Evidence map›Paper›PMID 42053464›Full record

ArticleAntimicrobial agents and chemotherapy2026

A step toward defining optimal liposomal amphotericin B treatment duration in pulmonary mucormycosis: results from emulated trials.

Anne Coste, Olivier Paccoud, François Danion, Anne Conrad, Sylvain Poirée, Amandine Le Bourgeois, Claire Defrance, Valérie Letscher-Bru, Florent Morio, Thomas Gastinne and 21 more

Abstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

31 authors.

Anne CosteInfectious Diseases Department, La Cavale Blanche Hospital, Brest University Hospital, Brest, France.ORCID 0000-0002-9596-662X
Olivier Paccoud *Infectious Diseases Department, Necker-Enfants Malades Hospital, AP-HP, Paris, France.
François Danion *Infectious Diseases Department, Strasbourg University Hospital, Inserm UMR_S 1109, Immuno-rhumatologie Moléculaire, Strasbourg, France.
Anne ConradInfectious Diseases Department, Croix Rousse Hospital, Hospices Civils de Lyon, Lyon, France.
Sylvain PoiréeRadiology Department, Necker-Enfants Malades Hospital, AP-HP, Paris, France.
Amandine Le BourgeoisClinical Hematology Department, Nantes University Hospital, Nantes, France.
Claire DefranceRadiology Department, Nantes University Hospital, Nantes, France.
Valérie Letscher-BruParasitology and Medical Mycology Laboratory, Strasbourg University Hospital, Strasbourg, France.
Florent MorioNantes Université, CHU Nantes, Cibles et Médicaments des Infections et de l'Immunité, UR1155, Nantes, France.ORCID 0000-0002-5859-6105
Thomas GastinneClinical Hematology Department, Nantes University Hospital, Nantes, France.
Marie-Elisabeth BougnouxMycology and Parasitology Laboratory, Necker-Enfants Malades Hospital, AP-HP, Paris, France.ORCID 0000-0003-4721-2740
Felipe SuarezHematology Department, Necker Enfants Malades Hospital, AP-HP, Paris, France.ORCID 0000-0002-3537-9052
Solène Le GalMycology and Parasitology Department, La Cavale Blanche University Hospital, Brest, France.
Damien DupontMedical Mycology and Parasitology Department, Institut des Agents Infectieux, Hospices Civils de Lyon, Lyon, France.ORCID 0000-0002-6992-1073
Florence AderInfectious Diseases Department, Croix Rousse Hospital, Hospices Civils de Lyon, Lyon, France.
Carine Halfon-DomenechInstitut d'Hématologie et Oncologie Pédiatrique, Hospices Civils de Lyon, Lyon, France.
Sophie Ducastelle-LeprêtreClinical Hematology Department, Hospices Civils de Lyon, Lyon, France.
Françoise BotterelMycology and Parasitology Unit, Henri Mondor University Hospital, AP-HP, Créteil, France.ORCID 0000-0002-3028-2665
Laurence MillonMycology and Parasitology Laboratory, Besançon University Hospital, Besancon, France.ORCID 0000-0001-5939-3409
Gaelle GuillermHematology Department, Morvan Hospital, Brest University Hospital, Brest, France.
Séverine AnsartInfectious Diseases Department, La Cavale Blanche Hospital, Brest University Hospital, Brest, France.
David BoutoilleInfectious Diseases Department, Nantes University Hospital, Nantes, France.
Marie-Pierre LedouxHematology Department, Strasbourg Cancer Institute, Strasbourg, France.
Jean-Etienne HerbrechtIntensive Care Unit, Strasbourg University Hospital, Strasbourg, France.
Christine RobinHematology Department, Henri Mondor Hospital, AP-HP, Créteil, France.
Giovanna MelicaInfectious Diseases Department, Henri Mondor Hospital, AP-HP, Créteil, France.
Dea Garcia-HermosoTranslational Mycology Research Group, Mycology Department, Institut Pasteur, Université Paris Cité, National Reference Center for Invasive Mycoses and Antifungals, Paris, France.
Olivier Lortholary *Infectious Diseases Department, Necker-Enfants Malades Hospital, AP-HP, Paris, France.
Raoul Herbrecht *Hematology Department, Strasbourg Cancer Institute, Strasbourg, France.
Raphaël Porcher *Centre d'Epidémiologie Clinique, Hôtel-Dieu Hospital, AP-HP, Paris, France.
Fanny Lanternier *Infectious Diseases Department, Necker-Enfants Malades Hospital, AP-HP, Paris, France.ORCID 0000-0003-3800-4683

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Management of pulmonary mucormycosis includes intravenous liposomal amphotericin-B (L-AmB), followed by posaconazole or isavuconazole. We aimed to determine the optimal L-AmB duration before switching to triazole therapy. Using data from a retrospective study in France, we performed an emulated trial evaluating stopping L-AmB after 14 days (short treatment) versus continuing L-AmB (long treatment). The benefit of combination L-AmB therapy was also investigated. A cloning, censoring, and weighting approach was used to account for immortal time and indication biases. Ninety-four cases of pulmonary mucormycosis were included, of which 35% had dissemination. Eighty-nine patients received L-AmB first-line therapy for a median of 25 (IQR: 12-54) days, including 18 patients as combination therapy. L-AmB was discontinued for adverse events in 16/89 patients (18%). Treatment was switched to posaconazole (

Indexed as

Amphotericin BAntifungal AgentsLung Diseases, FungalMucormycosisAdultAgedDrug Therapy, CombinationFemaleHumansMaleMiddle AgedNitrilesPyridinesRetrospective StudiesTriazolesAmphotericin BAntifungal Agentsisavuconazoleliposomal amphotericin BNitrilesposaconazolePyridinesTriazolesamphotericin Bemulated trialsisavuconazolemucormycosis

Identifiers

PMID42053464
PMCPMC13231879

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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.