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In Vitro Differentiation of Mouse Granulocyte-macrophage-colony-stimulating Factor GM-CSF-producing T Helper THGM Cells
Published on: September 10, 2018
Early versus delayed administration of granulocyte-colony stimulating factor following chemotherapy in pediatric
Deema Al-Momani1, Wiam Al-Qasem1, Rawan Kasht1
1Department of Pharmacy, King Hussein Cancer Center, Amman, Jordan.
Insights
Initiating granulocyte-colony stimulating factor (G-CSF) on day 3 post-chemotherapy, compared to day 1, did not increase febrile neutropenia hospitalizations in pediatric Ewing sarcoma patients. Delaying G-CSF reduced chemotherapy interruptions.
Area of Science:
- Pediatric Oncology
- Hematology
- Pharmacology
Background:
- Optimal timing for granulocyte-colony stimulating factor (G-CSF) initiation post-chemotherapy in pediatric patients remains undefined.
- Ewing sarcoma treatment involves chemotherapy, necessitating management of neutropenia.
- G-CSF is crucial for mitigating chemotherapy-induced neutropenia.
Purpose of the Study:
- To compare the safety and efficacy of initiating G-CSF on day 1 versus day 3 post-chemotherapy.
- To evaluate the impact of G-CSF timing on febrile neutropenia and chemotherapy delays in pediatric Ewing sarcoma patients.
Main Methods:
- Retrospective study of pediatric patients with Ewing sarcoma receiving G-CSF.
- Comparison of outcomes before (day 1 initiation) and after (day 3 initiation) a protocol change.
- Key outcomes assessed: febrile neutropenia requiring hospitalization, hospital stay duration, and chemotherapy delay.
Main Results:
- No significant difference in febrile neutropenia hospitalizations or length of stay between day 1 and day 3 G-CSF initiation.
- Significantly fewer chemotherapy delays occurred when G-CSF was initiated on day 3 compared to day 1.
- 250 cycles with day 1 G-CSF and 221 cycles with day 3 G-CSF were analyzed.
Conclusions:
- Initiating G-CSF on day 3 post-chemotherapy is comparable to day 1 for preventing febrile neutropenia hospitalizations in pediatric Ewing sarcoma.
- Delayed G-CSF initiation (day 3) effectively reduces chemotherapy delays due to neutropenia.
- Further research with larger cohorts is needed to confirm the long-term impact of delayed G-CSF initiation.
Background:
The optimal timing of initiating granulocyte-colony stimulating factor following chemotherapy in pediatric patients has not been clearly defined. This study aimed to compare the administration of granulocyte-colony stimulating factor on day 1 versus day 3 postchemotherapy in pediatric patients with Ewing sarcoma.
Method:
A retrospective study of pediatric patients with Ewing sarcoma who received granulocyte-colony stimulating factor following chemotherapy between January 2016 and September 2018 at a comprehensive cancer center. The institution's chemotherapy protocol for Ewing sarcoma was modified in April 2017 to include granulocyte-colony stimulating factor initiation on day 3 instead of day 1 post-chemotherapy. Febrile neutropenia requiring hospitalization, duration of hospital stay, and chemotherapy delay were compared for patients before and after the protocol change.
Results:
Over the study period, 250 cycles were evaluated with day 1 granulocyte-colony stimulating factor and 221 cycles with day 3 granulocyte-colony stimulating factor. There were no differences between the day 1 and day 3 groups in the number of cycles associated with Febrile neutropenia requiring hospitalization (34 vs. 19, p = 0.086), and the length of Febrile neutropenia-related hospitalization (mean 4 ± 2.1 vs. 4.6 ± 1.8, p = 0.123). However, delay in chemotherapy due to neutropenia was reported in significantly more cycles in the day 1 group, compared to the day 3 group (37 vs. 16, p = 0.01).
Conclusions:
Febrile neutropenia resulting in hospital admission and the length of hospital stay was not different between pediatric patients with Ewing sarcoma who received granulocyte-colony stimulating factor on day 1 or day 3 post-chemotherapy. Chemotherapy delay due to neutropenia was higher in patients who received granulocyte-colony stimulating factor on day 1. Larger studies are required to fully determine the impact of delayed initiation of granulocyte-colony stimulating factor.
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