The effect of granulocyte colony-stimulating factors on survival parameters in pediatric patients with acute

Sibel Akpınar Tekgunduz1, Ali Aycicek1, Cengiz Bayram1

  • 1Department of Pediatric Hematology and Oncology, Basaksehir Cam ve Sakura City Hospital, Istanbul, Turkey.

Insights

Granulocyte colony-stimulating factors (G-CSFs) did not impact relapse-free or overall survival in pediatric acute lymphoblastic leukemia (ALL) patients. This study found no significant difference in outcomes between G-CSF treated and untreated groups.

Area of Science:

  • Pediatric Oncology
  • Hematology
  • Clinical Pharmacology

Background:

  • Limited data exists on granulocyte colony-stimulating factors (G-CSFs) use in pediatric acute lymphoblastic leukemia (ALL).
  • G-CSFs are often used to mitigate neutropenia and treatment delays in chemotherapy protocols.

Purpose of the Study:

  • To evaluate the impact of G-CSF on relapse-free survival (RFS) and overall survival (OS) in pediatric ALL patients.
  • To analyze survival outcomes based on G-CSF administration during treatment.

Main Methods:

  • Retrospective analysis of 358 newly diagnosed pediatric ALL patients treated between April 2012 and April 2020.
  • Patients were divided into two groups: G-CSF positive (n=245, treated April 2012-December 2016) and G-CSF negative (n=113, treated after December 2016).
  • Uniform treatment protocols were applied at a single institution.

Main Results:

  • No significant difference in estimated mean relapse-free survival between G-CSF+ (106.5 months) and G-CSF- (82 months) groups (p=0.794).
  • Overall survival rates were also similar, with 111.4 months for G-CSF+ and 85 months for G-CSF- groups (p=0.431).
  • These findings suggest G-CSF administration did not influence survival outcomes.

Conclusions:

  • G-CSF use during the treatment of pediatric ALL did not demonstrate a significant effect on relapse rates.
  • Overall survival in pediatric ALL patients was not altered by the administration of G-CSF.
  • Further research may be warranted to explore specific subgroups or alternative indications for G-CSF in pediatric ALL.
Abstract