伊鲁替尼在复发或难治性慢性淋巴细胞白血病患者中的实际结果:临床研究的荟萃分析

IF 2.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
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引用次数: 0

摘要

背景:慢性淋巴细胞白血病(CLL)是一种主要诊断于老年人的b细胞恶性肿瘤。对于年轻患者,治疗方案通常包括基于氟达拉滨、环磷酰胺和利妥昔单抗的方案;然而,至少有20%的患者对这些疗法表现出耐药性。Ibrutinib是一种共价布鲁顿酪氨酸激酶(BTK)抑制剂,与传统治疗相比,已证明安全性更高。这项荟萃分析检验了依鲁替尼治疗复发/难治性CLL的有效性和安全性。方法:利用相关关键词在PubMed、Scopus、谷歌Scholar等在线数据库中进行综合检索。提取与完全缓解(CR)、总缓解率(ORR)和不良事件相关的数据,以评估依鲁替尼治疗的有效性和安全性。结果以森林样地呈现,以95%置信区间(CI)显示事件发生率和风险比,同时使用I²统计量评估异质性。采用漏斗图从视觉上检验潜在的发表偏倚。结果:本荟萃分析纳入了21项研究。伊鲁替尼作为单药治疗与9%的完全缓解率(CR) (95% CI: 5-14%)和77%的总缓解率(ORR) (95% CI: 70-83%)相关。与其他药物联合使用时,伊鲁替尼的CR率为21% (95% CI: 9-41%), ORR为84% (95% CI: 80-88%)。不良事件与治疗结果无显著相关。漏斗图显示没有显著的发表偏倚。结论:单药伊鲁替尼已被证明是治疗复发/难治性CLL患者的有效方法。然而,伊鲁替尼与其他药物联合使用已显示出增强的治疗效果。需要进一步的研究来彻底评估这种治疗方案的安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real world results of ibrutinib in patients with relapsed or refractory chronic lymphocytic leukemia: a meta-analysis of clinical studies.

Background: Chronic lymphocytic leukemia (CLL) is a B-cell malignancy primarily diagnosed in older adults. For younger patients, treatment options often include regimens based on fludarabine, cyclophosphamide, and rituximab; however, at least 20% of patients exhibit resistance to these therapies. Ibrutinib, a covalent Bruton's tyrosine kinase (BTK) inhibitor, has demonstrated enhanced safety compared to conventional treatments. This meta-analysis examines the efficacy and safety of ibrutinib in managing relapsed/refractory CLL.

Method: Relevant keywords were used to conduct a comprehensive search across online databases, including PubMed, Scopus, and Google Scholar. Data related to complete response (CR), overall response rate (ORR), and adverse events were extracted to evaluate the efficacy and safety of ibrutinib treatment. The results were presented in forest plots illustrating event rates and risk ratios with 95% confidence intervals (CI), while heterogeneity was assessed using I² statistics. Funnel plots were employed to examine potential publication bias visually.

Result: Twenty-one studies were included in this meta-analysis. Ibrutinib as a single-agent treatment was associated with a 9% complete response (CR) rate (95% CI: 5-14%) and a 77% overall response rate (ORR) (95% CI: 70-83%). When combined with other agents, ibrutinib achieved a CR rate of 21% (95% CI: 9-41%) and an ORR of 84% (95% CI: 80-88%). Adverse events were not significantly correlated with treatment outcomes. Funnel plots indicated no significant publication bias.

Conclusion: Single-agent ibrutinib has proven to be an effective therapy for patients with relapsed/refractory CLL. However, combining ibrutinib with other agents has demonstrated enhanced treatment efficacy. Further studies are needed to evaluate the safety profile of this therapeutic regimen thoroughly.

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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACYTOXICOLOGY&nb-TOXICOLOGY
CiteScore
4.80
自引率
0.00%
发文量
87
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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