Literature DB >> 19278953

Response criteria for essential thrombocythemia and polycythemia vera: result of a European LeukemiaNet consensus conference.

Giovanni Barosi1, Gunnar Birgegard, Guido Finazzi, Martin Griesshammer, Claire Harrison, Hans Carl Hasselbalch, Jean-Jacques Kiladjian, Eva Lengfelder, Mary Frances McMullin, Francesco Passamonti, John T Reilly, Alessandro M Vannucchi, Tiziano Barbui.   

Abstract

European experts were convened to develop a definition of response to treatment in polycythemia vera (PV) and essential thrombocythemia (ET). Clinicohematologic (CH), molecular, and histologic response categories were selected. In ET, CH complete response (CR) was: platelet count less than or equal to 400 x 10(9)/L, no disease-related symptoms, normal spleen size, and white blood cell count less than or equal to 10 x 10(9)/L. Platelet count less than or equal to 600 x 10(9)/L or a decrease greater than 50% was partial response (PR). In PV, CH-CR was: hematocrit less than 45% without phlebotomy, platelet count less than or equal to 400 x 10(9)/L, white blood cell count less than or equal to 10 x 10(9)/L, and no disease-related symptoms. A hematocrit less than 45% without phlebotomy or response in 3 or more of the other criteria was defined as PR. In both ET and in PV, molecular CR was a reduction of any molecular abnormality to undetectable levels. Molecular PR was defined as a reduction more than or equal to 50% in patients with less than 50% mutant allele burden, or a reduction more than or equal to 25% in patients with more than 50% mutant allele burden. Bone marrow histologic response in ET was judged on megakaryocyte hyperplasia while on cellularity and reticulin fibrosis in PV. The combined use of these response definitions should help standardize the design and reporting of clinical studies.

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Year:  2009        PMID: 19278953     DOI: 10.1182/blood-2008-09-176818

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  84 in total

1.  Experience with pegylated interferon α-2a in advanced myeloproliferative neoplasms in an international cohort of 118 patients.

Authors:  Krisstina Gowin; Prakash Thapaliya; Jan Samuelson; Claire Harrison; Deepti Radia; Bjorn Andreasson; John Mascarenhas; Alessandro Rambaldi; Tiziano Barbui; Catherine J Rea; John Camoriano; Amy Gentry; Jean-Jacques Kiladjian; Casey O'Connell; Ruben Mesa
Journal:  Haematologica       Date:  2012-03-14       Impact factor: 9.941

2.  Hydroxyurea does not appreciably reduce JAK2 V617F allele burden in patients with polycythemia vera or essential thrombocythemia.

Authors:  Elisabetta Antonioli; Alessandra Carobbio; Lisa Pieri; Alessandro Pancrazzi; Paola Guglielmelli; Federica Delaini; Vanessa Ponziani; Niccolò Bartalucci; Lorenzo Tozzi; Alberto Bosi; Alessandro Rambaldi; Tiziano Barbui; Alessandro M Vannucchi
Journal:  Haematologica       Date:  2010-04-23       Impact factor: 9.941

3.  Characteristics and treatment of polycythemia vera patients in clinical practice: a multicenter chart review on 1476 individuals in Germany.

Authors:  Kathleen Jentsch-Ullrich; Judith Eberhardt; Vanja Zeremski; Michael Koehler; Denise Wolleschak; Florian H Heidel
Journal:  J Cancer Res Clin Oncol       Date:  2016-07-18       Impact factor: 4.553

Review 4.  Janus kinase inhibitors for the treatment of myeloproliferative neoplasias and beyond.

Authors:  Alfonso Quintás-Cardama; Hagop Kantarjian; Jorge Cortes; Srdan Verstovsek
Journal:  Nat Rev Drug Discov       Date:  2011-02       Impact factor: 84.694

Review 5.  JAK2 inhibitors: what's the true therapeutic potential?

Authors:  Fabio P S Santos; Srdan Verstovsek
Journal:  Blood Rev       Date:  2010-11-20       Impact factor: 8.250

6.  Perspectives on thrombosis in essential thrombocythemia and polycythemia vera: is leukocytosis a causative factor?

Authors:  Tiziano Barbui; Alessandra Carobbio; Alessandro Rambaldi; Guido Finazzi
Journal:  Blood       Date:  2009-04-16       Impact factor: 22.113

7.  Effect of busulfan on JAK2V617F allele burden.

Authors:  Maria Luigia Randi; Claudia Santarossa; Edoardo Peroni; Elisabetta Cosi; Elena Duner; Irene Bertozzi; Fabrizio Fabris
Journal:  Haematologica       Date:  2014-01-03       Impact factor: 9.941

8.  Use of the 46/1 haplotype to model JAK2(V617F) clonal architecture in PV patients: clonal evolution and impact of IFNα treatment.

Authors:  S Hasan; B Cassinat; N Droin; J P Le Couedic; F Favale; B Monte-Mor; C Lacout; M Fontenay; C Dosquet; C Chomienne; E Solary; J L Villeval; N Casadevall; J J Kiladjian; W Vainchenker; I Plo
Journal:  Leukemia       Date:  2013-10-22       Impact factor: 11.528

9.  JAK2V617F allele burden is reduced by busulfan therapy: a new observation using an old drug.

Authors:  Emil T Kuriakose; Stefani Gjoni; Y Lynn Wang; Ruth Baumann; Amy V Jones; Nicholas C P Cross; Richard T Silver
Journal:  Haematologica       Date:  2013-11       Impact factor: 9.941

Review 10.  Therapeutic options for patients with polycythemia vera and essential thrombocythemia refractory/resistant to hydroxyurea.

Authors:  Matjaz Sever; Kate J Newberry; Srdan Verstovsek
Journal:  Leuk Lymphoma       Date:  2014-03-17
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