Mock Joseph, Kunk Paul R, Palkimas Surabhi, Sen Jeremy M, Devitt Michael, Horton Bethany, Portell Craig A, Williams Michael E, Maitland Hillary
Division of Hematology-Oncology, Department of Medicine and Cancer Center, University of Virginia Health System, Charlottesville, VA.
Division of Hematology-Oncology, Department of Medicine and Cancer Center, University of Virginia Health System, Charlottesville, VA.
Clin Lymphoma Myeloma Leuk. 2018 Nov;18(11):755-761. doi: 10.1016/j.clml.2018.07.287. Epub 2018 Aug 1.
The Bruton tyrosine kinase inhibitor, ibrutinib, is an effective therapy against mature B-cell malignancies. Although generally well tolerated, serious bleeding emerged during developmental clinical trials as an unexpected, although uncommon, adverse event. As the use of ibrutinib increases outside of the clinical trial setting and in patients with more comorbidities, the rate of major bleeding could be greater.
A retrospective analysis the data from all patients at our center and its regional clinics who had been prescribed ibrutinib from January 2012 to May 2016 were reviewed for demographic data, comorbid illnesses, bleeding events, and concurrent medications.
We identified 70 patients. Bleeding of any grade occurred in 56% of patients, mostly grade 1 to 2 bruising and epistaxis. Major bleeding, defined as grade ≥ 3, occurred in 19% of patients, greater than previously reported. Anemia (hemoglobin < 12 g/dL; hazard ratio [HR], 5.0; 95% confidence interval [CI], 1.4-18.2; P = .02) and an elevated international normalized ratio (> 1.5; HR, 9.5; 95% CI, 2.7-33.5; P < .01) at ibrutinib initiation were associated with an increased risk of major bleeding. Of those with major bleeding, most patients were also taking an antiplatelet agent (70%), an anticoagulant (17%), or a CYP 3A4 inhibitor (7%), with 13% taking both antiplatelet and anticoagulant medications. The use of both antiplatelet and anticoagulant therapy significantly increased the risk of a major bleed event (HR, 19.2; 95% CI, 2.3-166.7; P < .01).
The results of the present study have demonstrated a greater rate of major bleeding with ibrutinib use in a standard clinical setting than previously reported. Patients with anemia or an elevated international normalized ratio or requiring anticoagulant and/or antiplatelet medications during ibrutinib therapy have a significantly increased risk of major bleeding. Careful consideration of the risks and benefits for this population is needed. The combination of antiplatelet and anticoagulation medications with ibrutinib therapy is of particular concern.
布鲁顿酪氨酸激酶抑制剂依鲁替尼是一种治疗成熟B细胞恶性肿瘤的有效疗法。尽管总体耐受性良好,但在临床开发试验期间出现了严重出血这一意外的不良事件,不过并不常见。随着依鲁替尼在临床试验环境之外以及合并症更多的患者中使用增加,严重出血的发生率可能更高。
对2012年1月至2016年5月期间在我们中心及其地区诊所所有开具依鲁替尼处方的患者数据进行回顾性分析,以获取人口统计学数据、合并症、出血事件及同时使用的药物信息。
我们共纳入70例患者。56%的患者发生了任何级别的出血,主要为1至2级瘀斑和鼻出血。定义为≥3级的严重出血发生在19%的患者中,高于先前报道。开始使用依鲁替尼时贫血(血红蛋白<12 g/dL;风险比[HR],5.0;95%置信区间[CI],1.4 - 18.2;P = .02)和国际标准化比值升高(>1.5;HR,9.5;95% CI,2.7 - 33.5;P < .01)与严重出血风险增加相关。在发生严重出血的患者中,大多数患者还在服用抗血小板药物(70%)、抗凝剂(17%)或CYP 3A4抑制剂(7%),13%的患者同时服用抗血小板和抗凝药物。同时使用抗血小板和抗凝治疗显著增加了严重出血事件的风险(HR,19.2;95% CI,2.3 - 166.7;P < .01)。
本研究结果表明,在标准临床环境中使用依鲁替尼时严重出血的发生率高于先前报道。贫血或国际标准化比值升高的患者,或在依鲁替尼治疗期间需要抗凝和/或抗血小板药物的患者,严重出血风险显著增加。需要仔细权衡该人群的风险和获益。抗血小板和抗凝药物与依鲁替尼联合治疗尤其值得关注。