Mast cell density and its clinical relevance in Waldenström's macroglobulinemia.

Waldenström's macroglobulinemia mast cells tumor biology

Journal

EJHaem
ISSN: 2688-6146
Titre abrégé: EJHaem
Pays: United States
ID NLM: 101761942

Informations de publication

Date de publication:
May 2022
Historique:
received: 15 12 2021
revised: 27 12 2021
accepted: 29 12 2021
entrez: 18 7 2022
pubmed: 19 7 2022
medline: 19 7 2022
Statut: epublish

Résumé

The presence of numerous mast cells (MCs) mixed with tumor cells in the bone marrow (BM) is a hallmark of the diagnosis of Waldenström's macroglobulinemia (WM). MCs have been shown to support lymphoplasmacytic cell growth, but there is thus far no demonstration of the prognostic impact of BM MC density in WM. We investigated BM MC density by sensitive and specific digital quantification, allowing the analysis of a large area infiltrated by BM tumor cells. A total of 65 WM patients were investigated, including 54 at diagnosis and 11 at relapse. Tryptase and CD20 immunohistochemisty staining was performed on contiguous sections of deparaffinized BM trephine biopsies. After numerization of each section, the BM surface area was manually marked out, excluding the bone framework and adipocytes to limit the analyses to only hematopoietic tissue. MCs were assessed using a digital tool previously used to quantify immune-cell infiltrates on tumor-tissue sections. Deep next-generation sequencing and allele-specific PCR were used to explore the

Identifiants

pubmed: 35846063
doi: 10.1002/jha2.378
pii: JHA2378
pmc: PMC9176068
doi:

Types de publication

Journal Article

Langues

eng

Pagination

371-378

Informations de copyright

© 2022 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd.

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to declare.

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Auteurs

Richard Lemal (R)

Laboratoire d'Histocompatibilité, Centre de Biologie, CHU de Clermont-Ferrand Université Clermont Auvergne Clermont Ferrand France.
Hématologie Clinique et Thérapie Cellulaire CHU Clermont-Ferrand EA7453 CHELTER CIC1405 Université Clermont Auvergne Clermont Ferrand France.

Stéphanie Poulain (S)

"CANcer Heterogeneity Plasticity and Resistance to THERapies" INSERM 1277-CNRS 9020 UMRS 12 University of Lille Lille France.
Service d'Hématologie Cellulaire Centre de Biologie Pathologie Lille France.

Albane Ledoux-Pilon (A)

Anatomie Pathologique CHU Clermont-Ferrand Université Clermont Auvergne Clermont Ferrand France.

Lauren Veronese (L)

Service de Cytogénétique Médicale CHU Clermont-Ferrand INSERM U1240 IMOST Université Clermont Auvergne Clermont Ferrand France.

Andrei Tchirkov (A)

Service de Cytogénétique Médicale CHU Clermont-Ferrand INSERM U1240 IMOST Université Clermont Auvergne Clermont Ferrand France.

Benjamin Lebecque (B)

Hématologie Clinique et Thérapie Cellulaire CHU Clermont-Ferrand EA7453 CHELTER CIC1405 Université Clermont Auvergne Clermont Ferrand France.
Service d'Hématologie Biologique CHU Clermont-Ferrand Université Clermont Auvergne Clermont Ferrand France.

Thomas Tassin (T)

Hématologie Clinique et Thérapie Cellulaire CHU Clermont-Ferrand EA7453 CHELTER CIC1405 Université Clermont Auvergne Clermont Ferrand France.
Service d'Hématologie Biologique CHU Clermont-Ferrand Université Clermont Auvergne Clermont Ferrand France.

Jacques-Olivier Bay (JO)

Hématologie Clinique et Thérapie Cellulaire CHU Clermont-Ferrand EA7453 CHELTER CIC1405 Université Clermont Auvergne Clermont Ferrand France.

Frédéric Charlotte (F)

Anatomie Pathologique APHP La Pitié Salpêtrière Paris France.

Florence Nguyen-Khac (F)

Service d'Hématologie Biologique Sorbonne Université Hôpital Pitié-Salpêtrière Centre de Recherche des Cordeliers Paris France.

Marc Berger (M)

Service d'Hématologie Biologique CHU Clermont-Ferrand Université Clermont Auvergne Clermont Ferrand France.

Catherine Godfraind (C)

Anatomie Pathologique CHU Clermont-Ferrand Université Clermont Auvergne Clermont Ferrand France.

Loïc Ysebaert (L)

IUCT Oncopole Hématologie Clinique Toulouse France.

Frédéric Davi (F)

La Pitié Salpêtrière APHP Laboratoire d'Hématologie Paris France.

Bruno Pereira (B)

Direction de la recherche clinique Unité Biostatistique Clermont Ferrand France.

Véronique Leblond (V)

Hématologie Clinique APHP UPMC La Pitié Salpêtrière Paris France.

Olivier Hermine (O)

Hématologie Clinique APHP, IMAGINE Institute Necker-Enfants Malades Paris France.

Romain Guièze (R)

Hématologie Clinique et Thérapie Cellulaire CHU Clermont-Ferrand EA7453 CHELTER CIC1405 Université Clermont Auvergne Clermont Ferrand France.

Franck Pagès (F)

Immunomonitoring Plateform APHP Hôpital Européen Georges Pompidou Paris France.

Olivier Tournilhac (O)

Hématologie Clinique et Thérapie Cellulaire CHU Clermont-Ferrand EA7453 CHELTER CIC1405 Université Clermont Auvergne Clermont Ferrand France.

Classifications MeSH