C. Wanitpongpun, N. Teawtrakul, T. Lanamtieng, K. Chansung, Chittima Sirijeerachai, Worakamol Amampai, K. Sawanyawisuth
{"title":"Idarubicin and Ara-C treatment associated with fungal infection in acute leukemia patients with febrile neutropenia","authors":"C. Wanitpongpun, N. Teawtrakul, T. Lanamtieng, K. Chansung, Chittima Sirijeerachai, Worakamol Amampai, K. Sawanyawisuth","doi":"10.2174/2212697x08666211108095152","DOIUrl":null,"url":null,"abstract":"\n\n Acute leukemia with febrile neutropenia is at risk for infection. Fungal infection is a serious infection in this setting with a high mortality rate. There is limited data on clinical factors predictive of fungal infection in this setting. \n\n\n\n\n This study aimed to evaluate clinical predictive factors of fungal infection in acute leukemia patients with FN.\n\n\n\n\n This was a retrospective analytical study and included adult patients diagnosed with acute leukemia, who developed FN, and had positive culture on either bacterial or fungal infection. Predictors for fungal infection were calculated by using logistic regression analysis. A subgroup analysis in patients with acute myeloid leukemia (AML) was also performed. \n\n\n\n\n There were 94 patients who met the study criteria. Of those, 29 patients had positive culture for fungus (30.82%): categorized as Aspergillus (19 patients; 65.51%) and Candida (10 patients; 34.49%). The mortality rate was significantly higher in the fungal infection group than the bacterial infection group (24.14% vs 6.15%; p 0.031). There were six factors in the final model predictive of fungal infection with one independent predictor: treatment regimen of Idarubicin plus Ara-C with an adjusted odds ratio of 5.188 (95% CI of 1.386, 19.419). A subgroup analysis for fungal infection in patients with AML showed that only the treatment regimen of Idarubicin plus Ara-C was a significant factor. Its adjusted odds ratio was 5.138 (95% CI of 1.156, 24.467). \n\n\n\n\nTreatment with idarubicin and Ara-C may increase the risk of fungal infection in acute leukemia patients with FN.\n\n","PeriodicalId":91228,"journal":{"name":"Clinical cancer drugs","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical cancer drugs","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2212697x08666211108095152","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Acute leukemia with febrile neutropenia is at risk for infection. Fungal infection is a serious infection in this setting with a high mortality rate. There is limited data on clinical factors predictive of fungal infection in this setting.
This study aimed to evaluate clinical predictive factors of fungal infection in acute leukemia patients with FN.
This was a retrospective analytical study and included adult patients diagnosed with acute leukemia, who developed FN, and had positive culture on either bacterial or fungal infection. Predictors for fungal infection were calculated by using logistic regression analysis. A subgroup analysis in patients with acute myeloid leukemia (AML) was also performed.
There were 94 patients who met the study criteria. Of those, 29 patients had positive culture for fungus (30.82%): categorized as Aspergillus (19 patients; 65.51%) and Candida (10 patients; 34.49%). The mortality rate was significantly higher in the fungal infection group than the bacterial infection group (24.14% vs 6.15%; p 0.031). There were six factors in the final model predictive of fungal infection with one independent predictor: treatment regimen of Idarubicin plus Ara-C with an adjusted odds ratio of 5.188 (95% CI of 1.386, 19.419). A subgroup analysis for fungal infection in patients with AML showed that only the treatment regimen of Idarubicin plus Ara-C was a significant factor. Its adjusted odds ratio was 5.138 (95% CI of 1.156, 24.467).
Treatment with idarubicin and Ara-C may increase the risk of fungal infection in acute leukemia patients with FN.