Mangal Naveen, Salem Ahmed Hamed, Menon Rajeev M, Freise Kevin J
Center for Pharmacometrics and Systems Pharmacology, University of Florida, Orlando, FL, USA.
Abbvie, Inc., North Chicago, IL, USA.
Hematol Oncol. 2018 Apr 19. doi: 10.1002/hon.2514.
Progression-free survival (PFS) is the standard endpoint for demonstration of clinical effectiveness of novel therapies in relapsed or refractory multiple myeloma (RRMM). However, the long evaluation times for PFS limits its usefulness in the development of new therapies. Therefore, the objective of this analysis was to determine the relationship between response rates and median PFS in RRMM. A database was systematically developed from 268 identified RRMM trials reported from 1999 to 2016. Evaluated covariates for the relationship between response rates and PFS included age, sex, drug class(es), and number of drug classes. One-hundred two (102) trials involving 136 cohorts were included in the meta-analysis, representing 13 322 patients in total. Regression analysis using response rates and median PFS indicated that the correlation between very good partial response (VGPR) or better and median PFS was higher (R = 0.63) than the separately analyzed correlations between clinical benefit, overall response, or complete response rate and median PFS (R = 0.47 - 0.52). Subsequent covariate analysis revealed that treatment with an immunomodulatory imide drug (IMiD) further improved the relationship (R = 0.69), with a longer median PFS at a given VGPR or better rate when at least 1 drug treatment was an IMiD. Number of drug classes was not found to alter this relationship. In conclusion, VGPR or better rate can be used to predict the median PFS, with adjustment for the additional PFS provided by an IMiD.
无进展生存期(PFS)是证明新型疗法对复发或难治性多发性骨髓瘤(RRMM)临床有效性的标准终点。然而,PFS的评估时间较长,限制了其在新疗法研发中的作用。因此,本分析的目的是确定RRMM中缓解率与中位PFS之间的关系。我们系统地建立了一个数据库,该数据库来自1999年至2016年报告的268项已识别的RRMM试验。评估缓解率与PFS之间关系的协变量包括年龄、性别、药物类别和药物类别数量。荟萃分析纳入了涉及136个队列的102项试验,总共代表13322名患者。使用缓解率和中位PFS的回归分析表明,非常好的部分缓解(VGPR)或更好与中位PFS之间的相关性更高(R = 0.63),高于单独分析的临床获益、总缓解或完全缓解率与中位PFS之间的相关性(R = 0.47 - 0.52)。随后的协变量分析显示,使用免疫调节性酰亚胺药物(IMiD)治疗进一步改善了这种关系(R = 0.69),当至少一种药物治疗为IMiD时,在给定的VGPR或更好缓解率下,中位PFS更长。未发现药物类别数量会改变这种关系。总之,VGPR或更好的缓解率可用于预测中位PFS,并根据IMiD提供的额外PFS进行调整。