The management and outcomes of patients with myelodysplastic syndrome with persistent severe thrombocytopenia: An observational single centre registry study.


Journal

Leukemia research
ISSN: 1873-5835
Titre abrégé: Leuk Res
Pays: England
ID NLM: 7706787

Informations de publication

Date de publication:
01 2019
Historique:
received: 05 09 2018
revised: 07 12 2018
accepted: 10 12 2018
pubmed: 24 12 2018
medline: 17 7 2019
entrez: 24 12 2018
Statut: ppublish

Résumé

Severe thrombocytopenia affects 10% of patients with myelodysplastic syndrome (MDS) and is associated with poor outcomes. The role for prophylactic platelet transfusions in the outpatient setting is unknown. To audit treatments, bleeding rates, and transfusion requirements of patients with MDS and persistent severe thrombocytopenia (PST) registered in a prospective MDS registry at our center. 99 (17%) of 586 total registry patients had PST; 28 were treated with tranexamic acid alone (TXA), 39 with TXA and prophylactic platelet transfusions (PROPH), 19 with PROPH alone, and 13 were untreated. Median duration of PST was 27 weeks and median overall survival was 0.9 years (95% CI 0.7-1.2). During the PST, 6% (6/99) of patients had a grade 4 bleeding event, from which 4 died. Platelet count at the time of grade 4 bleeding ranged from 2 to 19 × 10 Patients with MDS and PST had low rates of major bleeding but poor overall survival. Disparities in clinical practice likely relate to patient and provider heterogeneity and the lack of published evidence. The benefit of TXA and/or prophylactic platelet transfusions would be best evaluated by a randomized controlled trial.

Sections du résumé

BACKGROUND
Severe thrombocytopenia affects 10% of patients with myelodysplastic syndrome (MDS) and is associated with poor outcomes. The role for prophylactic platelet transfusions in the outpatient setting is unknown.
OBJECTIVE/METHODS
To audit treatments, bleeding rates, and transfusion requirements of patients with MDS and persistent severe thrombocytopenia (PST) registered in a prospective MDS registry at our center.
RESULTS
99 (17%) of 586 total registry patients had PST; 28 were treated with tranexamic acid alone (TXA), 39 with TXA and prophylactic platelet transfusions (PROPH), 19 with PROPH alone, and 13 were untreated. Median duration of PST was 27 weeks and median overall survival was 0.9 years (95% CI 0.7-1.2). During the PST, 6% (6/99) of patients had a grade 4 bleeding event, from which 4 died. Platelet count at the time of grade 4 bleeding ranged from 2 to 19 × 10
CONCLUSIONS
Patients with MDS and PST had low rates of major bleeding but poor overall survival. Disparities in clinical practice likely relate to patient and provider heterogeneity and the lack of published evidence. The benefit of TXA and/or prophylactic platelet transfusions would be best evaluated by a randomized controlled trial.

Identifiants

pubmed: 30580105
pii: S0145-2126(18)30489-2
doi: 10.1016/j.leukres.2018.12.002
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

76-81

Informations de copyright

Copyright © 2018 Elsevier Ltd. All rights reserved.

Auteurs

Abi Vijenthira (A)

Postgraduate Medical Education, University of Toronto, Toronto, ON, Canada.

Devyani Premkumar (D)

Sunnybrook Health Sciences Centre, Toronto, ON, Canada.

Jeannie Callum (J)

Department of Laboratory Medicine and Molecular Diagnostics, Sunnybrook Health Sciences Centre, Canada; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto ON, Canada.

Yulia Lin (Y)

Department of Laboratory Medicine and Molecular Diagnostics, Sunnybrook Health Sciences Centre, Canada; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto ON, Canada.

Richard A Wells (RA)

Department of Hematology/Oncology, Odette Cancer Center, Sunnybrook Health Sciences Centre, Canada; Department of Medicine, University of Toronto, Toronto, ON, Canada.

Lisa Chodirker (L)

Department of Hematology/Oncology, Odette Cancer Center, Sunnybrook Health Sciences Centre, Canada; Department of Medicine, University of Toronto, Toronto, ON, Canada.

Martha Lenis (M)

Department of Hematology/Oncology, Odette Cancer Center, Sunnybrook Health Sciences Centre, Canada.

Alexandre Mamedov (A)

Department of Hematology/Oncology, Odette Cancer Center, Sunnybrook Health Sciences Centre, Canada.

Rena Buckstein (R)

Department of Hematology/Oncology, Odette Cancer Center, Sunnybrook Health Sciences Centre, Canada; Department of Medicine, University of Toronto, Toronto, ON, Canada. Electronic address: rena.buckstein@sunnybrook.ca.

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