RecruitingNCT05246345

Venetoclax Resistance Landscape in Chronic Lymphocytic Leukemia


Sponsor

University Hospital, Clermont-Ferrand

Enrollment

50 participants

Start Date

Mar 7, 2022

Study Type

OBSERVATIONAL

Conditions

Summary

The purpose of this study is to collect medical informations and samples from refractory and/or relapsed chronic lymphocytic leukemia during or after venetoclax treatment, in order to evaluate the frequency of resistance mechanisms.


Eligibility

Min Age: 18 Years

Inclusion Criteria7

  • Age greater than or equal to 18 years old;
  • chronic lymphocytic leukemia diagnosis according to iwCLL criteria;
  • refractory and/or relapsed disease during or after venetoclax treatment;
  • tumor samples available.
  • Relapse might be progressive chronic lymphocytic leukemia or transformation into Richter syndrome.
  • Patients must be able to express their opposition to be enrolled in this study, if need be.
  • Patients must be affiliated at the French Social Security system

Exclusion Criteria2

  • Patients of their legal guardians refusing to participate
  • \-

Locations(14)

CHU d'Amiens

Amiens, France

CHU de Besançon

Besançon, France

Hopital AVICENNE

Bobigny, France

CHU clermont-ferrand

Clermont-Ferrand, France

CHU de Clermont Ferrand

Clermont-Ferrand, France

CHU Grenoble

Grenoble, France

CHRU de Lille

Lille, France

Centre LEON BERARD

Lyon, France

CHU de Montpellier

Montpellier, France

CHU Nancy

Nancy, France

Hopital Pitié Salpetrière

Paris, France

Hopital Haut LEVEQUE

Pessac, France

CHU de Reims

Reims, France

IUCT Oncopole

Toulouse, France

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NCT05246345


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