly Prescribed First-line Treatment Strategies(10 years)
  • Association Between Overall Survival and Real-world Progression-free Survival for Commonly Prescribed First-line Treatment Strategies(10 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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