Easily Applicable Predictive Score for Differential Diagnosis of Prefibrotic Primary Myelofibrosis from Essential Thrombocythemia

Author:

Lekovic Danijela12ORCID,Bogdanovic Andrija12ORCID,Sobas Marta3ORCID,Arsenovic Isidora1,Smiljanic Mihailo1,Ivanovic Jelena1,Bodrozic Jelena1ORCID,Cokic Vladan4ORCID,Milic Natasa25

Affiliation:

1. Clinic of Hematology, University Clinical Center Serbia, 11000 Belgrade, Serbia

2. Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia

3. Department of Hematology, Blood Neoplasms and Bone Marrow Transplantation, Wroclaw Medical University, 50-367 Wroclaw, Poland

4. Institute for Medical Research, University of Belgrade, 11000 Belgrade, Serbia

5. Institute of Medical Statistics & Informatics, University of Belgrade, 11000 Belgrade, Serbia

Abstract

Essential thrombocythemia (ET) and prefibrotic primary myelofibrosis (prePMF) initially have a similar phenotypic presentation with thrombocytosis. The aim of our study was to determine significant clinical-laboratory parameters at presentation to differentiate prePMF from ET as well as to develop and validate a predictive diagnostic prePMF model. This retrospective study included 464 patients divided into ET (289 pts) and prePMF (175 pts) groups. The model was built using data from a development cohort (229 pts; 143 ET, 86 prePMF), which was then tested in an internal validation cohort (235 pts; 146 ET, 89 prePMF). The most important prePMF predictors in the multivariate logistic model were age ≥ 60 years (RR = 2.2), splenomegaly (RR = 13.2), and increased lactat-dehidrogenase (RR = 2.8). Risk scores were assigned according to derived relative risk (RR) for age ≥ 60 years (1 point), splenomegaly (2 points), and increased lactat-dehidrogenase (1 point). Positive predictive value (PPV) for pre-PMF diagnosis with a score of ≥points was 69.8%, while for a score of ≥3 it was 88.2%. Diagnostic performance had similar values in the validation cohort. In MPN patients with thrombocytosis at presentation, the application of the new model enables differentiation of pre-PMF from ET, which is clinically relevant considering that these diseases have different prognoses and treatments.

Funder

The Ministry of Science, Technological Development and Innovation of The Republic of Serbia

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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