The prognostic effect on childhood acute lymphoblastic leukemia of CD34+CD38- expressed in leukemia cells

Jiou Zhao1, Yun Wang2, Min Zhou3

  • 1Jiangsu Food and Pharmaceutical Science College, Jiangsu, People's Republic of China.

Insights

CD34 and CD38 expression levels in childhood acute lymphoblastic leukemia do not affect overall survival. However, CD34-positive, CD38-negative leukemia cells may indicate a poorer prognosis in these young patients.

Area of Science:

  • Pediatric Oncology
  • Hematology
  • Immunophenotyping

Background:

  • Acute lymphoblastic leukemia (ALL) is the most common childhood malignancy.
  • CD34 and CD38 are cell surface markers expressed on normal and leukemia cells.
  • Limited data exists on the prognostic significance of CD34 and CD38 expression in pediatric ALL.

Purpose of the Study:

  • To investigate the prognostic impact of CD34+CD38- leukemia cells in children diagnosed with ALL.
  • To analyze the association between CD34 and CD38 expression and patient outcomes.

Main Methods:

  • Children with newly diagnosed ALL were enrolled between January 2014 and January 2019.
  • Patients were categorized into CD34+ and CD34- groups, with the CD34+ group further divided into CD34+CD38- and CD34+CD38+ subgroups.
  • Clinical features, treatment outcomes, overall survival (OS), and event-free survival (EFS) were tracked and compared.

Main Results:

  • No significant difference in OS or EFS was observed between CD34+ and CD34- groups.
  • The CD34+CD38- group showed a significantly worse OS (P=0.048) and higher recurrence rate (P=0.025) compared to the CD34+CD38+ group.
  • After propensity score matching, the recurrence rate remained significantly higher in the CD34+CD38- group (P<0.001).

Conclusions:

  • CD34 expression alone does not predict prognosis in pediatric ALL.
  • The presence of CD34+CD38- leukemia cells is associated with a poor prognosis, including increased recurrence rates.
  • Further research into the role of specific immunophenotypic markers like CD34 and CD38 is crucial for refining risk stratification in pediatric ALL.
Abstract

Related Concept Videos