Department of Pharmacy Practice, National Institute of Pharmaceutical Education and Research (NIPER), SAS Nagar (Mohali), Punjab, India.
Leukemia/BMT Program of British Columbia, Division of Hematology, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
Ann Hematol. 2024 Aug;103(8):3179-3191. doi: 10.1007/s00277-024-05676-1. Epub 2024 Feb 26.
Concerns persist about venetoclax's long-term safety in larger populations, with limited evidence of infrequent and delayed adverse events (AEs). The study integrated safety data on venetoclax in leukemia patients from randomized controlled trials (RCTs) and FDA adverse event monitoring system (FAERS). We systematically reviewed RCTs reporting safety outcomes of venetoclax in adult leukemia patients of any gender, either monotherapy or in combination, applying advanced search on databases like PubMed, EMBASE, and ClinicalTrial.gov. The quality assessment was done using the Cochrane Risk of Bias Tool. We utilized a random effect meta-analysis to calculate risk ratio (RR) with 95% confidence intervals (CI). The Open Vigil 2.1 MedDRAv24 was used to search the FAERS database, with data available until September 2023. The disproportionality was calculated using the proportional reporting ratio and the reporting odds ratio. The study protocol for meta-analysis was registered with PROSPERO; CRD42022378006. For the safety meta-analysis, seven RCTs with available AEs were examined. A total of 942 AEs were found associated with the venetoclax group; 79% of them were in grade three or above. Venetoclax significantly increased the risk of neutropenia grade three or above (RR = 1.34, 95% CI: 1.10-1.64, p: 0.0033) compared with the control group. In FAERS, 26,436 patients were reported with AEs associated with venetoclax. Significant signal scores were observed in hematological, cardiac, vascular, and gastrointestinal disorders. 11 out of 30 generated signals, failed to meet the signal criteria upon refinement. The current study updated and improved the safety profile of venetoclax in the post-marketing period, assisting in risk evaluation and mitigation for the best possible patient health care.
人们仍然对 venetoclax 在更大人群中的长期安全性表示关注,因为关于罕见和迟发性不良事件 (AE) 的证据有限。该研究整合了来自随机对照试验 (RCT) 和美国食品药品监督管理局不良事件监测系统 (FAERS) 的 venetoclax 在白血病患者中的安全性数据。我们系统地检索了在任何性别、单药或联合治疗的成年白血病患者中报告 venetoclax 安全性结局的 RCT 报告,在 PubMed、EMBASE 和 ClinicalTrials.gov 等数据库中应用高级搜索。使用 Cochrane 风险偏倚工具进行质量评估。我们使用随机效应荟萃分析计算风险比 (RR) 和 95%置信区间 (CI)。使用 Open Vigil 2.1 MedDRAv24 搜索 FAERS 数据库,数据可追溯到 2023 年 9 月。使用比例报告比和报告比值比计算比例失调。荟萃分析的研究方案已在 PROSPERO 上注册;CRD42022378006。对于安全性荟萃分析,检查了有可用 AE 的七项 RCT。共发现与 venetoclax 组相关的 942 种 AE;其中 79%为三级或以上。与对照组相比,venetoclax 显著增加了三级或以上中性粒细胞减少症的风险 (RR=1.34,95%CI:1.10-1.64,p:0.0033)。在 FAERS 中,报告了 26436 名与 venetoclax 相关的 AE 患者。观察到血液学、心脏、血管和胃肠道疾病的显著信号评分。在生成的 30 个信号中,有 11 个经过细化后未能达到信号标准。本研究在上市后时期更新和改善了 venetoclax 的安全性概况,有助于进行风险评估和缓解,以实现最佳的患者医疗保健。