Comedications Associated with Immune-Related Adverse Events from Immune-Checkpoint Inhibitors.

IF 6.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Léonard Laurent, Baptiste Abbar, Kevin Bihan, Elise Dumas, Floriane Jochum, Bénédicte Lebrun-Vignes, Jean-Philippe Spano, Joe-Elie Salem, Anne-Sophie Hamy, Fabien Reyal, Paul Gougis
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Abstract

Immune-checkpoint inhibitors (ICI) have revolutionized cancer treatment but are responsible for various immune-related adverse events (irAE). The impact of non-anticancer medications (comedications) on irAE occurrence remains largely unexplored. The objective of this study was to assess comedications associated with an increased reporting of irAE with ICIs. In this pharmacovigilance study, all individual case safety reports (ICSRs) involving ICIs reported in the World Health Organization international pharmacovigilance database Vigibase up to January 2024 were extracted. All suspect or interacting comedications were analyzed individually and as drug classes using Anatomical Therapeutic Chemical classification level 4. The primary outcome was the reporting odds ratio (ROR) of irAE in patients who received both an ICI and the comedication of interest, compared with ICI-treated patients who did not receive that comedication. Among 169,753 ICSRs involving an ICI, a total of 314,366 comedications were recorded, with 8,122 identified as "suspect or interacting." Analysis shows an increased reporting of nephritis with proton pump inhibitors (PPI) (ROR = 29.62 [95% CI = 18.61-47.14]) and with non-steroidal anti-inflammatory drugs (ROR = 10.47 [95% CI = 4.15-26.41]), myositis with statins (ROR = 9.41 [95% CI = 3.50-25.30]), ketoconazole with hepatitis (ROR = 20.49 [95% CI = 1.53-274.17]) and autoimmune bullous disease with dipeptyl-peptidase-4 inhibitors (ROR = 46.42 [95% CI = 11.71-184.05]), among others. Various drugs, including PPI (ROR = 8.61 [95% CI = 3.48-21.26]), some anti-infectives (sulfamethoxazole, ROR = 31.31 [95% CI = 13.32-73.61], clavulanic acid, ROR = 18.12 [95% CI = 4.77-68.89]), allopurinol (ROR = 57.11 [95% CI = 11.27-289.39]) or levetiracetam (ROR = 14.91 [95% CI = 2.15-103.64]) were associated with serious cutaneous adverse reactions. Complementary analysis showed higher ROR in the ICI population versus without ICI for the association of nephritis with ibuprofen (RORICI = 27.82 vs. RORVigiBaseWithoutICI = 3.56, RORratio = 7.81 [95% CI = 1.23-49.50]) and myocarditis with influenza vaccine (RORICI = 22.74 vs. RORVigiBaseWithoutICI = 0.66, RORratio = 34.45 [95% CI = 1.66-723.24]), suggesting a synergistic toxicity. This study identified multiple comedications associated with an increased reporting of specific irAE. Some of them might be synergistic warranting further investigation.

与免疫检查点抑制剂免疫相关不良事件相关的药物。
免疫检查点抑制剂(ICI)已经彻底改变了癌症治疗,但也导致了各种免疫相关不良事件(irAE)。非抗癌药物(药物)对irAE发生的影响在很大程度上仍未被探索。本研究的目的是评估与ICIs合并irAE报告增加相关的药物。在这项药物警戒研究中,提取了截至2024年1月世界卫生组织国际药物警戒数据库Vigibase中报告的所有涉及ICIs的个案安全报告(ICSRs)。所有可疑或相互作用的药物单独分析,并作为药物类别使用解剖治疗化学分类水平4。主要结局是与未接受ICI治疗的患者相比,同时接受ICI和目标药物治疗的患者发生irAE的报告优势比(ROR)。在涉及ICI的169753份icsr中,共记录了314366种药物,其中8122种被确定为“可疑或相互作用”。分析显示,质子泵抑制剂(PPI)组肾炎(ROR = 29.62 [95% CI = 18.61-47.14])和非甾体抗炎药组肾炎(ROR = 10.47 [95% CI = 4.15-26.41])、他汀类药物组肌炎(ROR = 9.41 [95% CI = 3.50-25.30])、酮康唑组肝炎(ROR = 20.49 [95% CI = 1.53-274.17])和二肽酶-4抑制剂组自身免疫性大疱性疾病(ROR = 46.42 [95% CI = 11.71-184.05])等的报告增加。PPI (ROR = 8.61 [95% CI = 3.48-21.26])、部分抗感染药物(磺胺甲恶唑,ROR = 31.31 [95% CI = 13.32-73.61]、克拉维酸,ROR = 18.12 [95% CI = 4.77-68.89])、别嘌呤醇(ROR = 57.11 [95% CI = 11.27-289.39])或左乙拉西坦(ROR = 14.91 [95% CI = 2.15-103.64])均与严重皮肤不良反应相关。补充分析显示,在布洛芬联合肾炎(RORICI = 27.82 vs. RORVigiBaseWithoutICI = 3.56, ROR比值= 7.81 [95% CI = 1.23-49.50])和心肌炎联合流感疫苗(RORICI = 22.74 vs. RORVigiBaseWithoutICI = 0.66, ROR比值= 34.45 [95% CI = 1.66-723.24])的相关性中,ICI人群的ROR高于非ICI人群,表明两者具有协同毒性。本研究确定了多种药物与特异性irAE报告增加相关。其中一些可能是协同的,值得进一步研究。
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来源期刊
CiteScore
12.70
自引率
7.50%
发文量
290
审稿时长
2 months
期刊介绍: Clinical Pharmacology & Therapeutics (CPT) is the authoritative cross-disciplinary journal in experimental and clinical medicine devoted to publishing advances in the nature, action, efficacy, and evaluation of therapeutics. CPT welcomes original Articles in the emerging areas of translational, predictive and personalized medicine; new therapeutic modalities including gene and cell therapies; pharmacogenomics, proteomics and metabolomics; bioinformation and applied systems biology complementing areas of pharmacokinetics and pharmacodynamics, human investigation and clinical trials, pharmacovigilence, pharmacoepidemiology, pharmacometrics, and population pharmacology.
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