G. Bahoush, E. Yazdi, S. Ansari, Arjm, P. Vossough
{"title":"Identification of Children with Acute Lymphoblastic Leukemia at Low Risk for Tumor Lysis Syndrome","authors":"G. Bahoush, E. Yazdi, S. Ansari, Arjm, P. Vossough","doi":"10.4172/2155-9864.1000318","DOIUrl":null,"url":null,"abstract":"Purpose: We determined the prevalence and predictors of TLS in children with acute lymphoblastic leukemia to develop a sensitive prediction rule to identify low risk patients. \nMethods: Predictors of TLS were determined in 160 childern with ALL, using univariate and multiple logistic regression analyses. Results: TLS was diagnosed in 41 cases. Univariate analysis showed splenomegaly, mediastinal mass, T-cell phenotype, central nervous system involvement, lactate dehydrogenase ≥2000 U/L, and white blood count (WBC) ≥20 × 109 /L (P<0.001) were predictors of TLS in these cases. Multiple regression analysis of variables identified CNS and renal involvement, mediastinal mass, and initial WBC ≥ 20 × 109 /L as independent predictors of TLS. \nConclusions: The above predictors could evaluate the risk of TLS in hematologic malignancies before initiative chemotherapy. Finding a model of independent factors to define a group of ALL children at low risk of TLS could be used to prevent cost of prophylactic treatment modalities.","PeriodicalId":182392,"journal":{"name":"Journal of Blood Disorders and Transfusion","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2015-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Blood Disorders and Transfusion","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2155-9864.1000318","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 8
Abstract
Purpose: We determined the prevalence and predictors of TLS in children with acute lymphoblastic leukemia to develop a sensitive prediction rule to identify low risk patients.
Methods: Predictors of TLS were determined in 160 childern with ALL, using univariate and multiple logistic regression analyses. Results: TLS was diagnosed in 41 cases. Univariate analysis showed splenomegaly, mediastinal mass, T-cell phenotype, central nervous system involvement, lactate dehydrogenase ≥2000 U/L, and white blood count (WBC) ≥20 × 109 /L (P<0.001) were predictors of TLS in these cases. Multiple regression analysis of variables identified CNS and renal involvement, mediastinal mass, and initial WBC ≥ 20 × 109 /L as independent predictors of TLS.
Conclusions: The above predictors could evaluate the risk of TLS in hematologic malignancies before initiative chemotherapy. Finding a model of independent factors to define a group of ALL children at low risk of TLS could be used to prevent cost of prophylactic treatment modalities.