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Completed

NCT Number: NCT07225790

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

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.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Brigham and Women's Hospital

Boston, Massachusetts, 02120, United States

About this study

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.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

Initiation of abemaciclib plus letrozole/anastrozole

Drug

Any doses and frequency observed in clinical practice will be allowed

Initiation of letrozole/anastrozole

Drug

Any doses and frequency observed in clinical practice will be allowed

Primary outcomes

  1. Time to all-cause mortality (overall survival)

    Time frame: 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)

Secondary outcomes

  1. Time to next treatment (TTNT)

    Time frame: 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)

    Hazard ratio (95% CI)

Sponsors and collaborators

Lead sponsor

Brigham and Women's Hospital

Other

Collaborators

  • Food and Drug Administration (FDA)

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Nov 10, 2025
Registry last updated
May 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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