Matched-paired analysis of patients treated for invasive mucormycosis: standard treatment versus posaconazole new formulations (MoveOn)
Language English Country Great Britain, England Media print
Document type Clinical Trial, Journal Article, Observational Study, Research Support, Non-U.S. Gov't
PubMed
31393591
DOI
10.1093/jac/dkz344
PII: 5545108
Knihovny.cz E-resources
- MeSH
- Amphotericin B therapeutic use MeSH
- Matched-Pair Analysis MeSH
- Antifungal Agents administration & dosage chemistry MeSH
- Child MeSH
- Adult MeSH
- Invasive Fungal Infections drug therapy MeSH
- Infant MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Mucorales drug effects MeSH
- Mucormycosis blood drug therapy MeSH
- Infant, Newborn MeSH
- Child, Preschool MeSH
- Drug Compounding MeSH
- Prospective Studies MeSH
- Registries MeSH
- Aged MeSH
- Triazoles administration & dosage chemistry MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Infant MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Infant, Newborn MeSH
- Child, Preschool MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Observational Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Amphotericin B MeSH
- Antifungal Agents MeSH
- liposomal amphotericin B MeSH Browser
- posaconazole MeSH Browser
- Triazoles MeSH
BACKGROUND: First-line antifungal treatment for invasive mucormycosis (IM) consists of liposomal amphotericin B. Salvage treatment options are limited and often based on posaconazole oral suspension. With the approval of posaconazole new formulations, patients could benefit from improved pharmacokinetics, safety and tolerability. OBJECTIVES: Our aim was to assess the effectiveness of posaconazole new formulations for IM treatment. METHODS: We performed a case-matched analysis with proven or probable IM patients from the FungiScope® Registry. First-line posaconazole new formulations (1st-POSnew) and first-line amphotericin B plus posaconazole new formulations (1st-AMB+POSnew) cases were matched with first-line amphotericin B-based (1st-AMB) treatment controls. Salvage posaconazole new formulations (SAL-POSnew) cases were matched with salvage posaconazole oral suspension (SAL-POSsusp) controls. Each case was matched with up to three controls (based on severity, haematological/oncological malignancy, surgery and/or renal dysfunction). RESULTS: Five patients receiving 1st-POSnew, 18 receiving 1st-AMB+POSnew and 22 receiving SAL-POSnew were identified. By day 42, a favourable response was reported for 80.0% (n = 4/5) of patients receiving 1st-POSnew, for 27.8% (n = 5/18) receiving 1st-AMB+POSnew and for 50.0% (n = 11/22) receiving SAL-POSnew. Day 42 all-cause mortality of patients receiving posaconazole new formulations was lower compared with controls [20.0% (n = 1/5) in 1st-POSnew versus 53.3% (n = 8/15) in 1st-AMB; 33.3% (n = 6/18) in 1st-AMB+POSnew versus 52.0% (n = 26/50) in 1st-AMB; and 0.0% (n = 0/22) in SAL-POSnew versus 4.4% (n = 2/45) in SAL-POSsusp]. CONCLUSIONS: Posaconazole new formulations were effective in terms of treatment response and associated mortality of IM. While posaconazole new formulations may be an alternative for treatment of IM, the limited sample size of our study calls for a cautious interpretation of these observations.
Center for Integrated Oncology CIO Köln Bonn Medical Faculty University of Cologne Cologne Germany
Center for Molecular Medicine Cologne University of Cologne Cologne Germany
Clinical Microbiology and Parasitology Department University Hospital La Paz Madrid Spain
Clinical Trials Centre Cologne University of Cologne Cologne Germany
Department of Infectious Diseases Royal Perth Hospital Perth WA Australia
Department of Internal Medicine 2 Julius Maximilians University Würzburg Germany
Department of Internal Medicine 3 University of Munich Munich Germany
Department of Internal Medicine Hematology and Oncology Masaryk University Brno Czech Republic
Department of Medicine San Diego Veterans Affairs Medical Center San Diego CA USA
Division of Infectious Diseases University of California San Diego San Diego CA USA
German Centre for Infection Research partner site Bonn Cologne Cologne Germany
Inserm U1100 Tours University Tours France
Institute for Virology and Clinical Microbiology Witten Herdecke University Witten Germany
Parasitology Mycology and Tropical Medicine Service University Hospital of Tours Tours France
School of Pathology and Laboratory Medicine University of Western Australia Perth WA Australia
University Hospital Brno Brno Czech Republic
University of Cologne Institute for Medical Microbiology Immunology and Hygiene Cologne Germany
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