Mortality in chronic pulmonary aspergillosis: a systematic review and individual patient data meta-analysis
- PMID: 39617023
- DOI: 10.1016/S1473-3099(24)00567-X
Mortality in chronic pulmonary aspergillosis: a systematic review and individual patient data meta-analysis
Erratum in
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Correction to Lancet Infect Dis 2025; 25: 312-24.Lancet Infect Dis. 2025 Mar;25(3):e137. doi: 10.1016/S1473-3099(25)00098-2. Lancet Infect Dis. 2025. PMID: 40021338 No abstract available.
Abstract
Background: Despite antifungal treatment, chronic pulmonary aspergillosis (CPA) is associated with substantial morbidity and mortality. We conducted a systematic review and meta-analysis to evaluate rates of mortality and its predictors in CPA.
Methods: A systematic literature search was conducted across MEDLINE (PubMed), Scopus, Embase, and Web of Science to identify studies in English, reporting mortality in CPA, from database inception to Aug 15, 2023. We included clinical studies, observational studies, controlled trials, and abstracts. Case reports, animal studies, letters, news, and literature reviews were excluded. Authors of studies published since 2016 were also contacted to obtain anonymised individual patient data (IPD); for other studies, summary estimates were extracted. Subgroup analysis was done for differences in overall 1-year and 5-year mortality, data source, study design, risk of bias, country, Human Development Index, age groups, and the underlying lung disease. We used random-effects meta-analyses to estimate pooled mortality rates. Subgroup analyses and meta-regression were done to explore sources of heterogeneity. One-stage meta-analysis with a stratified Cox proportional hazards model was used to estimate the univariable and hazards for mortality, adjusting for age, sex, type of CPA, treatment, and underlying pulmonary comorbidities. This study was registered with PROSPERO (CRD42023453447).
Findings: We included 79 studies involving 8778 patients in the overall pooled analysis and 15 studies involving 1859 patients in the IPD meta-analysis. Pooled mortality (from 70 studies) was estimated at 27% overall (95% CI 22-32; I2 =95·4%), 15% at 1 year (11-19; I2 =91·6%), and 32% at 5 years (25-39; I2 =94·3%). Overall mortality in patients with CPA with pulmonary tuberculosis as the predominant predisposing condition was 25% (16-35; I2 =87·5%; 20 studies) and with chronic obstructive pulmonary disease was 35% (22-49; I2 =89·7%; 14 studies). Mortality in cohorts of patients who underwent surgical resection was low at 3% (2-4). In the multivariable analysis, among predisposing respiratory conditions, pulmonary tuberculosis history had the lowest mortality hazard (relative to an absence of the disease at baseline), whereas worse outcomes were seen with underlying malignancy; subacute invasive pulmonary aspergillosis and chronic cavitary pulmonary aspergillosis subtypes of CPA were also significantly associated with increased mortality relative to simple aspergilloma on multivariable analysis. Mortality hazard increased by 25% with each decade of age (adjusted hazard ratio 1·25 [95% CI 1·14-1·36], p<0·0001).
Interpretation: CPA is associated with substantial mortality. Advancing age, CPA subtype, and underlying comorbidities are important predictors of mortality. Future studies should focus on identifying appropriate treatment strategies tailored to different risk groups.
Funding: None.
Copyright © 2025 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.
Conflict of interest statement
Declaration of interests AR has received a grant from Jolly Healthcare. KI has received payments from Pfizer Japan. MT has received grants from the Japan Society for the Promotion of Science and The Rotary Foundation; consulting fees from Asahi Kasei Pharma; and honoraria from Sumitomo Pharma, Kyorin Holdings, Astellas Pharma, Ono Pharmaceutical, Fujifilm Toyama Chemical, Chugai Pharmaceutical, Asahi Kasei Pharma, Janssen Pharmaceutical, and Shionogi Healthcare. TT has received consulting fees or honoraria for speaking from Asahikasei, Insmed, and Shionogi. DWD and family hold founder shares in F2G, a University of Manchester spin-out antifungal discovery company; and hold share options in TFF Pharmaceuticals. DWD acts or has recently acted as a consultant to Pulmocide, Biosergen, TFF Pharmaceuticals, Rostra Therapeutics, Pfizer, Mundipharma, Lifemine, and Cipla; chairs a data review committee for Pulmocide and Biosergen; has (in the past 3 years) been paid for talks on behalf of Hikma, Gilead, Avni, Pfizer, and Knight; and has contributed to multiple guidelines related to aspergillosis and fungal diagnostics. All other authors declare no competing interests.
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