Parikh Apurvasena, Gopalakrishnan Sathej, Freise Kevin J, Verdugo Maria E, Menon Rajeev M, Mensing Sven, Salem Ahmed Hamed
a Clinical Pharmacology and Pharmacometrics , Abbvie Inc , North Chicago , IL , USA.
b Pharmacometrics , AbbVie Deutschland GmbH & Co KG , Ludwigshafen , Germany.
Leuk Lymphoma. 2018 Apr;59(4):871-879. doi: 10.1080/10428194.2017.1361024. Epub 2017 Aug 10.
Exposure-response analyses were performed for a venetoclax monotherapy study in 106 patients with varying subtypes of non-Hodgkin lymphoma (NHL) (NCT01328626). Logistic regression, time-to-event, and progression-free survival (PFS) analyses were used to evaluate the relationship between venetoclax exposure, NHL subtype and response, PFS, or occurrence of serious adverse events. Trends for small increases in the probability of response with increasing venetoclax exposures were identified, and became more evident when assessed by NHL subtype. Trends in exposure-PFS were shown for the mantle cell lymphoma (MCL) subtype, but not other subtypes. There was no increase in the probability of experiencing a serious adverse event with increasing exposure. Overall, the results indicate that venetoclax doses of 800-1200 mg as a single agent may be appropriate to maximize efficacy in MCL, follicular lymphoma, and diffuse large B-cell lymphoma subtypes with no expected negative impact on safety.
对一项在106例不同亚型非霍奇金淋巴瘤(NHL)患者中开展的维奈托克单药治疗研究(NCT01328626)进行了暴露-反应分析。采用逻辑回归、事件发生时间和无进展生存期(PFS)分析来评估维奈托克暴露量、NHL亚型与反应、PFS或严重不良事件发生之间的关系。确定了随着维奈托克暴露量增加反应概率略有增加的趋势,按NHL亚型评估时该趋势更为明显。显示了套细胞淋巴瘤(MCL)亚型的暴露-PFS趋势,但其他亚型未显示。随着暴露量增加,发生严重不良事件的概率没有增加。总体而言,结果表明,800-1200mg的维奈托克单药剂量可能适合使MCL、滤泡性淋巴瘤和弥漫性大B细胞淋巴瘤亚型的疗效最大化,且对安全性无预期负面影响。