Expression of Ku70/XRCC6 in Waldenström's Macroglobulinemia

NCT ID: NCT02640287

Last Updated: 2021-08-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

55 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-02-29

Study Completion Date

2020-07-01

Brief Summary

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Waldenström's macroglobulinemia is a rare disease whose pathophysiology remains at present poorly understood, although a recurrent mutation (L265P MYD88) has recently been described. Unlike other lymphoproliferative disorders, there is a defect in isotype switching, mechanism involving AID and NHEJ complex. Using a two-dimensional electrophoresis technology, our group showed that MW had a specific proteomic profile, and one of the differentially expressed proteins is Ku70 (encoded by XRCC6 belonging to NHEJ complex) .

The investigators purpose to explore the mechanisms of underexpression of Ku70/XRCC6 (genetic or epigenetic modification) in comparison with other lymphoid malignancies and normal B cells.

Detailed Description

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Conditions

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Waldenström Macroglobulinemia

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Waldenström macroglobulinemia

Patients with diagnosis of Waldenström macroglobulinemia

Group Type EXPERIMENTAL

Blood or bone marrow samples

Intervention Type BIOLOGICAL

Others B-cell malignancies

Patients with diagnosis of Chronic Lymphocytic Leukemia, Splenic Marginal Zone Lymphoma or Multiple Myeloma

Group Type EXPERIMENTAL

Blood or bone marrow samples

Intervention Type BIOLOGICAL

Healthy subjects

Control healthy subjects without B-cell malignancy

Group Type OTHER

Blood or bone marrow samples

Intervention Type BIOLOGICAL

Interventions

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Blood or bone marrow samples

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

* Patient over 18 years, affiliated to the social regimen
* Written consent collected

MW group :

* Patient with a diagnosis of MW according to WHO criteria (based on the results of serum protein electrophoresis, bone marrow analysis with immunophenotyping, cytogenetic analysis and mutation L265P MyD88)

Other SLP :

* Patient with diagnosis of Chronic Lymphocytic Leukemia, Splenic Marginal Zone Lymphoma or Multiple Myeloma

Healthy volunteers :

* volunteers without blood disorders

Exclusion Criteria

* Women of childbearing age who do not have an effective means of contraception
* Pregnant or nursing
* Demonstration of a kappa or lambda monotype on B lymphocytes
* healthy volunteer with B-cell malignancy
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Central Hospital, Nancy, France

OTHER

Sponsor Role lead

Responsible Party

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Aurore PERROT

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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CHRU Nancy

Vandœuvre-lès-Nancy, , France

Site Status

Countries

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France

Other Identifiers

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2015-A01516-43

Identifier Type: -

Identifier Source: org_study_id

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