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Successful treatment of Trichosporon asahii fungemia with isavuconazole in a patient with hematologic malignancies
Trichosporon spp. are yeast-like microorganisms responsible for skin, urinary, pulmonary, or bloodstream infections. Due to intrinsic resistance to echinocandins, poor susceptibility to polyenes, and preferred occurrence in immunocompromised patients, such infections are often of poor prognosis. Yet...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628197/ https://www.ncbi.nlm.nih.gov/pubmed/31372009 http://dx.doi.org/10.2147/IDR.S211148 |
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author | Feugray, Guillaume Krzisch, Daphné Dehais, Marion Razakandrainibe, Romy Gargala, Gilles Favennec, Loic Lepretre, Stéphane Camus, Vincent Costa, Damien |
author_facet | Feugray, Guillaume Krzisch, Daphné Dehais, Marion Razakandrainibe, Romy Gargala, Gilles Favennec, Loic Lepretre, Stéphane Camus, Vincent Costa, Damien |
author_sort | Feugray, Guillaume |
collection | PubMed |
description | Trichosporon spp. are yeast-like microorganisms responsible for skin, urinary, pulmonary, or bloodstream infections. Due to intrinsic resistance to echinocandins, poor susceptibility to polyenes, and preferred occurrence in immunocompromised patients, such infections are often of poor prognosis. Yet no consensual therapeutic guidelines are presently available. Several clinical cases of Trichosporon infections have been successfully treated with azole therapy, including voriconazole which appeared frequently effective against Trichosporon both in vitro and in vivo. However, the low efficacy associated with some Trichosporon genotypes, complex pharmacokinetics, and the side effects of voriconazole represent limitations for its use and has prompted a search for other therapeutic options. Here, we report a case of T. asahii fungemia in a patient with B-cell acute lymphoblastic leukemia which was successfully treated with isavuconazole consecutive to stopping voriconazole therapy due to severe side effects. This observation suggests that isavuconazole with a similar spectrum to voriconazole, fewer pharmacology interactions, and side effects may be considered as a valuable therapeutic option against Trichosporon infections. |
format | Online Article Text |
id | pubmed-6628197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-66281972019-08-01 Successful treatment of Trichosporon asahii fungemia with isavuconazole in a patient with hematologic malignancies Feugray, Guillaume Krzisch, Daphné Dehais, Marion Razakandrainibe, Romy Gargala, Gilles Favennec, Loic Lepretre, Stéphane Camus, Vincent Costa, Damien Infect Drug Resist Case Report Trichosporon spp. are yeast-like microorganisms responsible for skin, urinary, pulmonary, or bloodstream infections. Due to intrinsic resistance to echinocandins, poor susceptibility to polyenes, and preferred occurrence in immunocompromised patients, such infections are often of poor prognosis. Yet no consensual therapeutic guidelines are presently available. Several clinical cases of Trichosporon infections have been successfully treated with azole therapy, including voriconazole which appeared frequently effective against Trichosporon both in vitro and in vivo. However, the low efficacy associated with some Trichosporon genotypes, complex pharmacokinetics, and the side effects of voriconazole represent limitations for its use and has prompted a search for other therapeutic options. Here, we report a case of T. asahii fungemia in a patient with B-cell acute lymphoblastic leukemia which was successfully treated with isavuconazole consecutive to stopping voriconazole therapy due to severe side effects. This observation suggests that isavuconazole with a similar spectrum to voriconazole, fewer pharmacology interactions, and side effects may be considered as a valuable therapeutic option against Trichosporon infections. Dove 2019-07-09 /pmc/articles/PMC6628197/ /pubmed/31372009 http://dx.doi.org/10.2147/IDR.S211148 Text en © 2019 Feugray et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Case Report Feugray, Guillaume Krzisch, Daphné Dehais, Marion Razakandrainibe, Romy Gargala, Gilles Favennec, Loic Lepretre, Stéphane Camus, Vincent Costa, Damien Successful treatment of Trichosporon asahii fungemia with isavuconazole in a patient with hematologic malignancies |
title | Successful treatment of Trichosporon asahii fungemia with isavuconazole in a patient with hematologic malignancies |
title_full | Successful treatment of Trichosporon asahii fungemia with isavuconazole in a patient with hematologic malignancies |
title_fullStr | Successful treatment of Trichosporon asahii fungemia with isavuconazole in a patient with hematologic malignancies |
title_full_unstemmed | Successful treatment of Trichosporon asahii fungemia with isavuconazole in a patient with hematologic malignancies |
title_short | Successful treatment of Trichosporon asahii fungemia with isavuconazole in a patient with hematologic malignancies |
title_sort | successful treatment of trichosporon asahii fungemia with isavuconazole in a patient with hematologic malignancies |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628197/ https://www.ncbi.nlm.nih.gov/pubmed/31372009 http://dx.doi.org/10.2147/IDR.S211148 |
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