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Micafungin prophylaxis for acute leukemia patients undergoing induction chemotherapy

BACKGROUND: Micafungin is a well-tolerated and effective prophylactic antifungal agent used in hematologic diseases. In this prospective trial, we evaluated the efficacy and safety of prophylactic micafungin during first induction chemotherapy in patients with acute leukemia. We also compared outcom...

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Autores principales: Park, Hyunkyung, Youk, Jeonghwan, Shin, Dong-Yeop, Hong, Junshik, Kim, Inho, Kim, Nam Joong, Lee, Jeong-Ok, Bang, Soo-Mee, Yoon, Sung-Soo, Park, Wan Beom, Koh, Youngil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469030/
https://www.ncbi.nlm.nih.gov/pubmed/30991992
http://dx.doi.org/10.1186/s12885-019-5557-9
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author Park, Hyunkyung
Youk, Jeonghwan
Shin, Dong-Yeop
Hong, Junshik
Kim, Inho
Kim, Nam Joong
Lee, Jeong-Ok
Bang, Soo-Mee
Yoon, Sung-Soo
Park, Wan Beom
Koh, Youngil
author_facet Park, Hyunkyung
Youk, Jeonghwan
Shin, Dong-Yeop
Hong, Junshik
Kim, Inho
Kim, Nam Joong
Lee, Jeong-Ok
Bang, Soo-Mee
Yoon, Sung-Soo
Park, Wan Beom
Koh, Youngil
author_sort Park, Hyunkyung
collection PubMed
description BACKGROUND: Micafungin is a well-tolerated and effective prophylactic antifungal agent used in hematologic diseases. In this prospective trial, we evaluated the efficacy and safety of prophylactic micafungin during first induction chemotherapy in patients with acute leukemia. We also compared outcomes of prophylactic micafungin with those of prophylactic posaconazole in acute myeloid leukemia (AML). METHODS: Medically fit patients with newly diagnosed acute leukemia received 50 mg micafungin intravenously once daily from the initiation of first induction chemotherapy to recovery of neutrophil count, suspected fungal infection, or unacceptable drug-related toxicity (Clinicaltrials.gov number, NCT02440178). The primary end point was incidence of invasive fungal infection, and the secondary end points were adverse events of prophylactic micafungin and mortality during induction therapy. RESULTS: The 65 patients (median age = 51 years, male:female = 34:31) enrolled in this study had diagnoses of AML (33, 50.8%), acute lymphoblastic leukemia (31, 47.7%), and acute biphenotypic leukemia (1, 1.5%). Median duration of micafungin treatment was 24 days (range 1–68), with proven invasive fungal disease in one patient (1.5%) and possible fungal infection in two patients (3.1%). Three of the patients (4.6%) experienced the following adverse events, but all events were tolerable: liver function abnormality (Grade 2, n = 1; Grade 3, n = 1) and allergic reaction (Grade 2, n = 1). Three patients died during induction therapy, and invasive aspergillosis pneumonia was the cause of death for one of those patients. Overall, 19 patients (29.2%) discontinued prophylactic micafungin, and 18 (27.7%) patients switched to another antifungal agent. We observed no fungal infections caused by amphotericin B-resistant organisms. In AML patients, outcomes of prophylactic micafungin during induction chemotherapy did not differ significantly with those of prophylactic posaconazole with regard to incidence of fungal infections, rate of discontinuation, or safety. CONCLUSIONS: Our study demonstrates that prophylactic micafungin is safe and effective in patients with acute leukemia undergoing induction chemotherapy. Outcomes in patients with AML were similar to those of prophylactic posaconazole, indicating the usefulness of micafungin as a prophylactic antifungal agent during induction chemotherapy for AML. TRIAL REGISTRATION: Clinicaltrials.gov NCT02440178, registered May 12th 2015.
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spelling pubmed-64690302019-04-23 Micafungin prophylaxis for acute leukemia patients undergoing induction chemotherapy Park, Hyunkyung Youk, Jeonghwan Shin, Dong-Yeop Hong, Junshik Kim, Inho Kim, Nam Joong Lee, Jeong-Ok Bang, Soo-Mee Yoon, Sung-Soo Park, Wan Beom Koh, Youngil BMC Cancer Research Article BACKGROUND: Micafungin is a well-tolerated and effective prophylactic antifungal agent used in hematologic diseases. In this prospective trial, we evaluated the efficacy and safety of prophylactic micafungin during first induction chemotherapy in patients with acute leukemia. We also compared outcomes of prophylactic micafungin with those of prophylactic posaconazole in acute myeloid leukemia (AML). METHODS: Medically fit patients with newly diagnosed acute leukemia received 50 mg micafungin intravenously once daily from the initiation of first induction chemotherapy to recovery of neutrophil count, suspected fungal infection, or unacceptable drug-related toxicity (Clinicaltrials.gov number, NCT02440178). The primary end point was incidence of invasive fungal infection, and the secondary end points were adverse events of prophylactic micafungin and mortality during induction therapy. RESULTS: The 65 patients (median age = 51 years, male:female = 34:31) enrolled in this study had diagnoses of AML (33, 50.8%), acute lymphoblastic leukemia (31, 47.7%), and acute biphenotypic leukemia (1, 1.5%). Median duration of micafungin treatment was 24 days (range 1–68), with proven invasive fungal disease in one patient (1.5%) and possible fungal infection in two patients (3.1%). Three of the patients (4.6%) experienced the following adverse events, but all events were tolerable: liver function abnormality (Grade 2, n = 1; Grade 3, n = 1) and allergic reaction (Grade 2, n = 1). Three patients died during induction therapy, and invasive aspergillosis pneumonia was the cause of death for one of those patients. Overall, 19 patients (29.2%) discontinued prophylactic micafungin, and 18 (27.7%) patients switched to another antifungal agent. We observed no fungal infections caused by amphotericin B-resistant organisms. In AML patients, outcomes of prophylactic micafungin during induction chemotherapy did not differ significantly with those of prophylactic posaconazole with regard to incidence of fungal infections, rate of discontinuation, or safety. CONCLUSIONS: Our study demonstrates that prophylactic micafungin is safe and effective in patients with acute leukemia undergoing induction chemotherapy. Outcomes in patients with AML were similar to those of prophylactic posaconazole, indicating the usefulness of micafungin as a prophylactic antifungal agent during induction chemotherapy for AML. TRIAL REGISTRATION: Clinicaltrials.gov NCT02440178, registered May 12th 2015. BioMed Central 2019-04-16 /pmc/articles/PMC6469030/ /pubmed/30991992 http://dx.doi.org/10.1186/s12885-019-5557-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Park, Hyunkyung
Youk, Jeonghwan
Shin, Dong-Yeop
Hong, Junshik
Kim, Inho
Kim, Nam Joong
Lee, Jeong-Ok
Bang, Soo-Mee
Yoon, Sung-Soo
Park, Wan Beom
Koh, Youngil
Micafungin prophylaxis for acute leukemia patients undergoing induction chemotherapy
title Micafungin prophylaxis for acute leukemia patients undergoing induction chemotherapy
title_full Micafungin prophylaxis for acute leukemia patients undergoing induction chemotherapy
title_fullStr Micafungin prophylaxis for acute leukemia patients undergoing induction chemotherapy
title_full_unstemmed Micafungin prophylaxis for acute leukemia patients undergoing induction chemotherapy
title_short Micafungin prophylaxis for acute leukemia patients undergoing induction chemotherapy
title_sort micafungin prophylaxis for acute leukemia patients undergoing induction chemotherapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469030/
https://www.ncbi.nlm.nih.gov/pubmed/30991992
http://dx.doi.org/10.1186/s12885-019-5557-9
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