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临床试验/NCT07274709
NCT07274709已完成不适用

Emulation of the MONALEESA-2 Trial Using Specialty Oncology Electronic Health Records Databases

Shirley Vichy Wang1 个研究点 分布在 1 个国家目标入组 2,495 人开始时间: 2025年9月7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
发起方
入组人数
2,495
试验地点
1
主要终点
Time to all-cause mortality/overall survival (OS)

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 MONALEESA-2 trial. MONALEESA-2 was a Phase III, double-blind, randomized study assessing the efficacy and safety of ribociclib (600 mg orally once daily on days 1-21 of a 28-day cycle, followed by 7 days off) in combination with letrozole (2.5 mg orally once daily, continuously) versus letrozole alone in postmenopausal women with hormone receptor-positive [estrogen receptor (ER) and/or progesterone receptor (PR)], human epidermal growth factor receptor 2-negative (HER2-) advanced breast cancer who had not received prior systemic treatment for their advanced disease.

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

  • Study Period:
  • ENCORE database 1 (EDB1): Patient identification period: 01/01/2011-04/30/2024 with follow-up information through data cut-off date on 04/30/2024 ENCORE database 3 (EDB3): Follow-up information through June 2023 (there is no specific time period restrictions for patient eligibility) ENCORE database 4 (EDB4): Patient identification period: 10/01/2018-09/30/2023 with follow-up information through data cut-off date on 09/30/
  • Inclusion Criteria:
  • Age ≥18 years through 2017 to 2023
  • Metastatic breast cancer
  • Hormone receptor positive (ER/PR+)
  • Untreated with systemic anticancer therapy for advanced disease
  • ECOG performance status of 0 or 1
  • HER2-negative

排除标准

  • Prior treatment with CDK4/6 inhibitor
  • Locally advanced (unresectable) or inflammatory breast cancer
  • Non-breast cancer malignancy other than basal/squamous cell skin cancer or carcinoma in situ of cervix
  • Prior adjuvant therapy for breast cancer
  • Systemic anticancer therapy other than ribociclib or letrozole

研究组 & 干预措施

Initiation of ribociclib plus letrozole

Exposure group

干预措施: Initiation of ribociclib (Drug)

Initiation of letrozole

Reference group

干预措施: Initiation of ribociclib (Drug)

Initiation of letrozole

Reference group

干预措施: Initiation of letrozole (Drug)

结局指标

主要结局

Time to all-cause mortality/overall survival (OS)

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

未报告次要终点

研究者

发起方
Shirley Vichy Wang
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Shirley Vichy Wang

Associate Professor

Brigham and Women's Hospital

研究点 (1)

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