Literature DB >> 20425325

Who is WHO in myelodysplastic syndromes? Clinical implications of the WHO classification.

Rami S Komrokji1, John M Bennett.   

Abstract

Myelodysplastic syndromes (MDS) are a heterogeneous group of neoplastic clonal stem cell diseases characterized by dysplastic morphologic features with a varying percentage of leukemic blasts and clinical bone marrow failure. The French-American-British (FAB) system served as the gold standard of MDS classification for more than two decades. The World Health Organization (WHO) classification, built on the backbone of the FAB classification, is an attempt to further improve the prognostic value of MDS classification as well as to establish its clinical utility as a tool to select different treatments. In this article we highlight the major differences between the FAB classification and the WHO MDS classification. We discuss in more detail the experience of using the new WHO classification since its publication and review the studies that have tried to validate the prognostic value of the new classification or apply it to predict clinical responses to various treatments.

Entities:  

Mesh:

Year:  2006        PMID: 20425325     DOI: 10.1007/s11899-006-0011-x

Source DB:  PubMed          Journal:  Curr Hematol Malig Rep        ISSN: 1558-8211            Impact factor:   3.952


  24 in total

1.  Re-evaluation of refractory anemia with excess blasts in transformation.

Authors:  K Ohyashiki; J Nishimaki; N Shoji; K Miyazawa; Y Kimura; J H Ohyashiki
Journal:  Leuk Res       Date:  2001-11       Impact factor: 3.156

2.  Prognostic factors and life expectancy in myelodysplastic syndromes classified according to WHO criteria: a basis for clinical decision making.

Authors:  Luca Malcovati; Matteo Giovanni Della Porta; Cristiana Pascutto; Rosangela Invernizzi; Marina Boni; Erica Travaglino; Francesco Passamonti; Luca Arcaini; Margherita Maffioli; Paolo Bernasconi; Mario Lazzarino; Mario Cazzola
Journal:  J Clin Oncol       Date:  2005-09-26       Impact factor: 44.544

3.  Preleukemia. The hematologic syndrome preceding acute leukemia.

Authors:  M I Saarni; J W Linman
Journal:  Am J Med       Date:  1973-07       Impact factor: 4.965

4.  Validation of the WHO proposals for a new classification of primary myelodysplastic syndromes: a retrospective analysis of 1600 patients.

Authors:  U Germing; N Gattermann; C Strupp; M Aivado; C Aul
Journal:  Leuk Res       Date:  2000-12       Impact factor: 3.156

Review 5.  The World Health Organization (WHO) classification of the myeloid neoplasms.

Authors:  James W Vardiman; Nancy Lee Harris; Richard D Brunning
Journal:  Blood       Date:  2002-10-01       Impact factor: 22.113

6.  The WHO classification of MDS does make a difference.

Authors:  Robert B Howe; Anna Porwit-MacDonald; Robert Wanat; Ramin Tehranchi; Eva Hellström-Lindberg
Journal:  Blood       Date:  2003-12-18       Impact factor: 22.113

7.  A prognostic impact of separation of refractory cytopenia with multilineage dysplasia and 5q- syndrome from refractory anemia in primary myelodysplastic syndrome.

Authors:  Jaroslav Cermák; Kyra Michalová; Jana Brezinová; Zuzana Zemanová
Journal:  Leuk Res       Date:  2003-03       Impact factor: 3.156

8.  Factors influencing survival in myelodysplastic syndromes in a Brazilian population: comparison of FAB and WHO classifications.

Authors:  Irene Lorand-Metze; Mariana P Pinheiro; Elisangela Ribeiro; Erich V de Paula; Konradin Metze
Journal:  Leuk Res       Date:  2004-06       Impact factor: 3.156

9.  Proposals for the classification of the acute leukaemias. French-American-British (FAB) co-operative group.

Authors:  J M Bennett; D Catovsky; M T Daniel; G Flandrin; D A Galton; H R Gralnick; C Sultan
Journal:  Br J Haematol       Date:  1976-08       Impact factor: 6.998

Review 10.  The myelodysplastic syndromes: classification and prognosis.

Authors:  Rami Komrokji; John M Bennett
Journal:  Curr Hematol Rep       Date:  2003-05
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.