Beneficial outcomes and epidemiologics of atypical electrophoretic profiles arising after allogeneic hematopoietic stem cell transplantation for myeloid malignancies.


Journal

Current research in translational medicine
ISSN: 2452-3186
Titre abrégé: Curr Res Transl Med
Pays: France
ID NLM: 101681234

Informations de publication

Date de publication:
01 2022
Historique:
received: 14 12 2020
revised: 05 11 2021
accepted: 09 11 2021
pubmed: 22 11 2021
medline: 27 1 2022
entrez: 21 11 2021
Statut: ppublish

Résumé

Atypical serum protein electrophoresis (SPE) profiles may arise in patients who received allogeneic hematopoietic stem cell transplantation (allo-HSCT), but little is known about their clinical significance. Atypical SPE combine either monoclonal and oligoclonal components, suspected on SPE and confirmed by immunofixation. The aim of the study is to analyze the incidence, the etiology and the clinical significance of atypical SPE profiles in patients who received allo-HSCT. This retrospective study enrolled 117 patients with myeloid malignancies who received an allo-HSCT between 2012 and 2018. We excluded patients with lymphoid malignancies or multiple myeloma, patients presenting atypical electrophoresis prior to transplantation and patients who died within 100 days post-transplant. Atypical SPE occurred in 42.7% of patients. The cumulative incidence of atypical profiles was significantly higher in patients with acute Graft Versus Host Disease (GVHD, p = 0.019) and in patients with Cytomegalovirus (CMV) reactivation (p = 0.0017). We observed for the first time that atypical SPE profiles mostly occurred in patients transplanted from a CMV+ donor (p = 0.031). CMV reactivation preceded the occurrence of atypical SPE in the majority of patients. We show that atypical SPE delay the relapse of the underlying malignant disease (486 vs 189 days, p = 0.006), and significantly improve overall survival (OS; 33.1 months vs 28.3 months, p = 0.049). In both univariate and multivariate analyzes, the presence of an atypical SPE is the only factor that significantly improves OS. The occurrence of atypical SPE profiles after allo-HSCT may reflect an adapted post-transplant immune response leading to favourable outcomes.

Identifiants

pubmed: 34801813
pii: S2452-3186(21)00048-9
doi: 10.1016/j.retram.2021.103322
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

103322

Informations de copyright

Copyright © 2021 Elsevier Masson SAS. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest None.

Auteurs

Kaies Hedhli (K)

Laboratoire de Biochimie, CBH, CHU Amiens-Picardie, Avenue Laennec, Amiens 80054, France.

Valentin Clichet (V)

Laboratoire d'Hématologie, CHU Amiens-Picardie, Amiens, France.

Amandine Charbonnier (A)

CHU Amiens-Picardie, Service d'Hématologie Clinique et de Thérapie Cellulaire, Amiens, France.

Sandrine Castelain (S)

Laboratoire de Virologie, CHU Amiens-Picardie, Amiens, France.

Antoine Galmiche (A)

Laboratoire de Biochimie, CBH, CHU Amiens-Picardie, Avenue Laennec, Amiens 80054, France; Equipe CHIMERE, EA 7516, Université de Picardie Jules Verne, Amiens, France.

Jean-Pierre Marolleau (JP)

CHU Amiens-Picardie, Service d'Hématologie Clinique et de Thérapie Cellulaire, Amiens, France.

Thomas Boyer (T)

Laboratoire d'Hématologie, CHU Amiens-Picardie, Amiens, France; Equipe HEMATIM, EA 4666, Université de Picardie Jules Verne, France.

Alexis Caulier (A)

CHU Amiens-Picardie, Service d'Hématologie Clinique et de Thérapie Cellulaire, Amiens, France; Equipe HEMATIM, EA 4666, Université de Picardie Jules Verne, France.

Chloé Sauzay (C)

Laboratoire de Biochimie, CBH, CHU Amiens-Picardie, Avenue Laennec, Amiens 80054, France; Equipe CHIMERE, EA 7516, Université de Picardie Jules Verne, Amiens, France. Electronic address: sauzay.chloe@chu-amiens.fr.

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Classifications MeSH