Evidence map›Paper›PMID 41718446›Full record

ArticleMycoses2026

Rezafungin for Salvage or Consolidation Therapy of Invasive Fungal Disease: Experience in Real-World Clinical Practice.

Jorge Boán, Eduardo Aparicio-Minguijón, Mario Fernández-Ruiz, María Asunción Pérez-Jacoiste Asín, Isabel Rodríguez-Goncer, Francisco López-Medrano, Rafael San-Juan, José Tiago Silva, Ana Pérez-Ayala, Jose Manuel Caro-Teller and 1 more

Abstract read
In one paragraph

Article in Mycoses, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Trial
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

11 authors.

Jorge BoánUnit of Infectious Diseases, Hospital Universitario 12 de Octubre, Instituto de Investigación Hospital 12 de Octubre (imas12), Madrid, Spain.ORCID https://orcid.org/0000-0003-2682-0819
Eduardo Aparicio-MinguijónUnit of Infectious Diseases, Hospital Universitario 12 de Octubre, Instituto de Investigación Hospital 12 de Octubre (imas12), Madrid, Spain.ORCID https://orcid.org/0009-0007-1497-8770
Mario Fernández-RuizUnit of Infectious Diseases, Hospital Universitario 12 de Octubre, Instituto de Investigación Hospital 12 de Octubre (imas12), Madrid, Spain.ORCID https://orcid.org/0000-0002-0315-8001
María Asunción Pérez-Jacoiste AsínUnit of Infectious Diseases, Hospital Universitario 12 de Octubre, Instituto de Investigación Hospital 12 de Octubre (imas12), Madrid, Spain.ORCID https://orcid.org/0000-0002-0477-2337
Isabel Rodríguez-GoncerUnit of Infectious Diseases, Hospital Universitario 12 de Octubre, Instituto de Investigación Hospital 12 de Octubre (imas12), Madrid, Spain.ORCID https://orcid.org/0000-0003-2150-5748
Francisco López-MedranoUnit of Infectious Diseases, Hospital Universitario 12 de Octubre, Instituto de Investigación Hospital 12 de Octubre (imas12), Madrid, Spain.ORCID https://orcid.org/0000-0001-5333-7529
Rafael San-JuanUnit of Infectious Diseases, Hospital Universitario 12 de Octubre, Instituto de Investigación Hospital 12 de Octubre (imas12), Madrid, Spain.ORCID https://orcid.org/0000-0003-3446-1991
José Tiago SilvaUnit of Infectious Diseases, Hospital Universitario 12 de Octubre, Instituto de Investigación Hospital 12 de Octubre (imas12), Madrid, Spain.ORCID https://orcid.org/0000-0001-8765-3466
Ana Pérez-AyalaSchool of Medicine, Universidad Complutense, Madrid, Spain.ORCID https://orcid.org/0000-0001-6426-6279
Jose Manuel Caro-TellerDepartment of Pharmacy, Hospital Universitario 12 de Octubre, Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Madrid, Spain.ORCID https://orcid.org/0000-0002-3043-653X
José María AguadoUnit of Infectious Diseases, Hospital Universitario 12 de Octubre, Instituto de Investigación Hospital 12 de Octubre (imas12), Madrid, Spain.ORCID https://orcid.org/0000-0002-9520-8255

Funding

Instituto de Salud Carlos III (ISCIII), Spanish Ministry of Science, Innovation and Universities. CM25/00243Instituto de Salud Carlos III (ISCIII), Spanish Ministry of Science, Innovation and Universities. CM25/00250Instituto de Salud Carlos III (ISCIII), Spanish Ministry of Science, Innovation and Universities. JR24/00034
6 · The paper itself

Abstract

backgroundEchinocandins are the first-line treatment for invasive candidiasis. Rezafungin is a novel echinocandin with improved pharmacokinetic properties that allow for once-weekly intravenous administration, offering potential advantages in complex clinical settings.

objectivesWe aimed to describe our real-world experience with rezafungin for the treatment of invasive fungal disease (IFD). PATIENTS: A retrospective analysis of consecutive patients treated with rezafungin for proven IFD at our center between September 2022 and December 2025 was conducted.

resultsWe included 13 patients (mean age: 59.4 ± 17.8 years). Main predisposing conditions included immunosuppression (53.8% [solid organ transplantation in 30.8%]), solid cancer (30.8%) and recent surgical intervention (38.5%). Most frequent Candida species were C. albicans (38.5%), C. parapsilosis (30.8%) and Nakaseomyces glabratus (15.4%). One patient had necrotizing gingival infection due to Trichoderma longibrachiatum. Main types of IFD included intravascular Candida infection (38.5%) and surgical-site and intra-abdominal candidiasis (23.1% each). Reported reasons for initiating rezafungin were the presence of fluconazole-resistant isolates (53.8%), facilitating outpatient antifungal therapy (30.8%) and avoiding anticipated drug-drug interactions with triazoles (15.4%). No patient received rezafungin as a first-line treatment and most (92.3%) had been previously exposed to other echinocandins. Rezafungin was typically initiated upon clearance of follow-up blood cultures (80.0%). Median number of weekly doses was 4.0 (interquartile range: 3.0-5.5). Clinical cure (complete or partial response) by day +30 was achieved in all evaluable patients (100.0% [12/12]), with no treatment-emergent adverse events.

conclusionsRezafungin was effective and safe as salvage or consolidation therapy in patients with IFD, including deep-seated candidiasis.

Indexed as

Antifungal AgentsEchinocandinsInvasive Fungal InfectionsSalvage TherapyAdultAgedBreakthrough InfectionsCandidaCandidiasis, InvasiveFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeAntifungal AgentsEchinocandinsRezafungincandidemiainvasive candidiasisreal‐world experiencerezafungin

Identifiers

PMID41718446
PMCPMC12922572

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.