Evidence map›Paper›PMID 40070813›Full record

ArticleOpen forum infectious diseases2025

Levofloxacin to Prevent Bacterial Infection in Patients With Acute Myeloid Leukemia Treated by Venetoclax and Azacitidine: A Toulouse-Bordeaux DATAML Registry Study.

Xavier Brousse, Nicolas Rasandisona, Emilie Bérard, Harmony Leroy, Karen Delavigne, Nathan Mottal, Suzanne Tavitian, Thibaut Leguay, Léopoldine Lapierre, Eric Delabesse and 14 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Xavier BrousseCHU Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.ORCID https://orcid.org/0000-0001-6345-9685
Nicolas RasandisonaService des Maladies infectieuses et tropicales, Toulouse University Hospital, Toulouse, France.
Emilie BérardCentre Hospitalier Universitaire de Toulouse, Service d'Epidémiologie, CERPOP, Inserm, Université Toulouse III Paul Sabatier, Toulouse, France.ORCID https://orcid.org/0000-0003-2451-5271
Harmony LeroyCHU Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.
Karen DelavigneService de Médecine Interne, Toulouse University Hospital, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.
Nathan MottalCHU Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.
Suzanne TavitianService d'Hématologie, Toulouse University Hospital, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.
Thibaut LeguayCHU Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.ORCID https://orcid.org/0000-0002-3123-4948
Léopoldine LapierreService d'Hématologie, Toulouse University Hospital, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.
Eric DelabesseLaboratoire d'Hématologie Biologique, Toulouse University Hospital, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.
Audrey BidetCHU Bordeaux, Laboratoire d'Hématologie Biologique, Bordeaux, France.ORCID https://orcid.org/0000-0003-0992-8377
Martin GauthierService d'Hématologie, Cahors Hospital, Cahors, France.
Diane LaraService d'Hématologie, Robert Boulin Hospital, Libourne, France.
Anne BanosService d'Hématologie, Côte Basque Hospital, Bayonne, France.
Jennifer GuiraudCHU Bordeaux, Laboratoire de Bactériologie, Bordeaux, France.
Pauline FlochLaboratoire de Bactériologie-Hygiène, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.
Leila GhenimService d'Hématologie, Rodez Hospital, Rodez, France.
Audrey SarryService d'Hématologie, Toulouse University Hospital, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.
Anne-Charlotte de GrandeCHU Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.
Clémentine BérangerCHU Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.
Christian RécherService d'Hématologie, Toulouse University Hospital, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.
Arnaud PigneuxCHU Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.
Sarah BertoliService d'Hématologie, Toulouse University Hospital, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.ORCID https://orcid.org/0000-0003-1084-2781
Pierre-Yves DumasCHU Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.ORCID https://orcid.org/0000-0003-0119-3548

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Antibiotic prophylaxis for patients with cancer remains a controversial issue and is not broadly recommended for hematological malignancies. The venetoclax (VEN) and azacitidine (AZA) combination allows for high rates of complete remission in acute myeloid leukemia (AML) but enhances the incidence of febrile neutropenia (FN) compared to AZA alone, making primary antibiotic prophylaxis a relevant question. Patients and Methods: Patients with AML who received VEN-AZA were selected from the DATAML registry to investigate the use of levofloxacin (LEVO) prophylaxis, administered at 500 mg/day from day 10 following the first course of VEN-AZA, until neutrophil recovery (>0.5 × 10 Results: A cohort of 258 patients was identified (median age 69.8 years, interquartile range 20.4-87.4), with 72 having received LEVO and 186 treated with standard of care (SOC). VEN-AZA was used for newly diagnosed AML in 52.7% of cases. FN occurred in 33.3% of LEVO patients versus 37.1% of SOC patients ( Conclusions: Levofloxacin as primary prophylaxis in patients with AML treated with VEN-AZA seems to decrease the rate of documented infections even if the incidence of FN was not significantly decreased. This prophylaxis shaped a different clinical and microbiological landscape without significant increase of antibiotic resistance.

Indexed as

acute myeloid leukemiaazacitidinefebrile neutropenialevofloxacinvenetoclax

Identifiers

PMID40070813
PMCPMC11894250

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.