Volume 85, Issue 1 pp. 14-17
Research Article
Free Access

Transfusion-dependency at presentation and its acquisition in the first year of diagnosis are both equally detrimental for survival in primary myelofibrosis—prognostic relevance is independent of IPSS or karyotype

Ayalew Tefferi

Corresponding Author

Ayalew Tefferi

Division of Hematology, Mayo Clinic, Rochester, Minnesota

Mayo Clinic, 200 First Street SW, Rochester, MN 55905Search for more papers by this author
Sergio Siragusa

Sergio Siragusa

Cattedra ed U.O. di Ematologia, Policlinico Universitario di Palermo, Palermo, Italy

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Kebede Hussein

Kebede Hussein

Division of Hematology, Mayo Clinic, Rochester, Minnesota

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Susan M. Schwager

Susan M. Schwager

Division of Hematology, Mayo Clinic, Rochester, Minnesota

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Curtis A. Hanson

Curtis A. Hanson

Division of Hematopathology, Mayo Clinic, Rochester, Minnesota

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Animesh Pardanani

Animesh Pardanani

Division of Hematology, Mayo Clinic, Rochester, Minnesota

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Francisco Cervantes

Francisco Cervantes

Hematology Department, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain

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Francesco Passamonti

Francesco Passamonti

Hematology Division, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico S Matteo, University of Pavia, Pavia, Italy

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First published: 23 October 2009
Citations: 46

Conflict of interest: Nothing to report.

Abstract

The International Prognostic Scoring System (IPSS) and karyotype are useful tools for risk stratification in primary myelofibrosis (PMF). We examined the additional prognostic impact of red blood cell transfusion need among 254 consecutive patients (median age, 59 years). Sixty-two patients (∼24%) required transfusions at diagnosis whereas 22 (∼9%) became transfusion-dependent and 170 remained transfusion-independent during the first year postdiagnosis; after a median follow-up of 55 months, the respective median survivals were 35, 25, and 117 months (P < 0.01). Multivariable analysis confirmed the IPSS- and karyotype-independent prognostic weight of transfusion status. Among IPSS intermediate-1 risk patients, overall median survival of 82 months was modified to 60 or 118 months, based on presence or absence of transfusion need, respectively (P < 0.01). The corresponding figures for intermediate-2/high risk patients were 30 and 64 months (P < 0.01). Documented causes of death did not include iron overload. We conclude that transfusion status in PMF downgrades or upgrades prognosis within specific IPSS categories; transfusion need is a marker of aggressive disease biology in PMF, as it is in myelodysplastic syndromes. Am. J. Hematol., 2010. © 2009 Wiley-Liss, Inc.

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