Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Bone marrow mesenchymal stem cells in Waldenström Macroglobulinemia

Official title: Phenotypic and Functional Study of Bone Marrow Mesenchymal Stem Cells in Waldenström Macroglobulinemia

Run by Centre Hospitalier Universitaire, Amiens · NCT07471074 · Data updated 2026-11-12

This project will take bone marrow samples to test how mesenchymal stem cells behave in people with Waldenström Macroglobulinemia.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment50 (estimated)
SponsorCentre Hospitalier Universitaire, Amiens
Academic / other
Locations1 site (Amiens)
StatusRecruiting
StartedFebruary 10, 2026
Main results expectedMarch 2028
Study endsMarch 2028
Registry record updatedMarch 13, 2026
Trial IDNCT07471074 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with a confirmed diagnosis of Waldenström Macroglobulinemia who require treatment within three months, can give informed consent, and have social security coverage are eligible.

Probably not a fit

Patients who do not need treatment, who have other chronic lymphoid malignancies, who have transformed histology, or who cannot undergo bone marrow sampling are unlikely to benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Researchers will collect bone marrow samples from consenting patients with Waldenström Macroglobulinemia who require treatment and isolate mesenchymal stem cells for laboratory study. The cells will be characterized for their surface phenotype and functional properties and compared with expected normal features of the bone marrow niche. The work will explore how stromal cell abnormalities and microenvironment signals relate to disease features and common mutations such as MYD88 and CXCR4. Findings are intended to improve biological understanding of tumor–niche interactions rather than to test a therapeutic intervention.

Why it matters

Potential benefit: If successful, this work could clarify how the bone marrow environment supports Waldenström cells and point to biomarkers or targets for future therapies.

How similar studies have gone: Previous work has described immune-cell abnormalities in Waldenström disease and some microenvironment studies exist, but detailed functional data specifically on bone marrow mesenchymal stem cells remains limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients with WM, meeting the diagnostic criteria defined at the 2nd WM Workshop, revised at the 9th international workshop.
* Patients requiring treatment within 3 months according to the recommendations defined at the 2nd Workshop on WM.
* Patients having given their consent for this study.
* Affiliation to a social security scheme.

Exclusion Criteria:

* Patients with other chronic lymphoid hemopathies. Particular care should be taken to exclude other closely related lymphoplasmacytic proliferations, especially marginal zone lymphomas.
* Patients with WM who have undergone histological transformation to a lymphoma other than diffuse large B- cell lymphoma.
* Absence of consent for this study.
* Patients under court protection, subjects participating in another study with an exclusion period still in progress at pre-inclusion.

Where it's running

  • CHU Amiens
    Amiens, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.