Acute Myeloid Leukemia: analysis of epidemiological profile and survival rate

Abstract Objective: To describe the epidemiological profile and the survival rate of patients with acute myeloid leukemia (AML) in a state reference pediatric hospital. Method: Clinical-epidemiological, observational, retrospective, descriptive study. The study included new cases of patients with AM...

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Veröffentlicht in:Jornal de pediatria 2016-06, Vol.92 (3), p.283-289
Hauptverfasser: Mariana Cardoso de Lima, Denise Bousfield da Silva, Ana Paula Ferreira Freund, Juliana Shmitz Dacoregio, Tatiana El Jaick Bonifácio Costa, Imaruí Costa, Daniel Faraco, Maurício Laerte Silva
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Sprache:eng
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Zusammenfassung:Abstract Objective: To describe the epidemiological profile and the survival rate of patients with acute myeloid leukemia (AML) in a state reference pediatric hospital. Method: Clinical-epidemiological, observational, retrospective, descriptive study. The study included new cases of patients with AML, diagnosed between 2004 and 2012, younger than 15 years. Results: Of the 51 patients studied, 84% were white; 45% were females and 55%, males. Regarding age, 8% were younger than 1 year, 47% were aged between 1 and 10 years, and 45% were older than 10 years. The main signs/symptoms were fever (41.1%), asthenia/lack of appetite (35.2%), and hemorrhagic manifestations (27.4%). The most affected extra-medullary site was the central nervous system (14%). In 47% of patients, the white blood cell (WBC) count was below 10,000/mm3 at diagnosis. The minimal residual disease (MRD) was less than 0.1%, on the 15th day of treatment in 16% of the sample. Medullary relapse occurred in 14% of cases. When comparing the bone marrow MRD with the vital status, it was observed that 71.42% of the patients with type M3 AML were alive, as were 54.05% of those with non-M3 AML. The death rate was 43% and the main proximate cause was septic shock (63.6%). Conclusions: In this study, the majority of patients were male, white, and older than 1 year. Most patients with WBC count
ISSN:1678-4782
DOI:10.1016/j.jped.2015.08.008