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Primary myelofibrosis: risk stratification by IPSS identifies patients with poor clinical outcome
OBJECTIVES: To evaluate whether risk scores used to classify patients with primary myelofibrosis and JAK-2 V617F mutation status can predict clinical outcome. METHODS: A review of clinical and laboratory data from 74 patients with primary myelofibrosis diagnosed between 1992 and 2011. The IPSS and L...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3611898/ https://www.ncbi.nlm.nih.gov/pubmed/23644853 http://dx.doi.org/10.6061/clinics/2013(03)OA09 |
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author | Benites, Bruno Deltreggia Lima, Carolina Silva Costa Lorand-Metze, Irene Delamain, Marcia Torresan Oliveira, Gislaine Borba de Almeida, Daiane de Souza, Carmino Antonio Vassallo, Jose Pagnano, Katia Borgia Barbosa |
author_facet | Benites, Bruno Deltreggia Lima, Carolina Silva Costa Lorand-Metze, Irene Delamain, Marcia Torresan Oliveira, Gislaine Borba de Almeida, Daiane de Souza, Carmino Antonio Vassallo, Jose Pagnano, Katia Borgia Barbosa |
author_sort | Benites, Bruno Deltreggia |
collection | PubMed |
description | OBJECTIVES: To evaluate whether risk scores used to classify patients with primary myelofibrosis and JAK-2 V617F mutation status can predict clinical outcome. METHODS: A review of clinical and laboratory data from 74 patients with primary myelofibrosis diagnosed between 1992 and 2011. The IPSS and Lille scores were calculated for risk stratification and correlated with overall survival. RESULTS: A V617F JAK2 mutation was detected in 32 cases (47%), with no significant correlation with overall survival. The patients were classified according to the scores: Lille - low, 53 (73.%); intermediate, 13 (18%); and high, 5 (7%); and IPSS – low, 15 (26%); intermediate-1, 23 (32%); intermediate-2, 19 (26%); and high, 15 (31%). Those patients presenting a higher risk according to the IPSS (high and intermediate-2) had a significantly shorter overall survival relative to the low risk groups (intermediate-1 and low) (p = 0.02). CONCLUSIONS: These results emphasize the importance of the IPSS prognostic score for risk assessment in predicting the clinical outcome of primary myelofibrosis patients. |
format | Online Article Text |
id | pubmed-3611898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo |
record_format | MEDLINE/PubMed |
spelling | pubmed-36118982013-04-05 Primary myelofibrosis: risk stratification by IPSS identifies patients with poor clinical outcome Benites, Bruno Deltreggia Lima, Carolina Silva Costa Lorand-Metze, Irene Delamain, Marcia Torresan Oliveira, Gislaine Borba de Almeida, Daiane de Souza, Carmino Antonio Vassallo, Jose Pagnano, Katia Borgia Barbosa Clinics (Sao Paulo) Clinical Science OBJECTIVES: To evaluate whether risk scores used to classify patients with primary myelofibrosis and JAK-2 V617F mutation status can predict clinical outcome. METHODS: A review of clinical and laboratory data from 74 patients with primary myelofibrosis diagnosed between 1992 and 2011. The IPSS and Lille scores were calculated for risk stratification and correlated with overall survival. RESULTS: A V617F JAK2 mutation was detected in 32 cases (47%), with no significant correlation with overall survival. The patients were classified according to the scores: Lille - low, 53 (73.%); intermediate, 13 (18%); and high, 5 (7%); and IPSS – low, 15 (26%); intermediate-1, 23 (32%); intermediate-2, 19 (26%); and high, 15 (31%). Those patients presenting a higher risk according to the IPSS (high and intermediate-2) had a significantly shorter overall survival relative to the low risk groups (intermediate-1 and low) (p = 0.02). CONCLUSIONS: These results emphasize the importance of the IPSS prognostic score for risk assessment in predicting the clinical outcome of primary myelofibrosis patients. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2013-03 /pmc/articles/PMC3611898/ /pubmed/23644853 http://dx.doi.org/10.6061/clinics/2013(03)OA09 Text en Copyright © 2013 Hospital das Clínicas da FMUSP http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Science Benites, Bruno Deltreggia Lima, Carolina Silva Costa Lorand-Metze, Irene Delamain, Marcia Torresan Oliveira, Gislaine Borba de Almeida, Daiane de Souza, Carmino Antonio Vassallo, Jose Pagnano, Katia Borgia Barbosa Primary myelofibrosis: risk stratification by IPSS identifies patients with poor clinical outcome |
title | Primary myelofibrosis: risk stratification by IPSS identifies patients with poor clinical outcome |
title_full | Primary myelofibrosis: risk stratification by IPSS identifies patients with poor clinical outcome |
title_fullStr | Primary myelofibrosis: risk stratification by IPSS identifies patients with poor clinical outcome |
title_full_unstemmed | Primary myelofibrosis: risk stratification by IPSS identifies patients with poor clinical outcome |
title_short | Primary myelofibrosis: risk stratification by IPSS identifies patients with poor clinical outcome |
title_sort | primary myelofibrosis: risk stratification by ipss identifies patients with poor clinical outcome |
topic | Clinical Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3611898/ https://www.ncbi.nlm.nih.gov/pubmed/23644853 http://dx.doi.org/10.6061/clinics/2013(03)OA09 |
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