# Infections during AML induction chemotherapy in a contemporary cohort without fluoroquinolone prophylaxis

**Authors:** S. Ehrlich, J. Eufinger, N. Tahiri, V. Jurinovic, S. Mansournia, W. G. Kunz, J. Jung, T. Herold, M. Subklewe, V. Bücklein, M. von Bergwelt-Baildon, K. Spiekermann

PMC · DOI: 10.1007/s15010-025-02651-4 · Infection · 2025-10-01

## TL;DR

This study examines infections in AML patients undergoing chemotherapy without fluoroquinolone prophylaxis, finding that infections remain a major issue but multidrug resistance is rare.

## Contribution

The study provides real-world data on infection patterns in AML patients without fluoroquinolone prophylaxis, suggesting a need for individualized approaches and better diagnostics.

## Key findings

- Febrile episodes occurred in nearly all patients, with 29.8% being clinically documented infections.
- Gram-positive and Gram-negative bacteraemia were equally common, and multidrug resistance was rare.
- Infection-related 30-day mortality was 4.9%, with age and ICU admission as risk factors.

## Abstract

Recent advances in the treatment of acute myeloid leukemia (AML) and optimized supportive care have improved survival outcomes. However, infections during remission induction chemotherapy remain a leading cause of morbidity and mortality. While antifungal prophylaxis is standard, the role of routine antibacterial prophylaxis is increasingly debated due to adverse effects and resistance. This study aimed to characterize infectious complications in a real-world AML cohort receiving induction chemotherapy without routine antibacterial prophylaxis.

We retrospectively analyzed 103 adults with newly diagnosed AML who underwent intensive induction therapy at LMU University Hospital between January 2019 and December 2022. All patients received antifungal prophylaxis whereas antibacterial fluoroquinolone (FQ) prophylaxis was not administered. We assessed febrile episodes, clinically and microbiologically documented infections, ICU/IMC admissions, and 30-/90-day mortality.

Febrile episodes occurred in almost all patients. Clinically documented infections accounted for 29.8% and microbiologically confirmed infections for 22.9% of febrile events. Bacteraemia was evenly distributed between Gram-positive and Gram-negative pathogens; multidrug resistance was rare. Proven or probable invasive fungal infections occurred in 6.8% of patients. In 47.2% of cases, the cause of fever remained unknown. Infection-related 30-day mortality was 4.9%. Factors associated with increased 30-day mortality included age ≥ 65 years, ECOG ≥ 2, secondary AML, and ICU/IMC admission for infection.

Infections remain a major challenge during AML induction therapy. Our findings suggest that FQ prophylaxis should be reevaluated in this setting, focussing on a more individualized approach. In addition, novel diagnostic tools are urgently needed to enable earlier and more targeted infection management in this high-risk population.

The online version contains supplementary material available at 10.1007/s15010-025-02651-4.

## Linked entities

- **Diseases:** acute myeloid leukemia (MONDO:0015667)

## Full-text entities

- **Diseases:** fever (MESH:D005334), fungal infections (MESH:D009181), Bacteraemia (MESH:C531821), Febrile (MESH:D000071072), Infection (MESH:D007239), infectious complications (MESH:D003141), AML (MESH:D015470)
- **Chemicals:** FQ (MESH:D024841)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12864249/full.md

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Source: https://tomesphere.com/paper/PMC12864249