Survival and Disease Progression in Essential Thrombocythemia Are Significantly Influenced by Accurate Morphologic Diagnosis: An International Study

Author:

Barbui Tiziano1,Thiele Juergen1,Passamonti Francesco1,Rumi Elisa1,Boveri Emanuela1,Ruggeri Marco1,Rodeghiero Francesco1,d'Amore Emanuele S.G.1,Randi Maria Luigia1,Bertozzi Irene1,Marino Filippo1,Vannucchi Alessandro M.1,Antonioli Elisabetta1,Carrai Valentina1,Gisslinger Heinz1,Buxhofer-Ausch Veronika1,Müllauer Leonhard1,Carobbio Alessandra1,Gianatti Andrea1,Gangat Naseema1,Hanson Curtis A.1,Tefferi Ayalew1

Affiliation:

1. From the Ospedali Riuniti di Bergamo, Bergamo; University of Pavia, Istituto Di Ricovero e Cura a Carattere Scientifico Policlinico San Matteo, Pavia; S. Bortolo Hospital, Vicenza; University of Padua, Padua; University of Florence, Florence, Italy; University of Cologne, Cologne, Germany; Medical University of Vienna, Vienna, Austria; and Mayo Clinic, Rochester, MN.

Abstract

PurposeThe WHO diagnostic criteria underscore the role of bone marrow (BM) morphology in distinguishing essential thrombocythemia (ET) from early/prefibrotic primary myelofibrosis (PMF). This study examined the clinical relevance of such a distinction.MethodsRepresentatives from seven international centers of excellence for myeloproliferative neoplasms convened to create a clinicopathologic database of patients previously diagnosed as having ET (N = 1,104). Study eligibility criteria included availability of treatment-naive BM specimens obtained within 1 year of diagnosis. All bone marrows subsequently underwent a central re-review.ResultsDiagnosis was confirmed as ET in 891 patients (81%) and was revised to early/prefibrotic PMF in 180 (16%); 33 patients were not evaluable. In early/prefibrotic PMF compared with ET, the 10-year survival rates (76% and 89%, respectively) and 15-year survival rates (59% and 80%, respectively), leukemic transformation rates at 10 years (5.8% and 0.7%, respectively) and 15 years (11.7% and 2.1%, respectively), and rates of progression to overt myelofibrosis at 10 years (12.3% and 0.8%, respectively) and 15 years (16.9% and 9.3%) were significantly worse. The respective death, leukemia, and overt myelofibrosis incidence rates per 100 patient-years for early/prefibrotic PMF compared with ET were 2.7% and 1.3% (relative risk [RR], 2.1; P < .001), 0.6% and 0.1% (RR, 5.2; P = .001), and 1% and 0.5% (RR, 2.0; P = .04). Multivariable analysis confirmed these findings and also identified age older than 60 years (hazard ratio [HR], 6.7), leukocyte count greater than 11 × 109/L (HR, 2.01), anemia (HR, 2.95), and thrombosis history (HR, 2.81) as additional risk factors for survival. Thrombosis and JAK2V617F incidence rates were similar between the two groups. Survival in ET was similar to the sex- and age-standardized European population.ConclusionThis study validates the clinical relevance of strict adherence to WHO criteria in the diagnosis of ET and provides important information on survival, disease complication rates, and prognostic factors in strictly WHO-defined ET and early/prefibrotic PMF.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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