Literature DB >> 16423393

Classification and scoring systems in myelodysplastic syndromes: a retrospective analysis of 311 patients.

I Navarro1, M A Ruiz, A Cabello, R Collado, R Ferrer, J Hueso, J Martinez, A Miguel, M T Orero, P Pérez, A Nolasco, F Carbonell.   

Abstract

The main objective of this study was to evaluate the role of the recent World Health Organization (WHO) classification for assessing prognosis in patients with myelodysplastic syndromes (MDS). To this effect, we analyzed the prognostic impact of the WHO and French-American-British (FAB) morphologic classifications and of four different scoring systems in a series of 311 patients with primary MDS diagnosed between October 1990 and June 2001. Both the FAB and WHO classifications identified groups with different prognoses (p<0.0001), those presenting refractory anemia (RA) and refractory anemia with ringed sideroblasts (RARS) showing the best prognosis. The WHO classification subdivided RA into RA with only red cell dysplasia, and refractory cytopenia with multilineage dysplasia (RCMD), and RARS into RARS plus refractory cytopenia with multilineage dysplasia and ringed sideroblast (RCMD-RS). In our population, we have shown that the two subtypes characterized by dysplasia affecting exclusively the erythroid population (RA and RARS) have a better prognosis, with a median survival of 122.2 and 81.9 months, respectively, than those with multilineage dysplasia (RCMD and RCMD-RS) with a median survival of 32.3 and 43.2 months, respectively. There were no significant differences in median survival comparing RA with RAS (p<0.95), or comparing RCMD with RSCMD (p<0.97). Besides, the four scoring systems discriminated our MDS patients in terms of survival, and an increase in prognostic capacity was achieved on adding the score to the morphological classifications. Risk scoring had a greater prognostic impact than the FAB and WHO classifications. Prognostic scoring systems may be an important tool for risk stratification in hematological practice, and add significance to morphological classification. Combined application of the WHO classification and score system is useful for improving the identification of patients with a poorer prognosis. The WHO classification establishes more homogeneous subcategories than the FAB classification and is also able to identify groups with different prognoses.

Entities:  

Mesh:

Year:  2006        PMID: 16423393     DOI: 10.1016/j.leukres.2005.11.015

Source DB:  PubMed          Journal:  Leuk Res        ISSN: 0145-2126            Impact factor:   3.156


  7 in total

1.  A prospective multicenter observational study of decitabine treatment in Korean patients with myelodysplastic syndrome.

Authors:  Je-Hwan Lee; Jun Ho Jang; Jinny Park; Seonyang Park; Young-Don Joo; Yeo-Kyeoung Kim; Hoon-Gu Kim; Chul Won Choi; Sung-Hyun Kim; Seong Kyu Park; Eunkyung Park; Yoo Hong Min
Journal:  Haematologica       Date:  2011-06-09       Impact factor: 9.941

2.  Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts.

Authors:  E Papaemmanuil; M Cazzola; J Boultwood; L Malcovati; P Vyas; D Bowen; A Pellagatti; J S Wainscoat; E Hellstrom-Lindberg; C Gambacorti-Passerini; A L Godfrey; I Rapado; A Cvejic; R Rance; C McGee; P Ellis; L J Mudie; P J Stephens; S McLaren; C E Massie; P S Tarpey; I Varela; S Nik-Zainal; H R Davies; A Shlien; D Jones; K Raine; J Hinton; A P Butler; J W Teague; E J Baxter; J Score; A Galli; M G Della Porta; E Travaglino; M Groves; S Tauro; N C Munshi; K C Anderson; A El-Naggar; A Fischer; V Mustonen; A J Warren; N C P Cross; A R Green; P A Futreal; M R Stratton; P J Campbell
Journal:  N Engl J Med       Date:  2011-09-26       Impact factor: 91.245

3.  Splicing factor SF3B1 mutations and ring sideroblasts in myelodysplastic syndromes: a Brazilian cohort screening study.

Authors:  Flávia Sacilotto Donaires; Felipe Martelli; Raquel de Melo Alves-Paiva; Silvia Maria Meira Magalhães; Ronald Feitosa Pinheiro; Rodrigo Tocantins Calado
Journal:  Rev Bras Hematol Hemoter       Date:  2016-07-04

Review 4.  Prognostic Markers of Myelodysplastic Syndromes.

Authors:  Yuliya Andreevna Veryaskina; Sergei Evgenievich Titov; Igor Borisovich Kovynev; Tatiana Ivanovna Pospelova; Igor Fyodorovich Zhimulev
Journal:  Medicina (Kaunas)       Date:  2020-07-27       Impact factor: 2.430

5.  Decitabine for Treatment of Myelodysplastic Syndromes in Chinese Patients: An Open-Label, Phase-3b Study.

Authors:  Depei Wu; Xin Du; Jie Jin; Zhijian Xiao; Zhixiang Shen; Zonghong Shao; Xiao Li; Xiaojun Huang; Ting Liu; Li Yu; Jianyong Li; Baoan Chen; Guangsheng He; Zhen Cai; Hongchuang Liang; Jigang Li; Changgeng Ruan
Journal:  Adv Ther       Date:  2015-11-14       Impact factor: 3.845

6.  Acquired Elliptocytosis as a Manifestation of Myelodysplastic Syndrome Associated with Deletion of Chromosome 20q.

Authors:  Sukesh Manthri; Naresh K Vasireddy; Sindhura Bandaru; Swati Pathak
Journal:  Case Rep Hematol       Date:  2018-02-01

7.  Acquired Elliptocytosis as a Manifestation of Myelodysplastic Syndrome with Ring Sideroblasts and Multilineage Dysplasia.

Authors:  Jacob D Kjelland; Denis M Dwyre; Brian A Jonas
Journal:  Case Rep Hematol       Date:  2017-10-11
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.