Department of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Xiangya Hospital, Central South University, Changsha, 410008, China; Institute of Clinical Pharmacology, Engineering Research Center for Applied Technology of Pharmacogenomics of Ministry of Education, Central South University, Changsha, 410078, China; Department of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, China; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, 410008, China.
Department of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Xiangya Hospital, Central South University, Changsha, 410008, China; Institute of Clinical Pharmacology, Engineering Research Center for Applied Technology of Pharmacogenomics of Ministry of Education, Central South University, Changsha, 410078, China; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, 410008, China.
Eur J Surg Oncol. 2023 Sep;49(9):106902. doi: 10.1016/j.ejso.2023.04.001. Epub 2023 Apr 13.
Despite the wide reportage of prognostic factors for glioblastoma (GBM), it is difficult to determine how these factors interact to affect patients' survival. To determine the combination of prognostic factors, we retrospectively analyzed the clinic data of 248 IDH wild-type GBM patients and built a novel prediction model. The survival variables of patients were identified via univariate and multivariate analyses. In addition, the score prediction models were constructed by combining classification and regression tree (CART) analysis with Cox regression analysis. Finally, the prediction model was internally validated using the bootstrap method. Patients were followed for a median of 34.4 (interquartile range, 26.1-46.0) months. Multivariate analysis identified gross total resection (GTR) (HR 0.50, 95% CI: 0.38-0.67), unopened ventricles (HR 0.75 [0.57-0.99]), and MGMT methylation (HR 0.56 [0.41-0.76]) as favorable independent prognostic factors for PFS. GTR (HR 0.67 [0.49-0.92]), unopened ventricles (HR 0.60 [0.44-0.82]), and MGMT methylation (HR 0.54 [0.38-0.76]) were favorable independent prognostic factors for OS. In the process of building the model, we incorporated GTR, ventricular opening, MGMT methylation status, and age. The model had six and five terminal nodules in PFS and OS respectively. We grouped terminal nodes with similar hazard ratios together to form three sub-groups with different PFS and OS (P < 0.001). After the internal verification of bootstrap method, the model had a good fitting and calibration. GTR, unopened ventricles, and MGMT methylation were independently associated with more satisfactory survival. The novel score prediction model which we construct can provide a prognostic reference for GBM.
尽管胶质母细胞瘤(GBM)的预后因素已有广泛报道,但很难确定这些因素如何相互作用影响患者的生存。为了确定预后因素的组合,我们回顾性分析了 248 例 IDH 野生型 GBM 患者的临床资料,并建立了一个新的预测模型。通过单因素和多因素分析确定患者的生存变量。此外,通过分类回归树(CART)分析与 Cox 回归分析相结合构建评分预测模型。最后,使用自举法对内部分验证预测模型。患者中位随访时间为 34.4 个月(四分位间距 26.1-46.0)。多因素分析确定肿瘤全切除(GTR)(HR 0.50,95%CI:0.38-0.67)、未打开脑室(HR 0.75 [0.57-0.99])和 MGMT 甲基化(HR 0.56 [0.41-0.76])是 PFS 的有利独立预后因素。GTR(HR 0.67 [0.49-0.92])、未打开脑室(HR 0.60 [0.44-0.82])和 MGMT 甲基化(HR 0.54 [0.38-0.76])是 OS 的有利独立预后因素。在构建模型的过程中,我们纳入了 GTR、脑室开放、MGMT 甲基化状态和年龄。该模型在 PFS 和 OS 中分别有 6 个和 5 个末端节点。我们将具有相似风险比的末端节点分组在一起,形成具有不同 PFS 和 OS 的三个亚组(P<0.001)。通过自举法的内部验证,该模型具有良好的拟合度和校准度。GTR、未打开脑室和 MGMT 甲基化与更满意的生存独立相关。我们构建的新评分预测模型可为 GBM 提供预后参考。