3023 Mayo Clinic Patients With Myeloproliferative Neoplasms: Risk-Stratified Comparison of Survival and Outcomes Data Among Disease Subgroups.


Journal

Mayo Clinic proceedings
ISSN: 1942-5546
Titre abrégé: Mayo Clin Proc
Pays: England
ID NLM: 0405543

Informations de publication

Date de publication:
04 2019
Historique:
received: 29 06 2018
revised: 16 07 2018
accepted: 06 08 2018
pubmed: 3 3 2019
medline: 16 10 2019
entrez: 3 3 2019
Statut: ppublish

Résumé

To document the Mayo Clinic decades-long experience with myeloproliferative neoplasms (MPNs) and provide mature risk-stratified survival data and disease complication estimates. All Mayo Clinic patients with World Health Organization-defined MPNs constituted the core study group and included those with polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (PMF). A total of 3023 consecutive patients (median age, 62 years; range, 18-96 years) were considered: 665 PV, 1076 ET, and 1282 PMF. From October 27, 1967, through December 29, 2017, 1631 deaths (54%), 183 leukemic transformations (6%), 244 fibrotic progressions (14%), and 516 thrombotic events (17%) were recorded. Median overall survival (OS) was 18 years for ET, 15 years for PV, and 4.4 years for PMF (P<.05 for all intergroup comparisons). Inferior survival was documented in patients with ET diagnosed more recently (post-1990) (P<.001), whereas survival data were time independent in PV and PMF. After conventional risk stratification, OS in low-risk ET and low-risk PV were superimposed (P=.89) but each differed significantly from that of age- and sex-matched controls (P<.001). Leukemia-free survival was similar for ET and PV (P=.22) and significantly worse with PMF (P<.001). Compared with ET, PV was associated with higher risk of fibrotic progression (P<.001). Thrombosis risk after diagnosis was highest in PV and lowest in PMF (P=.002 for PV vs ET; P=.56 for ET vs PMF; and P=.001 for PV vs PMF). This study provides the most mature survival and outcomes data in MPNs and highlights MPN subgroup risk categorization as key in appraising disease natural history. The OS was only marginally better in ET compared with PV, and PV displayed a higher risk of thrombosis and fibrotic progression.

Identifiants

pubmed: 30824279
pii: S0025-6196(18)30653-0
doi: 10.1016/j.mayocp.2018.08.022
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

599-610

Informations de copyright

Copyright © 2018 Mayo Foundation for Medical Education and Research. Published by Elsevier Inc. All rights reserved.

Auteurs

Natasha Szuber (N)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Mythri Mudireddy (M)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Maura Nicolosi (M)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Domenico Penna (D)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Rangit R Vallapureddy (RR)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Terra L Lasho (TL)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Christy Finke (C)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Kebede H Begna (KH)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Michelle A Elliott (MA)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

C Christopher Hook (CC)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Alexandra P Wolanskyj (AP)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Mrinal M Patnaik (MM)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Curtis A Hanson (CA)

Division of Hematopathology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Rhett P Ketterling (RP)

Division of Laboratory Genetics and Genomics, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Shireen Sirhan (S)

Division of Hematology, Jewish General Hospital, Montréal, Québec, Canada; Chronic Myeloid Leukemia and Myeloproliferative Neoplasms Quebec Research Group.

Animesh Pardanani (A)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Naseema Gangat (N)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN.

Lambert Busque (L)

Chronic Myeloid Leukemia and Myeloproliferative Neoplasms Quebec Research Group; Department of Laboratory Hematology, Hôpital Maisonneuve-Rosemont, Université de Montréal, Montréal, Québec, Canada.

Ayalew Tefferi (A)

Division of Hematology, Department of Internal and Laboratory Medicine, Mayo Clinic, Rochester, MN. Electronic address: tefferi.ayalew@mayo.edu.

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