Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA.
Biostatistics, Roche Products Ltd, Welwyn Garden City, UK.
Br J Haematol. 2022 Jul;198(2):333-337. doi: 10.1111/bjh.18217. Epub 2022 May 2.
Progression-free survival (PFS) has been the regulatory primary end-point for recent phase III trials in first-line follicular lymphoma (FL), but requires prolonged follow-up. Complete response (CR) at 30 months after initiation of induction treatment was validated as surrogate end-point for PFS. Our objective was to further evaluate surrogacy of CR measured by [ F] fluorodeoxyglucose (FDG) positron emission tomography (PET) imaging at the end of induction (EoI). Individual patient data were analysed from 1505 patients from five randomized trials. Trial-level surrogacy examining the association between treatment effects on EoI-PET-CR and PFS was evaluated using linear regression ( ) and bivariate Copula ( ) models. Although EoI-PET-CR strongly predicted PFS at a prognostic level, the trial-level assessment did not show strong correlation ( , confidence interval [CI]: 0.20-0.88; , CI: 0.0-0.82). The high uncertainty in estimation was possibly due to the small number of trials and the population of patients with available PET data. Maintenance therapy affecting PFS beyond induction treatment, but not EoI-PET-CR end-point, may have distorted the association between treatment effects. However, there will probably be a number of additional trials approaching completion with available PET response data. Refined evaluation of PET-CR based surrogate end-points is still warranted.
无进展生存期(PFS)一直是滤泡性淋巴瘤(FL)一线治疗中最近的 III 期试验的监管主要终点,但需要长期随访。诱导治疗开始后 30 个月的完全缓解(CR)已被验证为 PFS 的替代终点。我们的目的是进一步评估诱导结束时(EoI)[ F]氟脱氧葡萄糖(FDG)正电子发射断层扫描(PET)成像测量的 CR 的替代作用。从五项随机试验中对 1505 名患者的个体患者数据进行了分析。使用线性回归( )和双变量 Copula( )模型评估了 EoI-PET-CR 和 PFS 之间治疗效果关联的试验水平替代作用。虽然 EoI-PET-CR 在预后水平上强烈预测 PFS,但试验水平评估并未显示出强烈的相关性( ,置信区间[CI]:0.20-0.88; ,CI:0.0-0.82)。估计的高度不确定性可能是由于试验数量较少且具有可用 PET 数据的患者人群。维持治疗可能会影响诱导治疗以外的 PFS,但不会影响 EoI-PET-CR 终点,这可能会扭曲治疗效果之间的关联。然而,可能会有许多其他试验接近完成并提供可用的 PET 反应数据。仍需要对基于 PET-CR 的替代终点进行精细评估。