TY - JOUR
T1 - Long-term risk of hepatocellular carcinoma mortality in 23220 hospitalized patients treated with micafungin or other parenteral antifungals
AU - Schneeweiss, Sebastian
AU - Carver, Peggy L.
AU - Datta, Kausik
AU - Galar, Alicia
AU - Johnson, Melissa D.
AU - Letourneau, Alyssa R.
AU - Marty, Francisco M.
AU - Nagel, Jerod
AU - Najdzinowicz, Maryann
AU - Saul, Melissa
AU - Schuster, Mindy
AU - Shoham, Shmuel
AU - Silveira, Fernanda P.
AU - Varughese, Christy
AU - Wilck, Marissa
AU - Weatherby, Lisa
AU - Oene, Joop Van
AU - Walker, Alexander M.
N1 - Funding Information:
S. Schneeweiss is consultant to WHISCON, LLC and to Aetion, Inc., a software manufacturer of which he also owns equity. He is principal investigator of investigator-initiated grants to the Brigham and Women’s Hospital from PCORI, NIH, FDA, Bayer, Vertex and Boehringer Ingelheim unrelated to the topic of this study. A. M. Walker and L. Weatherby are both employees of WHISCON, LLC. M. D. Johnson has received research grants from Charles River Laboratories, Merck & Co. and Scynexis, and is a consultant to Astellas Pharma US. F. M. Marty served as a consultant for WHISCON LLC for the design of the study; he also reports personal fees and non-financial support from Basilea; personal fees and nonfinancial support from Pfizer; grants, personal fees and non-financial support from Merck; personal fees from United Medical; and grants from F2G, outside the submitted work. F. P. Silveira received research support from Pfizer, Shire, Ansun Biopharma, Qiagen and Gilead. S. Shoham is consultant to Theravance, Inc., Biota Pharmaceuticals, Inc. and Cidara Therapeutics, Inc., and received research support from Pfizer, ViroPharma, Inc., Scynexis Inc., Chimerix, Inc., Ansun Biopharma, Inc., Gilead, Merck & Co and Astellas Pharma US, Inc. J. van Oene was an employee of Astellas during the study. M. Wilck reports no conflict of interest while conducting the study. She is now an employee of Merck & Co. All other authors: none to declare
Funding Information:
This study was sponsored by Astellas Pharma Europe BV, Leiden, The Netherlands and by Astellas Pharma Global Development, Inc., Northbrook, IL, USA through a research contract with World Health Information Science Consultants (WHISCON), LLC. Astellas is the manufacturer of micafungin, one of the study drugs. The investigators had full control over protocol development, data collection and analyses, and publication.
Publisher Copyright:
© 2019 The Author(s). Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved.
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Background: Liver tumours observed in rats exposed to micafungin led to a black box warning upon approval in Europe in 2008. Micafungin's risk for liver carcinogenicity in humans has not been investigated. We sought to describe the risk of fatal hepatocellular carcinoma (HCC) among persons who received micafungin and other parenteral antifungals (PAFs) with up to 12 years of follow-up. Methods: We assembled a US multicentre cohort of hospitalized patients who received micafungin or other PAFs between 2005 and 2012. We used propensity score (PS) matching on patient characteristics from electronic medical records to compare rates of HCC mortality identified through the National Death Index though to the end of December 2016. We computed HRs and 95% CIs. Results: A total of 40110 patients who received a PAF were identified; 6903 micafungin recipients (87% of those identified) were successfully matched to 16317 comparator PAF users. Ten incident HCC deaths, one in the micafungin-exposed group and nine among comparator PAF users, occurred in 71285 person-years of follow-up. The HCC mortality rate was 0.05 per 1000 person-years in micafungin patients and 0.17 per 1000 person-years in comparator PAF patients. The PS-matched HR for micafungin versus comparator PAF was 0.29 (95% CI 0.04-2.24). Conclusions: Both micafungin and comparator PAFs were associated with HCC mortality rates of <0.2 per 1000 person-years. Given the very low event rates, any potential risk for HCC should not play a role in clinical decisions regarding treatment with micafungin or other PAFs investigated in this study.
AB - Background: Liver tumours observed in rats exposed to micafungin led to a black box warning upon approval in Europe in 2008. Micafungin's risk for liver carcinogenicity in humans has not been investigated. We sought to describe the risk of fatal hepatocellular carcinoma (HCC) among persons who received micafungin and other parenteral antifungals (PAFs) with up to 12 years of follow-up. Methods: We assembled a US multicentre cohort of hospitalized patients who received micafungin or other PAFs between 2005 and 2012. We used propensity score (PS) matching on patient characteristics from electronic medical records to compare rates of HCC mortality identified through the National Death Index though to the end of December 2016. We computed HRs and 95% CIs. Results: A total of 40110 patients who received a PAF were identified; 6903 micafungin recipients (87% of those identified) were successfully matched to 16317 comparator PAF users. Ten incident HCC deaths, one in the micafungin-exposed group and nine among comparator PAF users, occurred in 71285 person-years of follow-up. The HCC mortality rate was 0.05 per 1000 person-years in micafungin patients and 0.17 per 1000 person-years in comparator PAF patients. The PS-matched HR for micafungin versus comparator PAF was 0.29 (95% CI 0.04-2.24). Conclusions: Both micafungin and comparator PAFs were associated with HCC mortality rates of <0.2 per 1000 person-years. Given the very low event rates, any potential risk for HCC should not play a role in clinical decisions regarding treatment with micafungin or other PAFs investigated in this study.
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U2 - 10.1093/jac/dkz396
DO - 10.1093/jac/dkz396
M3 - Article
C2 - 31580432
AN - SCOPUS:85076446403
SN - 0305-7453
VL - 75
SP - 221
EP - 228
JO - Journal of Antimicrobial Chemotherapy
JF - Journal of Antimicrobial Chemotherapy
IS - 1
ER -