Hamostaseologie
DOI: 10.1055/a-2159-8767
Original Article

Arterial and Venous Thromboembolic Complications in 832 Patients with BCR-ABL-Negative Myeloproliferative Neoplasms

Kai Wille*
1   University Clinic for Hematology, Oncology, Hemostaseology and Palliative Care, Johannes Wesling Medical Center Minden, University of Bochum, Bochum, Germany
,
Eva Deventer*
1   University Clinic for Hematology, Oncology, Hemostaseology and Palliative Care, Johannes Wesling Medical Center Minden, University of Bochum, Bochum, Germany
,
Parvis Sadjadian
1   University Clinic for Hematology, Oncology, Hemostaseology and Palliative Care, Johannes Wesling Medical Center Minden, University of Bochum, Bochum, Germany
,
Tatjana Becker
1   University Clinic for Hematology, Oncology, Hemostaseology and Palliative Care, Johannes Wesling Medical Center Minden, University of Bochum, Bochum, Germany
,
Vera Kolatzki
1   University Clinic for Hematology, Oncology, Hemostaseology and Palliative Care, Johannes Wesling Medical Center Minden, University of Bochum, Bochum, Germany
,
Karlo Hünerbein
1   University Clinic for Hematology, Oncology, Hemostaseology and Palliative Care, Johannes Wesling Medical Center Minden, University of Bochum, Bochum, Germany
,
Raphael Meixner
2   Core Facility Statistical Consulting, Helmholtz Zentrum München, Munich, Germany
,
Marina Jiménez-Muñoz
2   Core Facility Statistical Consulting, Helmholtz Zentrum München, Munich, Germany
,
Christiane Fuchs
2   Core Facility Statistical Consulting, Helmholtz Zentrum München, Munich, Germany
3   Faculty of Business Administration and Economics, Bielefeld University, Bielefeld, Germany
,
Martin Griesshammer
1   University Clinic for Hematology, Oncology, Hemostaseology and Palliative Care, Johannes Wesling Medical Center Minden, University of Bochum, Bochum, Germany
› Author Affiliations
Funding No funding was committed for this study.

Abstract

Arterial (ATE) and venous (VTE) thromboembolic complications are common causes of morbidity and mortality in BCR-ABL-negative myeloproliferative neoplasms (MPNs). However, there are few studies that include all MPN subtypes and focus on both MPN-associated ATE and VTE. In our single-center retrospective study of 832 MPN patients, a total of 180 first thromboembolic events occurred during a median follow-up of 6.6 years (range: 0–37.6 years), of which 105 were VTE and 75 were ATE. The probability of a vascular event at the end of the follow-up period was 36.2%, and the incidence rate for all first ATE/VTE was 2.43% patient/year. The most frequent VTE localizations were deep vein thrombosis with or without pulmonary embolism (incidence rate: 0.59% patient/year), while strokes were the most frequent ATE with an incidence rate of 0.32% patient/year. When comparing the group of patients with ATE/VTE (n = 180) and the group without such an event (n = 652) using multivariate Cox regression analyses, patients with polycythemia vera (hazard ratio [HR]: 1.660; [95% confidence interval [CI] 1.206, 2.286]) had a significantly higher risk of a thromboembolic event than the other MPN subtypes. In contrast, patients with a CALR mutation had a significantly lower risk of thromboembolism compared with JAK2-mutated MPN patients (HR: 0.346; [95% CI: 0.172, 0.699]). In summary, a high incidence of MPN-associated VTE and ATE was observed in our retrospective study. While PV patients or generally JAK2-mutated MPN patients had a significantly increased risk of such vascular events, this risk was reduced in CALR-mutated MPN patients.

Availability of Data and Materials

The data that support the findings of this study are available from the corresponding author upon reasonable request.


Ethical Approval

The questionnaire and study protocol for this retrospective study were approved by the Ethics Committee of the Ruhr-Universität Bochum, based in Bad Oeynhausen.


Consent to Participate

Written consent was obtained from all individual participants included in the study.


Code Availability

Not applicable.


* Both authors contributed equally to this work.




Publication History

Received: 02 May 2023

Accepted: 24 August 2023

Article published online:
09 October 2023

© 2023. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
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