Burke John M, van der Jagt Richard H C, Flinn Ian W, Craig Michael D, Chen Ling, Morganroth Joel, Munteanu Mihaela C, MacDonald David A
Rocky Mountain Cancer Centers, 1700 S. Potomac Street, Aurora, CO, 80012, USA,
Cancer Chemother Pharmacol. 2015 Jul;76(1):211-6. doi: 10.1007/s00280-015-2776-x. Epub 2015 May 26.
Bendamustine is used in chronic lymphocytic leukemia (first-line) and indolent B-cell non-Hodgkin lymphoma (NHL) that progressed during/within 6 months of treatment with rituximab or a rituximab-containing regimen. This study was a postapproval commitment to investigate bendamustine's effect on cardiac repolarization in treatment-naïve adults with advanced indolent NHL/mantle cell lymphoma (MCL).
In this multicenter, open-label, phase 3 study, patients received 6-8 28-day cycles of bendamustine (90 mg/m(2), days 1 and 2) and rituximab (375 mg/m(2), day 1). Exclusions included a history of cardiac conditions with potential for QT prolongation. The primary endpoint was change in Fridericia-corrected QT (QTcF; 3 electrocardiograms per time point) on day 2 of cycle 1, from just before infusion to end of infusion (immediately postinfusion, coinciding with maximum plasma concentration of bendamustine). Change 1 h postinfusion was also measured. Exploratory assessments included specific QTcF outlier analyses (new QTcF >500 ms, change >60 ms) and morphological changes.
Of the 54 enrolled patients (mean age, 62.9 years), 53 received ≥1 dose; 49 completed ≥6 cycles. Mean QTcF change from baseline was 6.7 ms at end of infusion; no mean changes >20 ms were detected ≤1 h postinfusion. No patients met specific outlier criteria at end of infusion or 1 h postinfusion. No morphological changes were detected.
In this small treatment-naïve population with advanced NHL/MCL, bendamustine did not produce a clinically relevant increase in mean QTcF on the second infusion day. The potential for delayed effects on QT interval after 1 h was not evaluated.
苯达莫司汀用于治疗慢性淋巴细胞白血病(一线治疗)以及在使用利妥昔单抗或含利妥昔单抗方案治疗期间/6个月内病情进展的惰性B细胞非霍奇金淋巴瘤(NHL)。本研究是一项批准后承诺研究,旨在调查苯达莫司汀对初治晚期惰性NHL/套细胞淋巴瘤(MCL)成年患者心脏复极的影响。
在这项多中心、开放标签的3期研究中,患者接受6 - 8个28天周期的苯达莫司汀(90mg/m²,第1天和第2天)和利妥昔单抗(375mg/m²,第1天)治疗。排除标准包括有QT间期延长潜在风险的心脏病史。主要终点是第1周期第2天从输注前到输注结束(输注后即刻,与苯达莫司汀的最大血浆浓度一致)时的弗里德里西亚校正QT(QTcF;每个时间点3份心电图)变化。还测量了输注后1小时的变化。探索性评估包括特定的QTcF异常值分析(新的QTcF>500ms,变化>60ms)和形态学变化。
在54例入组患者(平均年龄62.9岁)中,53例接受了≥1剂治疗;49例完成了≥6个周期。输注结束时,QTcF较基线的平均变化为6.7ms;输注后≤1小时未检测到平均变化>20ms。输注结束时或输注后1小时无患者符合特定的异常值标准。未检测到形态学变化。
在这个初治的晚期NHL/MCL小群体中,苯达莫司汀在第2次输注日未导致QTcF均值出现具有临床意义的增加。未评估1小时后对QT间期的延迟影响。