Department of Clinical Pharmacology and Therapeutics, Asan Medical Center, University of Ulsan, Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea.
Clinical Pharmacology, Global Product Development, Pfizer, 10555 Science Center Dr., San Diego, California, 92121, USA.
AAPS J. 2019 Jan 30;21(2):22. doi: 10.1208/s12248-018-0290-x.
Prediction of survival endpoints, e.g., overall survival (OS) and progression-free survival (PFS), based on early observations, i.e., tumor size, may facilitate early decision making in oncology drug development. In this paper, using data from six randomized trials for first- or second-line advanced breast cancer (ABC) treatments with various mechanisms of action, tumor size change from baseline at different observation time points was evaluated as a predictor for survival endpoints using different modeling approaches. The aim is to establish a predictive model where tumor size change from baseline can be used as a treatment independent predictive marker for PFS and OS in first- and second-line ABC. The results showed that tumor size change at single time point (TSP) or up to certain time points as a time-varying covariate (TSTVC) were significant predictors for OS and PFS in the survival models along with other covariates identified for each line of treatment. TSP and TSTVC models performed similarly for first-line treatments; TSTVC performed significantly better for second-line treatments. Eight weeks was selected as the recommended early evaluation time of tumor size change to predict OS and PFS in both first- and second-line treatment, while better prediction can be achieved for first-line OS by using 16 weeks tumor size change. The result of this study is treatment independent and can be used to predict the outcome of the clinical trials using early readout of tumor size change for the classes of drugs that have been evaluated in this study.
基于早期观察结果(例如肿瘤大小)预测生存终点,例如总生存期(OS)和无进展生存期(PFS),可能有助于肿瘤药物研发的早期决策。本文使用来自六个针对不同作用机制的一线或二线晚期乳腺癌(ABC)治疗的随机试验数据,通过不同的建模方法评估基线时肿瘤大小变化作为生存终点的预测因子。目的是建立一个预测模型,其中基线时肿瘤大小的变化可以作为一线和二线 ABC 中 PFS 和 OS 的独立预测标志物。结果表明,在生存模型中,单一时间点(TSP)或特定时间点的肿瘤大小变化(TSTVC)作为时变协变量,与为每种治疗线确定的其他协变量一起,是 OS 和 PFS 的重要预测因子。TSP 和 TSTVC 模型在一线治疗中表现相似;TSTVC 在二线治疗中表现明显更好。8 周被选为推荐的肿瘤大小变化早期评估时间,以预测一线和二线治疗的 OS 和 PFS,而通过使用 16 周肿瘤大小变化可以实现一线 OS 的更好预测。本研究的结果是独立于治疗的,可以用于预测使用本研究中评估的药物类别进行的临床试验的结果。