Clinical Pharmacology & Safety Sciences, AstraZeneca, Cambridge, UK.
Clinical Pharmacology & Safety Sciences, AstraZeneca, Gaithersburg, Maryland, USA.
CPT Pharmacometrics Syst Pharmacol. 2021 Mar;10(3):230-240. doi: 10.1002/psp4.12594. Epub 2021 Feb 13.
We developed and evaluated a method for making early predictions of best overall response (BOR) and overall survival at 6 months (OS6) in patients with cancer treated with immunotherapy. This method combines machine learning with modeling of longitudinal tumor size data. We applied our method to data from durvalumab-exposed patients with recurrent/metastatic head and neck cancer. A fivefold cross-validation was used for model selection. Independent trial data, with various degrees of data truncation, were used for model validation. Mean classification error rates (90% confidence intervals [CIs]) from cross-validation were 5.99% (90% CI 2.98%-7.50%) for BOR and 19.8% (90% CI 15.8%-39.3%) for OS6. During model validation, the area under the receiver operating characteristic curves was preserved for BOR (0.97, 0.97, and 0.94) and OS6 (0.85, 0.84, and 0.82) at 24, 18, and 12 weeks, respectively. These results suggest our method predicts trial outcomes accurately from early data and could be used to aid drug development.
我们开发并评估了一种方法,用于对接受免疫治疗的癌症患者进行早期预测最佳总体反应(BOR)和 6 个月总生存(OS6)。该方法将机器学习与纵向肿瘤大小数据建模相结合。我们将我们的方法应用于接受度伐单抗治疗的复发性/转移性头颈部癌症患者的数据中。采用五重交叉验证进行模型选择。使用具有不同程度数据截断的独立试验数据进行模型验证。来自交叉验证的平均分类错误率(90%置信区间[CI])分别为 BOR 的 5.99%(90%CI 2.98%-7.50%)和 OS6 的 19.8%(90%CI 15.8%-39.3%)。在模型验证过程中,BOR 的接收者操作特征曲线下面积保持不变(0.97、0.97 和 0.94),OS6 分别为 24、18 和 12 周(0.85、0.84 和 0.82)。这些结果表明,我们的方法可以从早期数据中准确预测试验结果,并可用于辅助药物开发。