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Micafungin prophylaxis for acute leukemia patients undergoing induction chemotherapy

DC Field Value Language
dc.contributor.authorPark, Hyunkyung-
dc.contributor.authorYouk, Jeonghwan-
dc.contributor.authorShin, Dong-Yeop-
dc.contributor.authorHong, Junshik-
dc.contributor.authorKim, Inho-
dc.contributor.authorKim, Nam Joong-
dc.contributor.authorLee, Jeong-Ok-
dc.contributor.authorBang, Soo-Mee-
dc.contributor.authorYoon, Sung-Soo-
dc.contributor.authorPark, Wan Beom-
dc.contributor.authorKoh, Youngil-
dc.date.accessioned2019-05-13T02:08:57Z-
dc.date.available2019-05-13T11:09:54Z-
dc.date.issued2019-04-16-
dc.identifier.citationBMC Cancer, 19(1):358ko_KR
dc.identifier.issn1471-2407-
dc.identifier.urihttps://hdl.handle.net/10371/153244-
dc.description.abstractBackground
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.
ko_KR
dc.description.sponsorshipThis study was funded by Astellas Pharma Korea, Inc. Funding source had no role in the study design, data collection, data analysis or data interpretation.ko_KR
dc.language.isoenko_KR
dc.publisherBioMed Centralko_KR
dc.subjectAcute leukemiako_KR
dc.subjectProphylaxisko_KR
dc.subjectAntifungal agentko_KR
dc.subjectMicafunginko_KR
dc.subjectPosaconazoleko_KR
dc.titleMicafungin prophylaxis for acute leukemia patients undergoing induction chemotherapyko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor박현경-
dc.contributor.AlternativeAuthor윤정환-
dc.contributor.AlternativeAuthor신동엽-
dc.contributor.AlternativeAuthor홍준식-
dc.contributor.AlternativeAuthor김인호-
dc.contributor.AlternativeAuthor김남중-
dc.contributor.AlternativeAuthor이정옥-
dc.contributor.AlternativeAuthor장수미-
dc.contributor.AlternativeAuthor윤성수-
dc.contributor.AlternativeAuthor박완범-
dc.contributor.AlternativeAuthor고영길-
dc.identifier.doi10.1186/s12885-019-5557-9-
dc.language.rfc3066en-
dc.rights.holderThe Author(s).-
dc.date.updated2019-04-21T03:18:29Z-
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