Does Outcome/Survival of Patients With Myelodysplastic Syndromes Should Be Predicted by Reduced Levels of ADAMTS-13? Results From a Pilot Study.

ADAMTS-13 (a disentegrin-like and Metalloprotease with Thrombospondin type 1 motif) Disease progression Myelodysplastic syndromes Surrogate marker Von Willebrand factor (vWF) cleaving protease

Journal

Clinical lymphoma, myeloma & leukemia
ISSN: 2152-2669
Titre abrégé: Clin Lymphoma Myeloma Leuk
Pays: United States
ID NLM: 101525386

Informations de publication

Date de publication:
08 2020
Historique:
received: 07 08 2019
revised: 13 11 2019
accepted: 17 12 2019
pubmed: 9 6 2020
medline: 21 8 2021
entrez: 9 6 2020
Statut: ppublish

Résumé

Von Willebrand factor (vWF) cleaving protease ADAMTS-13 has a key role for maintaining normal size of vWF. A deficiency or dysfunction of vWF cleaving protease is associated with ultra large vWF multimers and thrombotic microangiopathy. Patients with cancers have reduced levels of vWF cleaving protease. In this pilot study, we have evaluated whether or not deficiencies of ADAMTS-13 were present in myelodysplastic syndromes (MDS). Moreover, we assessed if a reduction in basal levels of ADAMTS-13 may play a role in the prognosis of MDS. We measured and compared the levels of vWF cleaving protease ADAMTS-13 in 100 patients with MDS and 35 healthy controls. Patients were divided into 2 groups according to the International Prognostic Scoring System: group I consisting of 44 patients with low-risk MDS and group II of 56 patients with high-risk MDS. Patients with high-risk and low-risk MDS presented significantly lower levels of ADAMTS-13 than controls (P < .001 and P = .0177, respectively). High-risk patients had significantly lower levels of ADAMTS-13 when compared with the low-risk group (P < .001). We found that reduced levels of ADAMTS-13 have a relationship with overall survival (P < .001). Statistical analysis showed that ADAMTS-13 correlates with cytogenetics (P < .001) and a tendency of slight correlation with platelet count and basal levels of ADAMTS-13 (R, 0.35; P value, 0.001). Moreover, we found that levels of ADAMTS-13 have correlation with response to treatment (P < .001). ADAMTS-13 in MDS might represent a surrogate marker of prognosis, response to therapy, or disease progression. Further studies are needed.

Identifiants

pubmed: 32507387
pii: S2152-2650(20)30001-X
doi: 10.1016/j.clml.2019.12.016
pii:
doi:

Substances chimiques

ADAMTS13 Protein EC 3.4.24.87
ADAMTS13 protein, human EC 3.4.24.87

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e461-e467

Informations de copyright

Copyright © 2020. Published by Elsevier Inc.

Auteurs

Roberto Castelli (R)

Department of Biomedical and Clinical Sciences, University of Milan, Luigi Sacco Hospital Milan, Milan, Italy. Electronic address: roberto.castelli@unimi.it.

Luigi Bergamaschini (L)

Department of Biomedical and Clinical Sciences, University of Milan, Luigi Sacco Hospital Milan, Milan, Italy.

Thomas Teatini (T)

Department of Biomedical and Clinical Sciences, University of Milan, Luigi Sacco Hospital Milan, Milan, Italy.

Luca Cilumbriello (L)

Department of Biomedical and Clinical Sciences, University of Milan, Luigi Sacco Hospital Milan, Milan, Italy.

Riccardo Schiavon (R)

Department of Biomedical and Clinical Sciences, University of Milan, Luigi Sacco Hospital Milan, Milan, Italy.

Paolo Gallipoli (P)

Department of Hematology, Cambridge Institute for Medical Research, Cambridge University, Cambridge, UK.

Giorgio Lambertenghi Deliliers (GL)

Fondazione Matarelli Milano, Milan, Italy.

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Classifications MeSH