Leukemic Involvement Is a Common Feature in Waldenström Macroglobulinemia at Diagnosis

Author:

Montesdeoca Sara12,García-Gisbert Nieves34ORCID,Calvo Xavier25ORCID,Arenillas Leonor25ORCID,Román David25ORCID,Fernández-Rodríguez Concepción34,Navarro Rosa25,Costan Beatriz25,Vela María del Carmen34,Camacho Laura34,Abella Eugènia46,Colomo Lluís27ORCID,Salido Marta28,Puiggros Anna28ORCID,Florensa Lourdes25,Espinet Blanca28,Bellosillo Beatriz34,Ferrer del Álamo Ana25

Affiliation:

1. Laboratori d’Hematologia, Servei Diagnòstic de Laboratori, Hospital Sant Joan de Déu, Esplugues de Llobregat, 08950 Barcelona, Spain

2. Grup de Recerca Translacional en Neoplasies Hematològiques (GRETNHE), Hospital del Mar Research Institute (IMIM), 08003 Barcelona, Spain

3. Laboratori de Biologia Molecular, Servei de Patologia, Hospital del Mar, 08003 Barcelona, Spain

4. Grup de Recerca Clínica Aplicada en Neoplàsies Hematològiques, Hospital del Mar Research Institute (IMIM), 08003 Barcelona, Spain

5. Laboratori de Citologia Hematològica, Servei de Patologia, Hospital del Mar, 08003 Barcelona, Spain

6. Servei d’Hematologia Clínica, Hospital del Mar, 08003 Barcelona, Spain

7. Servei de Patologia, Hospital del Mar, 08003 Barcelona, Spain

8. Laboratori de Citogenètica Molecular, Servei de Patologia, Hospital del Mar, 08003 Barcelona, Spain

Abstract

Waldenström Macroglobulinemia (WM) is a lymphoplasmacytic lymphoma with bone marrow (BM) involvement and IgM monoclonal gammopathy. To date, no studies have focused specifically on peripheral blood (PB) involvement. In this study, 100 patients diagnosed with WM according to the World Health Organization (WHO) criteria were included based on the demonstration of MYD88mut in BM and the availability of PB multiparametric flow cytometry (MFC) analysis. Leukemic involvement by MFC was detected in 50/100 patients. A low percentage of mature small lymphocytes in PB smears was observed in only 15 cases. MYD88mut by AS-qPCR was detected in PB in 65/100 cases. In cases with leukemic expression by MFC, MYD88mut was detected in all cases, and IGH was rearranged in 44/49 cases. In 21/50 patients without PB involvement by MFC, molecular data were consistent with circulating disease (MYD88mut by AS-qPCR 3/50, IGH rearranged 6/50, both 12/50). Therefore, PB involvement by standard techniques was detected in 71/100 patients. MYD88mut was detected in PB by dPCR in 9/29 triple negative cases. Overall, 80% of the patients presented PB involvement by any technique. Our findings support the role of PB MFC in the evaluation of patients with IgM monoclonal gammopathy and provide reliable information on correlation with molecular features. The development of a feasible MFC assay may stand as an objective tool in the classification of mature B cell neoplasms presenting with IgM monoclonal gammopathy.

Funder

Instituto de Salud Carlos III

Societat Catalana d’Hematologia i Hemoteràpia

Publisher

MDPI AG

Subject

Cancer Research,Oncology

Reference33 articles.

1. Swerdlow, S.H., Campo, E., Harris, N.L., Jaffe, E.S., Pileri, S.A., Stein, H., and Thiele, J. (2017). WHO Classification of Tumours of Hematopoietic and Lymphoid Tissues, IARC. [4th ed.].

2. The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms;Alaggio;Leukemia,2022

3. The International Consensus Classification of Mature Lymphoid Neoplasms: A report from the Clinical Advisory Committee;Campo;Blood,2022

4. Progression in smoldering Waldenström macroglobulinemia: Long-term results;Kyle;Blood,2012

5. Progression Risk Stratification of Asymptomatic Waldenström Macroglobulinemia;Bustoros;J. Clin. Oncol.,2019

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