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Murine Model of Leukemia Relapse to Induction Chemotherapy for Acute Lymphoblastic Leukemia
Published on: October 17, 2025
Efficacy of fluoroquinolone prophylaxis during induction phase in children with acute lymphoblastic leukemia: a
Maria Clara Landivar1, Isabela Hartmann Rost2, Ana Carvalho Kilson3
1Universidad San Francisco de Quito, Quito, Ecuador. mclaralandivar@gmail.com.
Insights
Fluoroquinolone prophylaxis during induction chemotherapy for pediatric acute lymphoblastic leukemia (ALL) significantly lowers the risk of febrile neutropenia (FN) and bloodstream infections (BSI). This infection prevention strategy does not increase C. difficile risk, potentially improving treatment tolerance.
Area of Science:
- Pediatric Oncology
- Infectious Disease Prevention
- Hematology
Background:
- Febrile neutropenia (FN) and bloodstream infections (BSI) are significant causes of morbidity and mortality in pediatric acute lymphoblastic leukemia (ALL) patients undergoing induction chemotherapy.
- Previous studies on fluoroquinolone prophylaxis in this population have yielded inconsistent results, often limited by heterogeneous patient groups and a lack of focus on the induction phase.
Purpose of the Study:
- To systematically review and meta-analyze the efficacy of fluoroquinolone prophylaxis specifically during the induction chemotherapy phase for pediatric ALL.
- To assess the impact of fluoroquinolone prophylaxis on febrile neutropenia, bloodstream infections, Clostridioides difficile infection (CDI), and all-cause mortality (ACM).
Main Methods:
- A systematic literature search was conducted across PubMed, Scopus, and Cochrane databases for randomized controlled trials and observational studies.
- Random-effects meta-analysis was employed to pool data from 7 included studies involving 991 pediatric ALL patients.
- Primary outcome was FN; secondary outcomes included BSI, CDI, and ACM.
Main Results:
- Fluoroquinolone prophylaxis was associated with a significant reduction in the risk of FN (OR 0.44; 95% CI 0.33-0.59) and BSI (OR 0.50; 95% CI 0.32-0.81).
- No significant increase in the risk of Clostridioides difficile infection (CDI) (OR 0.43; 95% CI 0.00-42.30) or all-cause mortality (ACM) (OR 1.04; 95% CI 0.20-5.38) was observed.
- The protective effect on FN and BSI was consistent across different study designs.
Conclusions:
- Fluoroquinolone prophylaxis during induction chemotherapy for pediatric ALL effectively reduces the incidence of FN and BSI.
- The use of fluoroquinolones in this context does not appear to elevate the risk of CDI.
- Reducing infectious complications through fluoroquinolone prophylaxis may improve treatment tolerance and outcomes in pediatric ALL patients.
Abstract:
The role of infection prevention with fluoroquinolone prophylaxis specifically, during induction chemotherapy in pediatric acute lymphoblastic leukemia (ALL), remains unclear. Therefore, we conducted a systematic review and meta-analysis to assess its efficacy. PubMed, Scopus, and Cochrane databases were systematically searched for randomized controlled trials and observational studies. The main outcome was febrile neutropenia (FN) 26 and secondary outcomes were bloodstream infection (BSI), Clostridioides difficile infection (CDI) and all-cause mortality (ACM). A random-effects meta-analysis was conducted. We included 7 studies with 991 patients; 439 (44.3%) used fluoroquinolone prophylaxis, of whom 255 used levofloxacin and 184 used ciprofloxacin. The B-cell immunophenotype was the most frequent. Fluoroquinolone prophylaxis reduced the risk of FN (46.1% vs 64.9%; OR 0.44; 95% CI 0.33-0.59; I2 = 0%). Fluoroquinolone prophylaxis also significantly reduced the risk of BSI (OR 0.50; 95% CI 0.32-0.81; I2 = 0%). Risks of CDI (OR 0.43; 95% CI 0.00-42.30; I2 = 39.6%) and ACM (OR 1.04; 95% CI 0.20-5.38; I2 = 54.3%) were not significantly altered.
Conclusions:
Fluoroquinolone prophylaxis during induction chemotherapy for pediatric ALL significantly reduces FN and BSI without increasing C. difficile risk. While overall mortality is unchanged, reducing infectious morbidity may enhance treatment tolerance.
What Is Known:
• Febrile neutropenia and bloodstream infections are major causes of treatment-related morbidity and mortality during induction chemotherapy in pediatric acute lymphoblastic leukemia and fluoroquinolone prophylaxis has shown inconsistent results across studies. • Prior evidence suggests potential reduction in infectious complications, but is limited by heterogeneous populations and lack of analyses specific for induction phase.
What Is New:
• This systematic review and meta-analysis focused specifically on the induction phase of pediatric acute lymphoblastic leukemia and demonstrates that fluoroquinolone prophylaxis significantly reduces febrile neutropenia and bloodstream infections with consistent effect across study designs. • The study provides pooled estimate from an specific phase showing no clear increase in Clostridioides difficile infection, demonstrating the risk-benefit profile of fluoroquinolone prophylaxis.
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