Trials / Recruiting
RecruitingNCT06880029
Circadian Rhythm Impact on TNBC Response to Neoadjuvant Immunotherapy
Circadian Rhythm Impact on Triple Negative Breast Cancer Response to Neoadjuvant Immunotherapy - a Feasibility Randomized Trial
- Status
- Recruiting
- Phase
- Phase 1 / Phase 2
- Study type
- Interventional
- Enrollment
- 20 (estimated)
- Sponsor
- Centro Hospitalar de Vila Nova de Gaia/Espinho, E.P.E. · Other Government
- Sex
- Female
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
CIRCADIAN is a prospective randomized clinical trial designed to evaluate the impact of pembrolizumab infusions' time-of-day on pathological complete response (pCR) rate among TNBC patients undergoing neoadjuvant treatment.
Detailed description
Patients will be randomized 1:1 to receive all neoadjuvant pembrolizumab cycles (400 mg every 6 weeks) before versus after noon. Subjects will be stratified based on clinical stage at diagnosis (St. II vs III). Primary outcome will be pCR rate. As a secondary outcome, we will assess for treatment related toxicity. For planned exploratory circadian rhythm evaluation, daily body temperature and salivary cortisol variation will be measured before each ICI infusion and the Munich Chronotype Questionnaire (MCTQ) will be applied. To assess for emotional stress, physical exercise habits, stimulating substances use and light exposure, patients will also be subjected to the Distress Thermometer and a lifestyle questionnaire. For planned exploratory biomarker research, tumor infiltrating lymphocytes (TILs) analysis will be performed on the initial diagnostic biopsy and after surgery, on residual tumor (in patients not achieving pCR). Cytokine quantification and bulk RNA sequencing plus flow cytometry studies for immune populations profiling will be performed on peripheral blood, at baseline and before surgery, to check for potential biomarkers of circadian modulation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Morning pembrolizumab infusions | Patients will be randomized 1:1 to receive all three neoadjuvant pembrolizumab cycles in the morning (before noon) or in the afternoon (after noon). |
Timeline
- Start date
- 2024-09-01
- Primary completion
- 2025-09-01
- Completion
- 2025-09-01
- First posted
- 2025-03-17
- Last updated
- 2025-03-19
Locations
1 site across 1 country: Portugal
Source: ClinicalTrials.gov record NCT06880029. Inclusion in this directory is not an endorsement.