Bröckelmann P J, Müller H, Fuchs M, Gillessen S, Eichenauer D A, Borchmann S, Jacob A S, Behringer K, Momotow J, Ferdinandus J, Böll B, Yang X, Kobe C, Eich H-T, Baues C, Klapper W, Engert A, Borchmann P, von Tresckow B
University of Cologne, Faculty of Medicine and University Hospital of Cologne, Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Düsseldorf (CIO ABCD) and German Hodgkin Study Group (GHSG), Cologne, Germany.
Merck & Co., Inc., Rahway, USA.
Ann Oncol. 2025 Apr;36(4):393-402. doi: 10.1016/j.annonc.2024.12.009. Epub 2024 Dec 18.
This study aimed to evaluate the correlation between progression-free (PFS) and overall survival (OS) after first-line treatment of classical Hodgkin lymphoma (HL) and to assess the potential of PFS as a surrogate parameter for OS.
We analyzed individual patient data collected during and after treatment with polychemotherapy in nine randomized phase III trials [German Hodgkin Study Group (GHSG) HD7-HD15] between January 1993 and August 2018. The effects of 16 experimental treatments on PFS and OS at the trial level were evaluated using Cox proportional hazards (PH) regression and linear weighted least squares regression. At the patient level, marginal Cox PH models for multiple endpoints were applied using the Wei-Lin-Weissfeld method.
At least one PFS and OS event was recorded in 1682 and 1064 of 10 605 patients, respectively. At the trial level, there was a strong correlation between treatment effects on PFS and OS (weighted Pearson r = 0.72, R = 0.54, P < 0.001). At the patient level, a moderate to strong correlation between treatment effects on PFS and OS was observed, with Pearson r values ranging between 0.61 and 0.85 (each P < 0.001) and an overall r = 0.74. A regression model that accounted for different types of experimental treatments and historical progress across trial generations achieved a very strong correlation (R = 0.93). When applied to data from the contemporary first-line ECHELON-1 trial, this model successfully predicted OS from PFS {prognosticated ln[HR(OS)] = -0.68 as compared with observed ln[HR(0.59)] = -0.53}.
In first-line trials of HL, PFS and OS, as well as treatment effects and prognostic effects on these endpoints, are strongly correlated. PFS serves as a strong predictor of treatment effects on OS, providing valuable insights many years before OS can be reliably assessed.
本研究旨在评估经典型霍奇金淋巴瘤(HL)一线治疗后的无进展生存期(PFS)与总生存期(OS)之间的相关性,并评估PFS作为OS替代参数的潜力。
我们分析了1993年1月至2018年8月期间在9项随机III期试验[德国霍奇金淋巴瘤研究组(GHSG)HD7-HD15]中接受多药化疗期间及之后收集的个体患者数据。使用Cox比例风险(PH)回归和线性加权最小二乘回归评估了16种实验性治疗在试验水平上对PFS和OS的影响。在患者水平上,使用Wei-Lin-Weissfeld方法应用多终点边际Cox PH模型。
在10605例患者中,分别有1682例和1064例记录了至少1次PFS和OS事件。在试验水平上,治疗对PFS和OS的影响之间存在强相关性(加权Pearson r = 0.72,R = 0.54,P < 0.001)。在患者水平上,观察到治疗对PFS和OS的影响之间存在中度至强相关性,Pearson r值在0.61至0.85之间(均P < 0.001),总体r = 0.74。一个考虑了不同类型实验性治疗和各试验代历史进展的回归模型实现了非常强的相关性(R = 0.93)。当应用于当代一线ECHELON-1试验的数据时,该模型成功地从PFS预测了OS{预测的ln[HR(OS)] = -0.68,而观察到的ln[HR(0.59)] = -0.53}。
在HL的一线试验中,PFS和OS以及对这些终点的治疗效果和预后效果密切相关。PFS可作为治疗对OS影响的有力预测指标,在OS能够可靠评估的多年前提供有价值的见解。