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临床试验/NCT07225790
NCT07225790已完成不适用

Emulation of the MONARCH-3 Trial Using Specialty Oncology Electronic Health Records Databases

Brigham and Women's Hospital2 个研究点 分布在 1 个国家目标入组 3,883 人开始时间: 2025年11月3日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
3,883
试验地点
2
主要终点
Time to all-cause mortality (overall survival)

研究概览

简要总结

Investigators are building an empirical evidence base for real world data through large-scale emulation of randomized controlled trials. The investigators' goal is to understand for what types of clinical questions real world data analyses can be conducted with confidence and how to implement such studies.

详细描述

Randomized controlled trials (RCTs) are generally regarded as the gold-standard of evidence for establishing efficacy of medical products. However, real-world data (RWD) are increasingly used to complement evidence from RCTs. Yet, to have confidence in the accuracy of non-interventional studies medical products and their outcomes in oncology, investigators need to know what questions can be validly answered, with which non-interventional study designs, and which analysis methods are appropriate, given the data that is available. Building on a process from the RCT DUPLICATE initiative1-4 EmulatioN of Comparative Oncology trials with Real-world Evidence (ENCORE) is part of the expansion project specific to oncology and aims to emulate 12 randomized oncology RCTs using multiple EHR data sources.

The purpose of this protocol is to describe the emulation of the MONARCH-3 trial. MONARCH 3 is a double-blind, randomized phase III study of abemaciclib or placebo plus a nonsteroidal aromatase inhibitor in 493 postmenopausal women with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced breast cancer who had no prior systemic therapy in the advanced setting. Patients received abemaciclib or placebo (150 mg twice daily continuous schedule) plus either 1 mg anastrozole or 2.5 mg letrozole/anastrozole, daily.

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

  • Female aged ≥18 years at treatment initiation from 2017 - 2023
  • Evidence of metastatic breast cancer (MBC)
  • Documentation of Estrogen/Progesterone receptor-positive (ER/PR+)
  • Documentation of Human Epidermal Growth Factor Receptor Negative (HER2-)
  • ECOG performance status of 0 or 1 within 90 days of index date

排除标准

  • CNS metastases
  • Prior treatment with CKD4/6 inhibitor
  • Prior or current treatment with chemotherapy or endocrine therapy other than letrozole/anastrozole for systemic anticancer therapy for MBC.
  • Prior (neo-)adjuvant endocrine therapy
  • Systemic anticancer therapy other than abemaciclib or letrozole/anastrozole
  • Non-breast cancer malignancy other than basal/squamous cell skin cancer or carcinoma in situ of cervix

研究组 & 干预措施

Initiation of abemaciclib plus letrozole/anastrozole

Any doses and frequency observed in clinical practice will be allowed

干预措施: Initiation of abemaciclib plus letrozole/anastrozole (Drug)

Initiation of letrozole/anastrozole

Any doses and frequency observed in clinical practice will be allowed

干预措施: Initiation of letrozole/anastrozole (Drug)

结局指标

主要结局

Time to all-cause mortality (overall survival)

时间窗: From time of initiation of therapy through the earliest of death from any cause (the primary outcome of interest) or end of data availability (depending on specialty oncology registry data provider, end of data ranges from June 2023 to April 2024)

Hazard ratio (95% CI)

次要结局

  • Time to next treatment (TTNT)(From time of initiation of therapy through the earliest of TTNT, death from any cause, or end of data availability (depending on specialty oncology registry data provider, end of data ranges from June 2023 to April 2024))

研究者

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

Shirley Vichy Wang

Associate Professor

Brigham and Women's Hospital

研究点 (2)

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