Blood Res.  2014 Mar;49(1):29-35. 10.5045/br.2014.49.1.29.

Childhood acute lymphoblastic leukemia with hyperleukocytosis at presentation

Affiliations
  • 1Department of Pediatrics, Pusan National University College of Medicine, Busan, Korea. limyt@pusan.ac.kr

Abstract

BACKGROUND
Hyperleukocytosis caused by acute lymphoblastic leukemia (ALL) is associated with early morbidity and mortality due to hyperviscosity arising from the excessive number of leukocytes.This study was designed to assess the incidence of hyperleukocytosis, survival outcomes, and adverse features among pediatric ALL patients with hyperleukocytosis.
METHODS
Between January 2001 and December 2010, 104 children with previously untreated ALL were enrolled at the Pusan National University Hospital. All of them were initially stratified based on the National Cancer Institute (NCI) risk; 48 (46.2%) were diagnosed with high-risk ALL. The medical charts of these patients were retrospectively reviewed.
RESULTS
Twenty (19.2%) of the 104 children with ALL had initial leukocyte counts of >100x10(9)/L, and 11 patients had a leukocyte count of >200x10(9)/L. Male gender, T-cell phenotype, and massive splenomegaly were positively associated with hyperleukocytosis. Common early complications during induction therapy included renal dysfunction, and central nervous system hemorrhage. The complete remission (CR) rate for the pediatric ALL patients with hyperleukocytosis (94.1%) was similar to the overall CR rate (95.6%). The estimated 3-year event free survival (EFS) and overall survival of ALL children with hyperleukocytosis were 75.0% and 81.2%, respectively. However, patients with initial leukocyte counts >200x10(9)/L had a lower EFS than those with initial leukocyte counts 100-200x109/L (63.6% vs. 100%; P=0.046).
CONCLUSION
The outcome of pediatric ALL cases with an initial leukocyte count >200x10(9)/L was very poor, probably due to early toxicity-related death during induction therapy.

Keyword

Pediatric acute lymphoblastic leukemia; Hyperleukocytosis; Central nervous system hemorrhage

MeSH Terms

Busan
Central Nervous System
Child
Disease-Free Survival
Hemorrhage
Humans
Incidence
Leukocyte Count
Male
Mortality
National Cancer Institute (U.S.)
Phenotype
Precursor Cell Lymphoblastic Leukemia-Lymphoma*
Retrospective Studies
Splenomegaly
T-Lymphocytes

Figure

  • Fig. 1 Kaplan-Meier estimates of event free survival of children with high-risk ALL (P=0.04).

  • Fig. 2 Kaplan-Meier estimate of overall survival of children with high-risk ALL (P=0.09).


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