Cytel, Toronto, Ontario, Canada.
University of Toronto, Toronto, Ontario, Canada.
JCO Clin Cancer Inform. 2021 Mar;5:326-337. doi: 10.1200/CCI.20.00107.
To address the need for more accurate risk stratification models for cancer immuno-oncology, this study aimed to develop a machine-learned Bayesian network model (BNM) for predicting outcomes in patients with metastatic renal cell carcinoma (mRCC) being treated with immunotherapy.
Patient-level data from the randomized, phase III CheckMate 025 clinical trial comparing nivolumab with everolimus for second-line treatment in patients with mRCC were used to develop the BNM. Outcomes of interest were overall survival (OS), all-cause adverse events, and treatment-related adverse events (TRAE) over 36 months after treatment initiation. External validation of the model's predictions for OS was conducted using data from select centers from the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC).
Areas under the receiver operating characteristic curve (AUCs) for BNM-based classification of OS using baseline data were 0.74, 0.71, and 0.68 over months 12, 24, and 36, respectively. AUC for OS at 12 months increased to 0.86 when treatment response and progression status in year 1 were included as predictors; progression and response at 12 months were highly prognostic of all outcomes over the 36-month period. AUCs for adverse events and treatment-related adverse events were approximately 0.6 at 12 months but increased to approximately 0.7 by 36 months. Sensitivity analysis comparing the BNM with machine learning classifiers showed comparable performance. Test AUC on IMDC data for 12-month OS was 0.71 despite several variable imbalances. Notably, the BNM outperformed the IMDC risk score alone.
The validated BNM performed well at prediction using baseline data, particularly with the inclusion of response and progression at 12 months. Additionally, the results suggest that 12 months of follow-up data alone may be sufficient to inform long-term survival projections in patients with mRCC.
为了针对癌症免疫肿瘤学更准确的风险分层模型的需求,本研究旨在开发一种用于预测接受免疫治疗的转移性肾细胞癌(mRCC)患者结局的机器学习贝叶斯网络模型(BNM)。
使用来自随机、III 期 CheckMate 025 临床试验的患者水平数据,该试验比较了纳武单抗与依维莫司在 mRCC 二线治疗中的疗效,用于开发 BNM。感兴趣的结局包括总生存(OS)、全因不良事件和治疗相关不良事件(TRAE),随访时间为治疗开始后 36 个月。使用国际转移性肾细胞癌数据库联盟(IMDC)选定中心的数据对模型的 OS 预测进行外部验证。
基于基线数据的 BNM 分类的 OS 曲线下面积(AUC)分别为 12、24 和 36 个月时的 0.74、0.71 和 0.68。当将 1 年时的治疗反应和进展状态作为预测因子纳入时,12 个月时的 OS AUC 增加到 0.86;12 个月时的进展和反应对 36 个月内的所有结局均具有高度预后价值。12 个月时不良事件和治疗相关不良事件的 AUC 约为 0.6,但到 36 个月时增加到约 0.7。与机器学习分类器比较的敏感性分析显示,性能相当。尽管存在多个变量不平衡,但是在 IMDC 数据中,12 个月 OS 的测试 AUC 为 0.71。值得注意的是,BNM 的表现优于单独的 IMDC 风险评分。
验证后的 BNM 在使用基线数据进行预测时表现良好,尤其是在纳入 12 个月时的反应和进展情况时。此外,结果表明,单独 12 个月的随访数据可能足以提供 mRCC 患者长期生存预测。