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利用混合肿瘤生长动态模型将肿瘤生长动力学与接受伊匹单抗治疗的晚期黑色素瘤患者的生存情况联系起来。

Linking Tumor Growth Dynamics to Survival in Ipilimumab-Treated Patients With Advanced Melanoma Using Mixture Tumor Growth Dynamic Modeling.

机构信息

Clinical Pharmacology and Pharmacometrics, Bristol-Myers Squibb, Princeton, New Jersey, USA.

Metrum Research Group, Tariffville, Connecticut, USA.

出版信息

CPT Pharmacometrics Syst Pharmacol. 2019 Nov;8(11):825-834. doi: 10.1002/psp4.12454. Epub 2019 Aug 13.

Abstract

Early tumor assessments have been widely used to predict overall survival (OS), with potential application to dose selection and early go/no-go decisions. Most published tumor dynamic models assume a uniform pattern of tumor growth dynamics (TGDs). We developed a mixture TGD model to characterize different patterns of longitudinal tumor sizes. Data from 688 patients with advanced melanoma who received ipilimumab 3 or 10 mg/kg every 3 weeks in a phase III study (NCT01515189) were used in a TGD-OS analysis. The mixture model described TGD profiles using three subpopulations (no-growth, intermediate, and fast). The TGD model showed a positive exposure/dose-response (i.e., a higher proportion of patients in no/intermediate growth subpopulations and a lower tumor growth rate with ipilimumab 10 mg/kg relative to the 3 mg/kg dose). Finally, the mixture TGD model-based measures of tumor response provided better predictions of OS compared with the nonmixture model.

摘要

早期肿瘤评估已被广泛用于预测总生存期(OS),具有用于选择剂量和早期进行/停止决策的潜力。大多数已发表的肿瘤动力学模型假设肿瘤生长动力学(TGD)呈均匀模式。我们开发了一种混合 TGD 模型来描述纵向肿瘤大小的不同模式。在一项 III 期研究(NCT01515189)中,使用了 688 名接受每 3 周 3 或 10mg/kg 伊匹单抗治疗的晚期黑色素瘤患者的数据,进行了 TGD-OS 分析。混合模型使用三个亚群(无生长、中间和快速)描述 TGD 特征。TGD 模型显示出阳性的暴露/剂量反应(即,与 3mg/kg 剂量相比,10mg/kg 伊匹单抗组中无/中间生长亚群的患者比例更高,肿瘤生长速度更低)。最后,基于混合 TGD 模型的肿瘤反应测量值与非混合模型相比,提供了更好的 OS 预测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/581e/6875707/8b641fa274eb/PSP4-8-825-g001.jpg

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