Literature DB >> 22627739

The European Consensus on grading of bone marrow fibrosis allows a better prognostication of patients with primary myelofibrosis.

Umberto Gianelli1, Claudia Vener, Anna Bossi, Ivan Cortinovis, Alessandra Iurlo, Nicola S Fracchiolla, Federica Savi, Alessia Moro, Federica Grifoni, Chiara De Philippis, Tommaso Radice, Silvano Bosari, Giorgio Lambertenghi Deliliers, Agostino Cortelezzi.   

Abstract

We investigated the relationship between the International Prognostic Scoring System of the International Working Group for Myelofibrosis Research and Treatment and the European Consensus on grading of bone marrow fibrosis (MF) in patients with primary myelofibrosis. We compared them in 196 consecutive primary myelofibrosis patients (median follow-up 45.7 months; range 7.4-159). International Prognostic Scoring System classified 42 cases as low risk, 73 as intermediate risk-1, 69 as intermediate risk-2, and 12 as high risk; European Consensus on grading of bone marrow fibrosis classified 83 cases as MF-0, 58 as MF-1, 41 as MF-2, and 14 as MF-3. By the time of the analysis, 30 patients (15.3%) had died. Overall median survival was 3.8 years (95% confidence interval: 3.3-4.3). Multivariate analysis confirmed that both scoring systems independently predicted survival, with hazard ratios similar to those provided by univariate analysis (respectively, 2.40 (95% confidence interval: 1.47-3.91) and 2.58 (95% confidence interval: 1.72-3.89) but the likelihood ratio increased from 19.6 of the International Prognostic Scoring System or 29.0 of the European Consensus on grading of bone MF to 42.3 when both measures were considered together. Analysis of the overall survival curves documented that patients classified as having the most favourable rate with both prognostic scores (ie low risk and MF-0) survive longer than those with only one favourable score (ie low risk but MF >0 or MF-0, but International Prognostic Scoring System >low risk). In contrast, those patients classified as having the most unfavourable rate for both scores (high risk and MF-3) have a shorter survival than those with only one unfavourable score (ie high risk but MF<3 or MF-3, but International Prognostic Scoring System <high risk). In conclusion, our analysis suggests that better prognostication can be achieved in primary myelofibrosis patients when both systems are used together.

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Year:  2012        PMID: 22627739     DOI: 10.1038/modpathol.2012.87

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  30 in total

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Authors:  Hans Michael Kvasnicka
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2.  Predictive models for splenic response to JAK-inhibitor therapy in patients with myelofibrosis.

Authors:  Kamal Menghrajani; Philip S Boonstra; Jessica A Mercer; Cecelia Perkins; Krisstina L Gowin; Alissa A Weber; Ruben Mesa; Jason R Gotlib; Lixia Wang; Jack W Singer; Moshe Talpaz
Journal:  Leuk Lymphoma       Date:  2018-09-20

3.  The clinical importance of moderate/severe bone marrow fibrosis in patients with therapy-related myelodysplastic syndromes.

Authors:  Bin Fu; Chi Young Ok; Maitrayee Goswami; Wei Xei; Jesse M Jaso; Tariq Muzzafar; Carlos Bueso-Ramos; Srdan Verstovsek; Guillermo Garcia-Manero; L Jeffrey Medeiros; Sa A Wang
Journal:  Ann Hematol       Date:  2013-05-10       Impact factor: 3.673

4.  Contribution of comorbidities and grade of bone marrow fibrosis to the prognosis of survival in patients with primary myelofibrosis.

Authors:  Danijela Lekovic; Mirjana Gotic; Maja Perunicic-Jovanovic; Ana Vidovic; Andrija Bogdanovic; Gradimir Jankovic; Vladan Cokic; Natasa Milic
Journal:  Med Oncol       Date:  2014-02-06       Impact factor: 3.064

5.  The importance of central pathology review in international trials: a comparison of local versus central bone marrow reticulin grading.

Authors:  O Pozdnyakova; S Rodig; S Bhandarkar; K Wu; J Thiele; R Hasserjian
Journal:  Leukemia       Date:  2014-09-03       Impact factor: 11.528

6.  Essential thrombocythemia with high hemoglobin levels according to the revised WHO classification.

Authors:  T Barbui; J Thiele; H M Kvasnicka; A Carobbio; A M Vannucchi; A Tefferi
Journal:  Leukemia       Date:  2014-06-03       Impact factor: 11.528

7.  Significance of thrombocytopenia in patients with primary and postessential thrombocythemia/polycythemia vera myelofibrosis.

Authors:  Lucia Masarova; Ahmad Alhuraiji; Prithviraj Bose; Naval Daver; Naveen Pemmaraju; Jorge Cortes; Sherry Pierce; Hagop Kantarjian; Srdan Verstovsek
Journal:  Eur J Haematol       Date:  2018-01-17       Impact factor: 2.997

8.  Primary autoimmune myelofibrosis with severe thrombocytopenia mimicking immune thrombocytopenia: A case report.

Authors:  Jian Hua; Shu Matayoshi; Tomoyuki Uchida; Morihiro Inoue; Masao Hagihara
Journal:  Mol Clin Oncol       Date:  2016-10-26

9.  Beyond JAK-STAT: novel therapeutic targets in Ph-negative MPN.

Authors:  Aaron T Gerds
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2019-12-06

Review 10.  Efficacy and safety of ruxolitinib in the treatment of patients with myelofibrosis.

Authors:  Cecilia Arana Yi; Constantine S Tam; Srdan Verstovsek
Journal:  Future Oncol       Date:  2015       Impact factor: 3.404

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