Determinants of the Response to BTK Degraders (BTKd) in Double Refractory Chronic Lymphocytic Leukemia (CLL)

Status: Recruiting
Location: See all (14) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY

The aim of the REBELLE cohort - bio-collection is to collect samples from patients with Chronic Lymphocytic Leukemia (CLL), to facilitate access for the National Institute of Health and Medical Research (INSERM) to patients with double-refractory CLL. To do this, an additional blood or bone marrow sample to those planned in the context of patient care or a residual lymph node biopsy sample will be collected after signing consent. These samples will first be sent to the Filothèque for temporary storage, and will then be transferred to CRCI²NA (Nantes - Angers Cancer and Immunology Research Center) for analysis with the aim of studying the mechanisms of resistance and response to BTK degraders (BTKd).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patient with confirmed double refractory CLL to both BTKi and BCL-2i, defined as:

‣ Any patient who has received both a BTKi and a BCL-2i, regardless of treatment regimen, and has shown clinical progression either during treatment with both BTKi and BCL-2i, or within 36 months after stopping BCL-2i.

⁃ Any patient identified with known biological resistance mutations to BTKi or BCL-2i, regardless of clinical progression.

• Patient who has provided informed consent to participate in the study.

• Patient covered by a social security health insurance plan

Locations
Other Locations
France
CHU de Angers
NOT_YET_RECRUITING
Angers
CHU de Bordeaux
NOT_YET_RECRUITING
Bordeaux
Institut Bergonié
NOT_YET_RECRUITING
Bordeaux
CHU de Clermont-Ferrand
NOT_YET_RECRUITING
Clermont-ferrand
CHD Vendée
NOT_YET_RECRUITING
La Roche-sur-yon
Centre Léon Bernard
NOT_YET_RECRUITING
Lyon
Institut Paoli-Calmettes (Marseille)
NOT_YET_RECRUITING
Marseille
CHU de Montpellier
NOT_YET_RECRUITING
Montpellier
CH Régional Universitaire de Nancy
NOT_YET_RECRUITING
Nancy
University Hospital
RECRUITING
Nantes
Hôpital Avicenne (AP-HP)
NOT_YET_RECRUITING
Paris
Hôpital Universitaire Pitié Salpêtrière de Paris
NOT_YET_RECRUITING
Paris
CHU de Poitiers
NOT_YET_RECRUITING
Poitiers
Centre Henri-Becquerel de Rouen
NOT_YET_RECRUITING
Rouen
Contact Information
Primary
ANNE LOK, MD, PhD
anne.lok@chu-nantes.fr
02. 53.48.28.36
Time Frame
Start Date: 2025-10-09
Estimated Completion Date: 2039-09-15
Participants
Target number of participants: 60
Treatments
double-refractory CLL patients
Collection of additional samples of blood and bone marrow or residual lymph node biopsy at the time of inclusion (for diagnosis or relapse) and relapse.
Sponsors
Leads: Nantes University Hospital

This content was sourced from clinicaltrials.gov