Literature DB >> 21219298

Modulation of JAK2 V617F allele burden dynamics by hydroxycarbamide in polycythaemia vera and essential thrombocythaemia patients.

Carlos Besses1, Alberto Alvarez-Larrán, Luz Martínez-Avilés, Sergi Mojal, Raquel Longarón, Antonio Salar, Lourdes Florensa, Sergi Serrano, Beatriz Bellosillo.   

Abstract

The modulation of JAK2 V617F allele burden dynamics was prospectively analysed in 47 patients (26 polycythaemia vera [PV] and 21 essential thrombocythaemia [ET]) treated with first-line hydroxyurea (HU) and compared with the JAK2 V617F dynamics of a control group of 45 PV and ET patients. A partial molecular response (PMR), according to European Leukaemia Net criteria, was observed in 27/47 (57%) patients. Median time to PMR was 14 months (3-66) with a probability of PMR at 3 years of 57%. A significant decrease in JAK2 V617F allele load was observed at 36 months both in PV and ET patients, being the reduction in PV higher than in ET patients (P = 0·01). A haematocrit ≥0·45 L/L was associated with a higher probability of attaining a PMR (HR:3·4; 95%CI:1·02-11·6, P = 0·04). Control group showed a slight increase of JAK2 V617F allele burden over time. The reduction in the mutated allele load comparing treated patients versus controls was highly significant both in PV and ET, demonstrating a clear effect of HU on the JAK2 V617F allele burden. In conclusion, first-line HU can attain PMR in more than 50% of newly diagnosed PV and ET patients, with a continuous decrease of the JAK2 V617F allele burden in PV patients during treatment.
© 2011 Blackwell Publishing Ltd.

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Year:  2011        PMID: 21219298     DOI: 10.1111/j.1365-2141.2010.08467.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  9 in total

1.  Decrease in JAK2 V617F allele burden is not a prerequisite to clinical response in patients with polycythemia vera.

Authors:  Emil Kuriakose; Katherine Vandris; Y Lynn Wang; William Chow; Amy V Jones; Paul Christos; Nicholas C P Cross; Richard T Silver
Journal:  Haematologica       Date:  2011-11-18       Impact factor: 9.941

2.  Consequences of the JAK2V617F allele burden for the prediction of transformation into myelofibrosis from polycythemia vera and essential thrombocythemia.

Authors:  Shuichi Shirane; Marito Araki; Soji Morishita; Yoko Edahiro; Yoshitaka Sunami; Yumi Hironaka; Masaaki Noguchi; Michiaki Koike; Eriko Sato; Akimichi Ohsaka; Norio Komatsu
Journal:  Int J Hematol       Date:  2014-12-19       Impact factor: 2.490

3.  Clonal analyses reveal associations of JAK2V617F homozygosity with hematologic features, age and gender in polycythemia vera and essential thrombocythemia.

Authors:  Anna L Godfrey; Edwin Chen; Francesca Pagano; Yvonne Silber; Peter J Campbell; Anthony R Green
Journal:  Haematologica       Date:  2013-05       Impact factor: 9.941

4.  JAK2 Inhibition: Reviewing a New Therapeutical Option in Myeloproliferative Neoplasms.

Authors:  Mar Bellido; Peter A W Te Boekhorst
Journal:  Adv Hematol       Date:  2012-02-16

5.  Leukemic transformation driven by an ASXL1 mutation after a JAK2V617F-positive primary myelofibrosis: clonal evolution and hierarchy revealed by next-generation sequencing.

Authors:  Francisca Ferrer-Marín; Beatriz Bellosillo; Luz Martínez-Avilés; Gloria Soler; Pablo Carbonell; Ginés Luengo-Gil; Eva Caparrós; José M Torregrosa; Carlos Besses; Vicente Vicente
Journal:  J Hematol Oncol       Date:  2013-09-08       Impact factor: 17.388

Review 6.  Monitoring Minimal Residual Disease in the Myeloproliferative Neoplasms: Current Applications and Emerging Approaches.

Authors:  Karl Haslam; Stephen E Langabeer
Journal:  Biomed Res Int       Date:  2016-10-20       Impact factor: 3.411

7.  Assessment of the interlaboratory variability and robustness of JAK2V617F mutation assays: A study involving a consortium of 19 Italian laboratories.

Authors:  Margherita Perricone; Francesca Palandri; Emanuela Ottaviani; Mario Angelini; Laura Bagli; Enrica Bellesia; Meris Donati; Donato Gemmati; Patrizia Zucchini; Stefania Mancini; Valentina Marchica; Serena Trubini; Giovanna De Matteis; Silvia Di Zacomo; Mosè Favarato; Annamaria Fioroni; Caterina Bolzonella; Giorgia Maccari; Filippo Navaglia; Daniela Gatti; Luisa Toffolatti; Linda Orlandi; Vèronique Laloux; Marco Manfrini; Piero Galieni; Barbara Giannini; Alessia Tieghi; Sara Barulli; Maria Luisa Serino; Monica Maccaferri; Anna Rita Scortechini; Nicola Giuliani; Daniele Vallisa; Massimiliano Bonifacio; Patrizia Accorsi; Cristina Salbe; Vinicio Fazio; Milena Gusella; Eleonora Toffoletti; Marzia Salvucci; Mirija Svaldi; Filippo Gherlinzoni; Francesca Cassavia; Francesco Orsini; Giovanni Martinelli
Journal:  Oncotarget       Date:  2017-05-16

8.  Essential thrombocythemia: a rare disease in childhood.

Authors:  Julia Maimone Beatrice; Marlene Pereira Garanito
Journal:  Rev Bras Hematol Hemoter       Date:  2013

9.  JAK2V617F Allele Burden Measurement in Peripheral Blood of Iranian Patients with Myeloproliferative Neoplasms and Effect of Hydroxyurea on JAK2V617F Allele Burden.

Authors:  Shirin Ferdowsi; Seyed H Ghaffari; Naser Amirizadeh; Azita Azarkeivan; Kamran Atarodi; Mohammad Faranoush; Gholamreza Toogeh; Reza Shirkoohi; Mohammad Vaezi; Mahtab Maghsoodlu; Kamran Alimoghaddam; Ardeshir Ghavamzadeh; Hosein Teimori Naghadeh
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2016-04-01
  9 in total

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