Novel evidence for the prognostic impact of β-blockers in solid cancer patients receiving immune checkpoint inhibitors

医学 危险系数 内科学 子群分析 荟萃分析 肿瘤科 肺癌 癌症 回顾性队列研究 科克伦图书馆 置信区间 临床试验
作者
Xuebing Yan,Peipei Liu,Donglin Li,Ru Hu,Mingyang Tao,Siyuan Zhu,Wenjuan Wu,Mengxue Yang,Xiao Qu
出处
期刊:International Immunopharmacology [Elsevier BV]
卷期号:113 (Pt A): 109383-109383 被引量:23
标识
DOI:10.1016/j.intimp.2022.109383
摘要

Cancer immunotherapy based on immune checkpoint inhibitors (ICIs) has made encouraging achievements in both clinical trials and real-world studies. The β-blockers, as common concomitant medications in clinical practice, have been suggested to exert anti-cancer effects in various human malignancies. This study aimed to clarify the prognostic impact of β-blockers in solid cancer patients receiving ICI therapy.A systematic literature review and meta-analysis was firstly performed based on databases including PubMed, Cochrane Library, Web of Science, Embase, and Clinicaltrials.gov before August 1th 2022. The association of β-blocker use with overall survival (OS) or progression-free survival (PFS) was determined using the hazard ratios (HRs) coupled with 95% confidence intervals (CIs). Then, a retrospective study enrolling 194 patients was performed to validate the results of the meta-analysis.A total of 11 studies enrolling 10,156 patients were included in the meta-analysis. The pooled analysis demonstrated β-blocker use was not significantly correlated with either OS (HR = 0.97(0.85-1.11)) or PFS (HR = 0.98(0.90-1.06)). Similar results were also observed in the subgroup analysis stratified by cancer type, age, sample size and ICI therapy, except for the OS (HR = 0.61(0.45-0.83)) and PFS (HR = 0.65(0.44-0.96)) in the studies with sample size less than 200. The retrospective study indicated no significant correlation between β-blocker use and the clinical outcome in the entire cohort and lung cancer subgroup. However, β-blocker use was found to be significantly associated with better objective response to ICI-based therapy in the entire cohort (odds ratio (OR) = 0.42(0.19-0.94), p = 0.036) and lung cancer subgroup (OR = 0.25(0.08-0.83), p = 0.024).Although both our up-to-date meta-analysis and retrospective study suggested β-blocker use has no significant impact on the overall prognosis of solid cancer patients receiving ICIs, β-blocker use may be associated with improved anti-cancer efficacy of ICIs. Considering study limitations, more clinical validations and mechanism investigations are of great necessity for clarifying the role of β-blockers in ICI-based therapy.
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