Bruton tyrosine kinase inhibitor monotherapy in B-cell lymphoma and risk of infection: A systematic review and meta-analysis of randomized controlled trials

IF 3.3 4区 医学 Q2 HEMATOLOGY Hematological Oncology Pub Date : 2024-09-12 DOI:10.1002/hon.3308
Mohammed Zuber, Samruddhi Nandkumar Borate, Pooja Gokhale, Akhila Yerubandi, N. M. Mahmudul Alam Bhuiya, Smita Rawal, Henry N. Young, Lorenzo Villa Zapata
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Abstract

Bruton's tyrosine kinase (BTK) inhibitors are important therapeutic advances with promising efficacy outcomes in the treatment of patients with chronic lymphocytic leukemia and other B-cell lymphoma subtypes. However, the utility of BTK inhibitors can be limited by adverse events such as infections. In this systematic review and meta-analysis, we aim to determine the risk of various infections associated with BTK inhibitor monotherapy in B-cell lymphoma patients. A comprehensive search was conducted in MEDLINE/PubMed, Embase, and Web of Science databases from their inception until October 2023. ClinicalTrials.gov, bibliographies, and relevant conference abstracts were also searched for additional records. Randomized controlled trials that included any B-cell lymphoma patients treated with BTK inhibitor monotherapy and reported infection were included. Meta-analysis was performed to calculate risk ratio (RR) using a random-effects model in R Statistical Software, version 4.3.2. Of 3292 studies retrieved, we included 12 studies in this systematic review and meta-analysis. The median age of patients across the study arms ranged between 64 and 73 years. The overall pooled RR for any grade upper respiratory tract infections (URTI) associated with BTK inhibitor treatment was 1.55 (95% Confidence Interval (CI) 1.22–1.97). The RR of grade ≥3 URTI was reported in 14 out of 1046 patients, yielding an RR of 1.46 (95% CI 0.61–3.54), which was not statistically significant. The pooled RR of any grade pneumonia was 1.20 (95% CI 0.68–2.10) and grade ≥3 pneumonia was 1.12 (95% CI 0.67–1.85), both of which were not statistically significant. Patients with B-cell lymphoma who are undergoing BTK inhibitor monotherapy face an elevated risk of developing URTI. Clinicians prescribing BTK inhibitors should be aware of the potential infectious events that may occur. Close monitoring and the implementation of effective prophylactic measures are essential for managing these patients.

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布鲁顿酪氨酸激酶抑制剂单药治疗B细胞淋巴瘤与感染风险:随机对照试验的系统回顾和荟萃分析
布鲁顿酪氨酸激酶(BTK)抑制剂是治疗慢性淋巴细胞白血病和其他 B 细胞淋巴瘤亚型患者的重要疗法,其疗效令人鼓舞。然而,BTK 抑制剂的作用可能会受到感染等不良反应的限制。在本系统综述和荟萃分析中,我们旨在确定B细胞淋巴瘤患者在接受BTK抑制剂单药治疗时发生各种感染的风险。我们在 MEDLINE/PubMed、Embase 和 Web of Science 数据库中进行了全面检索,检索时间从开始到 2023 年 10 月。此外,还检索了 ClinicalTrials.gov、参考书目和相关会议摘要,以获取更多记录。纳入了任何接受 BTK 抑制剂单药治疗的 B 细胞淋巴瘤患者并报告感染情况的随机对照试验。我们使用 4.3.2 版 R 统计软件中的随机效应模型进行了 Meta 分析,以计算风险比 (RR)。在检索到的 3292 项研究中,我们将 12 项研究纳入了本次系统综述和荟萃分析。各研究臂的患者年龄中位数介于 64 岁至 73 岁之间。与 BTK 抑制剂治疗相关的任何级别上呼吸道感染(URTI)的总体汇总 RR 为 1.55(95% 置信区间 (CI) 1.22-1.97)。1046例患者中有14例报告了≥3级URTI的RR,RR为1.46(95% CI 0.61-3.54),无统计学意义。任何等级肺炎的总RR为1.20(95% CI 0.68-2.10),≥3级肺炎的总RR为1.12(95% CI 0.67-1.85),两者均无统计学意义。接受BTK抑制剂单药治疗的B细胞淋巴瘤患者罹患URTI的风险较高。开具 BTK 抑制剂处方的临床医生应了解可能发生的潜在感染事件。密切监测并实施有效的预防措施对于管理这些患者至关重要。
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来源期刊
Hematological Oncology
Hematological Oncology 医学-血液学
CiteScore
4.20
自引率
6.10%
发文量
147
审稿时长
>12 weeks
期刊介绍: Hematological Oncology considers for publication articles dealing with experimental and clinical aspects of neoplastic diseases of the hemopoietic and lymphoid systems and relevant related matters. Translational studies applying basic science to clinical issues are particularly welcomed. Manuscripts dealing with the following areas are encouraged: -Clinical practice and management of hematological neoplasia, including: acute and chronic leukemias, malignant lymphomas, myeloproliferative disorders -Diagnostic investigations, including imaging and laboratory assays -Epidemiology, pathology and pathobiology of hematological neoplasia of hematological diseases -Therapeutic issues including Phase 1, 2 or 3 trials as well as allogeneic and autologous stem cell transplantation studies -Aspects of the cell biology, molecular biology, molecular genetics and cytogenetics of normal or diseased hematopoeisis and lymphopoiesis, including stem cells and cytokines and other regulatory systems. Concise, topical review material is welcomed, especially if it makes new concepts and ideas accessible to a wider community. Proposals for review material may be discussed with the Editor-in-Chief. Collections of case material and case reports will be considered only if they have broader scientific or clinical relevance.
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