» Articles » PMID: 16186598

Prognostic Factors and Life Expectancy in Myelodysplastic Syndromes Classified According to WHO Criteria: a Basis for Clinical Decision Making

Overview
Journal J Clin Oncol
Specialty Oncology
Date 2005 Sep 28
PMID 16186598
Citations 234
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: The aim of this study was to evaluate the prognostic value of the WHO proposal, to assess the role of the main prognostic factors in myelodysplastic syndromes (MDSs) classified into WHO subgroups, and to estimate mortality (standardized mortality ratio [SMR]) and life expectancy in these groups as a basis for clinical decision making.

Patients And Methods: Four hundred sixty-seven patients who were diagnosed as having de novo MDS at the Division of Hematology, University of Pavia (Pavia, Italy), between 1992 and 2002, were evaluated retrospectively for clinical and hematologic features at diagnosis, overall survival (OS), and progression to leukemia (leukemia-free survival).

Results: Significant differences in survival were noted between patients with refractory anemia (RA), refractory cytopenia with multilineage dysplasia, RA with excess blasts, type 1 (RAEB-1), and RAEB-2. The effect of demographic factors on OS was observed in MDS patients without excess blasts (age, P = .001; sex, P = .006), as in the general population. The mortality of RA patients 70 years or older did not differ significantly from that of the general population (SMR, 1.62; P = .06). Cytogenetics was the only International Prognostic Scoring System variable showing a prognostic value in MDS classified into WHO subgroups. Transfusion-dependent patients had a significantly shorter survival than patients who did not require transfusions (P < .001). Developing a secondary iron overload significantly affected the survival of transfusion-dependent patients (P = .003).

Conclusion: These data show that the WHO classification of MDSs has a relevant prognostic value. This classification, along with cytogenetics, might be useful in decisions regarding transplantation. MDS with isolated erythroid lineage dysplasia identifies a subset of truly low-risk patients, for whom a conservative approach is advisable.

Citing Articles

Safety and efficacy of luspatercept in treating anemia associated with myelodysplastic syndrome with ring sideroblasts in Asian patients who require red blood cell transfusions: a phase II bridging study.

Chang C, Suzuki T, Liang Y, Tong H, Usuki K, Liu Q Ther Adv Hematol. 2025; 16:20406207251321715.

PMID: 39991012 PMC: 11843707. DOI: 10.1177/20406207251321715.


The role of mitochondria in iron overload-induced damage.

Zhao Y, Yang M, Liang X J Transl Med. 2024; 22(1):1057.

PMID: 39587666 PMC: 11587765. DOI: 10.1186/s12967-024-05740-4.


Immunophenotyping myelodysplastic neoplasms: the role of flow cytometry in the molecular classification era.

Verigou E, Chatzilygeroudi T, Lazaris V, de Lastic A, Symeonidis A Front Oncol. 2024; 14:1447001.

PMID: 39544295 PMC: 11560873. DOI: 10.3389/fonc.2024.1447001.


Mesenchymal stem cells lineage and their role in disease development.

Xu Q, Hou W, Zhao B, Fan P, Wang S, Wang L Mol Med. 2024; 30(1):207.

PMID: 39523306 PMC: 11552129. DOI: 10.1186/s10020-024-00967-9.


Genome sequencing in the management of myelodysplastic syndromes and related disorders.

Cazzola M, Malcovati L Haematologica. 2024; 110(2):312-329.

PMID: 39445412 PMC: 11788631. DOI: 10.3324/haematol.2023.284947.