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Updated: Jun 6, 2026

Proliferation and Differentiation of Murine Myeloid Precursor 32D/G-CSF-R Cells
Published on: February 21, 2018
Myeloid growth factors as anti-infective measures in children with leukemia and lymphoma
Thomas Lehrnbecher1, Ursula Creutzig
1Pediatric Hematology and Oncology, Children's Hospital III, Johann Wolfgang Goethe-University, Theodor-Stern-Kai 7, Frankfurt, Germany. thomas.lehrnbecher@kgu.de
Insights
Hematopoietic growth factors like G-CSF and GM-CSF reduced neutropenia in pediatric leukemia and lymphoma patients but did not lower infection risk or improve survival. Caution is advised due to potential relapse risks.
Area of Science:
- Pediatric Hematology Oncology
- Hematopoietic Stem Cell Support
Background:
- Hematopoietic colony-stimulating factors (CSFs) are used in pediatric cancer treatment.
- Granulocyte (G)-CSF and granulocyte-macrophage (GM)-CSF are commonly administered CSFs.
Purpose of the Study:
- To evaluate the efficacy of G-CSF and GM-CSF in children with leukemia and lymphoma.
- To assess the impact of CSFs on neutropenia, infectious complications, and survival.
Main Methods:
- Analysis of clinical trial data in pediatric patients with leukemia and lymphoma.
- Comparison of outcomes between patients receiving CSFs and those not.
Main Results:
- G-CSF and GM-CSF reduced the duration and severity of neutropenia.
- Neither G-CSF nor GM-CSF significantly decreased infectious complications or improved overall survival.
- Antibiotic use and hospitalization rates appeared to decrease with CSF administration.
Conclusions:
- While CSFs mitigate neutropenia in pediatric leukemia/lymphoma patients, they do not reduce infection risk or improve survival.
- Guidelines recommend cautious use of hematopoietic growth factors in these populations due to potential relapse concerns.
Abstract:
Clinical trials in children treated for leukemia and lymphoma demonstrated that the hematopoietic colony-stimulating factors (CSFs) granulocyte (G) and granulocyte-macrophage (GM) CSFs ameliorate duration and depth of neutropenia, and also seem to decrease antibiotic usage and hospitalization. However, neither G-CSF nor GM-CSF significantly reduced the risk for infectious complications, such as febrile neutropenia or documented infections, or improved overall survival in these patient populations. Since it is unclear whether G- and GM-CSF may increase the risk for relapse in subgroups of patients with leukemia, guidelines recommend that hematopoietic growth factors should be used with caution in children with leukemia and lymphoma.
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