Efficacy of Biologics in Patients with Allergic Bronchopulmonary Aspergillosis: A Systematic Review and Meta-Analysis

被引:7
作者
Chen, Xiaoying [1 ]
Zhi, Haopeng [1 ]
Wang, Xiaohu [2 ]
Zhou, Zicong [1 ]
Luo, Huiting [1 ]
Li, Jing [1 ]
Sehmi, Roma [3 ,4 ]
O'Byrne, Paul M. [3 ,4 ]
Chen, Ruchong [1 ,5 ]
机构
[1] Guangzhou Med Univ, Natl Ctr Resp Med, State Key Lab Resp Dis,Natl Clin Res Ctr Resp Dis,, Dept Allergy & Clin Immunol,Guangzhou Inst Resp Hl, Guangzhou, Guangdong, Peoples R China
[2] Peoples Hosp Yangjiang, Dept Resp & Crit Care Med, Yangjiang, Guangdong, Peoples R China
[3] St Josephs Healthcare, Firestone Inst Resp Hlth, Dept Med, Hamilton, ON, Canada
[4] McMaster Univ, Hamilton, ON, Canada
[5] Guangzhou Natl Lab, Guangzhou, Peoples R China
关键词
Allergic Bronchopulmonary Aspergillosis; ABPA; Biological agents; Efficacy; meta-analysis; INDIVIDUAL PARTICIPANT DATA; ANTI-IGE ANTIBODY; OMALIZUMAB TREATMENT; CYSTIC-FIBROSIS; SEVERE ASTHMA; IMMUNOGLOBULIN-E; THERAPY; MEPOLIZUMAB; BENRALIZUMAB; ABPA;
D O I
10.1007/s00408-024-00717-y
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background Treatment of allergic bronchopulmonary aspergillosis (ABPA) is challenging. Biological therapies have been reported as adjunctive treatments for ABPA, primarily in case series or case reports. This study aimed to analyze the efficacy of biologics for managing ABPA both qualitatively and quantitatively. Methods All articles on APBA published in October 2023 were searched in PubMed, Web of Science, ClinicalTrials.gov, and Embase databases. The effects of interest were the mean changes from baseline for outcomes, including exacerbation rates, oral corticosteroids usage (OCS), and total immunoglobulin E (IgE) levels. Reported outcomes were quantitatively synthesized by usual or individual patient data (IPD) meta-analyses. PROSPERO registration number: CRD42022373396. Results A total of 86 studies were included in the systematic review including 346 patients. Sixteen studies on omalizumab were pooled for the usual meta-analysis. Omalizumab therapy significantly reduced exacerbation rates (- 2.29 [95%CI - 3.32, - 1.26]), OCS dosage (- 10.91 mg [95%CI - 18.98, - 2.85]), and total IgE levels (- 273.07 IU/mL [95%CI - 379.30, - 166.84]), meanwhile improving FEV1% predicted (10.09% [95%CI 6.62, 13.55]). Thirty-one studies on dupilumab, mepolizumab, or benralizumab were pooled to perform an IPD meta-analysis, retrospectively. Both dupilumab and mepolizumab significantly reduced exacerbation rates, OCS, and total IgE levels. Benralizumab showed a similar trend, but it was not statistically significant. Tezepelumab showed weak evidence of its effects on ABPA. All five biologics led to milder clinical symptoms (e.g., cough, wheezing) with serious adverse effects that happened once in omalizumab treatment. Conclusion These results indicate the clinical benefit of omalizumab, dupilumab, and mepolizumab in patients with ABPA. Further randomized, controlled studies with a larger sample size and longer follow-up are needed to confirm these findings.
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页码:367 / 383
页数:17
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