Baz Rachid, Li Liang, Kottke-Marchant Kandice, Srkalovic Gordan, McGowan Bridget, Yiannaki Erin, Karam Mary Ann, Faiman Beth, Jawde Rony Abou, Andresen Steven, Zeldis Jerome, Hussein Mohamad A
Cleveland Clinic Myeloma Research Program, Cleveland Clinic Foundation, OH 44195, USA.
Mayo Clin Proc. 2005 Dec;80(12):1568-74. doi: 10.4065/80.12.1568.
To study the efficacy of daily low-dose aspirin (81 mg orally) in decreasing the incidence of venous thromboembolic events (VTEs) in patients with multiple myeloma receiving pegylated doxorubicin, vincristine, and decreased-frequency dexamethasone, plus thalidomide (DVd-T).
In this phase 2 clinical trial of DVd-T, conducted by the Cleveland Clinic Foundation from August 2001 to October 2003, 105 patients were enrolled. The first 35 patients experienced increased numbers of VTEs. von Willebrand levels and platelet aggregation to ristocetin before and after treatment with DVd-T increased significantly, suggesting a pathophysiology involving platelet-endothelial interaction. Aspirin was added to the regimen, thus generating 3 patient groups: group 1 received aspirin from the start of DVd-T treatment before the study began (58 patients), group 2 received aspirin after the start of DVd-T treatment and after the study began (26 patients), and group 3 did not receive daily low-dose aspirin during the study (19 patients). Two patients being treated with warfarin for other indications were excluded from the study. The primary end point for this study was the incidence of VTE in the form of either deep venous thrombosis or pulmonary embolism. Secondary end points were the time to the first VTE, time to the composite end point of death or first VTE, and incidence of bleeding complications.
After a median follow-up of 24 months, on an intent-to-treat basis, 26 posttreatment VTEs occurred after a median of 90 days, with 19% occurring in group 1, 15% in group 2, and 58% in group 3. Following multivariate time-to-event analysis, aspirin use continued to be associated with lower relative risk of VTE (hazard ratio, 0.22; confidence interval, 0.10-0.47; P<.001) and of the composite end point (hazard ratio, 0.28; confidence interval, 0.15-0.51; P<.001).
Daily low-dose aspirin (81 mg orally) given to patients with newly diagnosed and relapsed/refractory multiple myeloma who were receiving DVd-T reduced the incidence of VTEs without an increase in bleeding complications.
研究每日口服低剂量阿司匹林(81毫克)对接受聚乙二醇化阿霉素、长春新碱、低频率地塞米松联合沙利度胺(DVd-T)治疗的多发性骨髓瘤患者静脉血栓栓塞事件(VTE)发生率的影响。
本2期DVd-T临床试验由克利夫兰诊所基金会于2001年8月至2003年10月开展,共纳入105例患者。前35例患者的VTE数量增加。DVd-T治疗前后的血管性血友病因子水平及瑞斯托霉素诱导的血小板聚集显著增加,提示存在涉及血小板-内皮相互作用的病理生理学机制。阿司匹林被添加到治疗方案中,从而产生3组患者:第1组在研究开始前DVd-T治疗开始时即服用阿司匹林(58例患者),第2组在DVd-T治疗开始后且研究开始后服用阿司匹林(26例患者),第3组在研究期间未每日服用低剂量阿司匹林(19例患者)。2例因其他指征正在接受华法林治疗的患者被排除在研究之外。本研究的主要终点是以深静脉血栓形成或肺栓塞形式出现的VTE发生率。次要终点为首次发生VTE的时间、死亡或首次发生VTE的复合终点时间以及出血并发症的发生率。
中位随访24个月后,在意向性治疗基础上,治疗后发生26例VTE,中位时间为90天,其中第1组发生率为19%,第2组为15%,第3组为58%。多变量事件发生时间分析显示,使用阿司匹林仍与较低的VTE相对风险(风险比,(0.22);置信区间,(0.10 - 0.47);(P < 0.001))以及复合终点相对风险(风险比,(0.28);置信区间,(0.15 - 0.51);(P < 0.001))相关。
对于接受DVd-T治疗的新诊断及复发/难治性多发性骨髓瘤患者,每日口服低剂量阿司匹林(81毫克)可降低VTE发生率,且不增加出血并发症。