CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 165 enrolled / 165 target
Drug / intervention
Blood samplingbiological
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/NCT05303129
NCT05303129N/ACompletedHigh Momentum (3.4/mo)Completion was 18mo ago

Prognostic Impact of the Neutrophil/Lymphocyte Ratio (NLR) in the Treatment of First-line Metastatic or Locally Advanced Breast Cancer Treated With CDK4/6 in

Centre Francois Baclesse·interventional·Posted Mar 31, 2022·Updated Jun 11, 2026

In Brief

A clinical study evaluating Blood sampling for Breast Cancer and Metastatic Breast Cancer. Completed, enrolled 165 participants across 2 sites.

Signals

Enrolling ahead of pace

Detailed Summary

The impact of the inflammatory microenvironment in predicting the benefit of a CDK4/6 inhibitor in the treatment of locally advanced or first line metastatic breast cancer has not yet been studied. We propose a multicenter prospective study to confirm the prognostic value of pre-therapy NLR on progression-free survival of patients initiating treatment with a CDK4/6 inhibitor combined with hormonal therapy for locally advanced or metastatic HR-pos / HER2-neg breast cancer. We will also evaluate other markers of inflammation and their prognostic and predictive value for a better response to CDK4/6 inhibitor therapy in combination with hormone therapy in these patients. Specific blood tests (lymphocyte typing) will be performed during treatment with CDK4/6.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance
Collaborators--

Timeline

N/ACompletedFinished
2023202420252026
First PostedMar 31, 2022
Enrollment StartMay 27, 2022
Primary CompletionDec 17, 2024
TodayJul 2, 2026
Enrollment to primary: 2.6 yearsPosted 4.3 years ago

Arms & Interventions

Blood testsother

Realization of 4 blood tests for Lymphocyte typing (Neutrophil/Lymphocyte ratio (NLR), CD4+ and CD8+ lymphocyte counts ), during CDK4/6 treatment : * before initiation of CDK4/6 treatment * At 3 mois after initiation of CDK4/6 treatment * At 6 mois after initiation of CDK4/6 treatment * At 12 mois after initiation of CDK4/6 treatment or at early end of study

Biological: Blood sampling

Interventions

Blood samplingbiological

Blood sampling for Lymphocyte typing (Neutrophil/Lymphocyte ratio (NLR), CD4+ and CD8+ lymphocyte counts )