ABSTRACT
UNLABELLED: Prognosis of myelodysplastic syndromes (MDS) is an area of ongoing interest. Identification of patients with poor outcome in the categories of lower risk disease is critical. In this study, we classify a cohort of 332 lower risk MDS into 3 groups with differences in survival and risk for leukemic progression that could drive treatment approaches to improve prognosis in a fraction of these patients. BACKGROUND: Prognosis of MDS and particularly in patients categorized as lower risk (< 10% blasts or low and intermediate-1 International Prognostic Scoring System [IPSS]) is very heterogeneous and includes patients with very different outcomes with current scoring systems. Recently, a new cytogenetic classification has been proposed for the revised IPSS in predicting the outcome for MDS. PATIENTS AND METHODS: To evaluate the prognostic significance of multiple variables for survival and risk of progression to acute myeloid leukemia, we analyzed baseline characteristics of 332 lower risk MDS patients within the lower risk cytogenetic categories by IPSS and the recent proposal for the new cytogenetic classification. RESULTS: In multivariate analysis, severity of cytopenias, age > 60 years, bone marrow blasts (5%-9%) and transfusion dependency significantly influenced outcome. The combination of these variables allowed development of a model which categorizes patients in 3 different groups with median survival of 95, 44, and 13 months for groups 1, 2, and 3, respectively (P < .001). In addition, this score also stratified patients for their risk for leukemic progression, estimated at 2 years in 3.1%, 7.6%, and 21.3% for each group (P = .024). CONCLUSION: Although karyotype remains the main prognostic factor in MDS, the current study identifies clinical parameters predicting outcome among patients with the better cytogenetic profile. Degree of cytopenias, blasts 5%-9% and transfusion dependence might identify a subset of patients within the nonadverse karyotype, in which early or more aggressive approaches could possibly be required to improve survival or prevent disease progression.
Subject(s)
Bone Marrow Cells/pathology , Chromosome Aberrations , Leukemia, Myeloid, Acute/etiology , Leukemia, Myeloid, Acute/mortality , Myelodysplastic Syndromes/diagnosis , Myelodysplastic Syndromes/mortality , Adolescent , Adult , Aged , Aged, 80 and over , Disease Progression , Female , Humans , Karyotype , Male , Middle Aged , Prognosis , Young AdultSubject(s)
CD56 Antigen/metabolism , Leukemia-Lymphoma, Adult T-Cell/diagnosis , Myeloid Progenitor Cells/classification , T-Lymphocyte Subsets/classification , Adolescent , Adult , CD56 Antigen/analysis , Cell Lineage , Cell Transformation, Neoplastic , Child , Child, Preschool , Female , Hematopoietic Stem Cells/classification , Humans , Immunophenotyping , Infant , Leukemia-Lymphoma, Adult T-Cell/drug therapy , Leukemia-Lymphoma, Adult T-Cell/pathology , Male , Prognosis , Remission Induction , Survival AnalysisSubject(s)
Adenocarcinoma/complications , Bone Marrow/pathology , Neoplasms, Unknown Primary/diagnosis , Purpura, Thrombotic Thrombocytopenic/etiology , Stomach Neoplasms/complications , Adult , Fatal Outcome , Fever/etiology , Humans , Male , Necrosis , Neoplasms, Unknown Primary/complications , Neoplasms, Unknown Primary/pathology , Pain/etiologyABSTRACT
Descreve os resultados de estudo epidemiológico da evoluçäo da cólera em Moçambique no período de 1973 a 1992, objetivando analisar a influência dos fatores socioeconômicos e ecológicos, de um país em guerra, na propagaçäo da doença. Utiliza informaçöes relativas à incidência e letalidade da cólera, relacionando-as com a taxa de crescimento médio anual da populaçäo das cidades e precipitaçäo pluvial. Analisa também o abastecimento de àgua potável, o saneamento do meio e higiene alimentar. Encontrou-se uma taxa elevada de crescimento médio anual da populaçäo nos centros urbanos, tendo uma correlaçäo linear direta com a incidência da coléra. A seca ocorrida em 1991-1992 também exerceu papel importante no aumento e propagaçäo da doença. A cólera tem tido padräo endêmico-epidêmico, determinado por: a) crescimento populacional urbano descontrolado, provocado pela guerra, b) reduçäo da qualidade das condiçöes higiênico-sanitárias nos centros urbanos; c) comercializaçäo de produtos alimentares sem o devido controle sanitário; d) a seca