CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 20,033 enrolled
Drug / intervention
Chemotherapy (exclusive) +5 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03676257
NCT03676257N/ACompleted

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

Institut Bergonié·observational·Posted Sep 18, 2018·Updated Dec 10, 2025

In Brief

An observational study evaluating Chemotherapy (exclusive), Endocrine therapy (exclusive), and 4 other interventions for Metastatic Breast Cancer. Completed, enrolled 20,033 participants across 1 site.

Detailed Summary

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.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesFrance

Timeline

N/ACompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedSep 18, 2018
Enrollment StartJan 1, 2008
Primary CompletionDec 1, 2023
TodayJul 2, 2026
Enrollment to primary: 15.9 yearsPosted 7.8 years ago

Interventions

Chemotherapy (exclusive)drug

Administration of any chemotherapeutic agent(s)

Endocrine therapy (exclusive)drug

Administration of any type of endocrine therapy

Combination of endocrine therapy and chemotherapydrug

Any combination of endocrine therapy and chemotherapy

Chemotherapy and targeted treatmentdrug

Any combination of chemotherapy and targeted treatment(s)

Combination of endocrine therapy and targeted treatmentdrug

Any combination of endocrine therapy and targeted treatment

Combination of chemotherapy, endocrine therapy and targeted treatmentdrug

Any combination of chemotherapy, endocrine therapy and targeted treatment(s)