Targeted deep sequencing in polycythemia vera and essential thrombocythemia

Author:

Tefferi Ayalew1,Lasho Terra L.1,Guglielmelli Paola2,Finke Christy M.1,Rotunno Giada2,Elala Yoseph1,Pacilli Annalisa2,Hanson Curtis A.3,Pancrazzi Alessandro2,Ketterling Rhett P.4,Mannarelli Carmela2,Barraco Daniela1,Fanelli Tiziana2,Pardanani Animesh1,Gangat Naseema1,Vannucchi Alessandro M.2

Affiliation:

1. Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, MN;

2. Centro Ricerca e Innovazione Malattie Mieloproliferative, Azienda Ospedaliera Universitaria Careggi, and Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy; and

3. Division of Hematopathology and

4. Division of Cytogenetics, Department of Laboratory Medicine, Mayo Clinic, Rochester, MN

Abstract

Key Points More than half of patients with PV or ET harbor DNA mutations/variants other than JAK2/CALR/MPL. The presence of some of these mutations adversely affects overall, leukemia-free, or myelofibrosis-free survival.

Publisher

American Society of Hematology

Subject

Hematology

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