CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Development and validation of a gradient boosting machine-based model for predicting tumor-infiltrating lymphocyte proportions in breast cancer.
Development and validation of a gradient boosting machine-based model for predicting tumor-infiltrating lymphocyte proportions in breast cancer.
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基于胶质母细胞瘤的多维模型可可靠预测乳腺癌患者的 TIL 水平,支持预后评估并指导个体化治疗策略。
构建并验证用于评估乳腺癌(BC)患者TIL(肿瘤浸润淋巴细胞)水平的多维模型。
本回顾性研究纳入 2021 年 1 月至 2024 年 12 月在广西医科大学第一附属医院就诊、经 MRI 和手术病理确诊的 318 例 BC 患者及 318 个病灶。患者随机分为训练集(n = 228)和验证集(n = 90),并依据免疫表型评估分为 TIL 低水平组和高水平组。采用多变量 Logistic 回归确定 TIL 水平的独立预测因素,并构建梯度提升机(GBM)和 Logistic 回归模型。通过 ROC 曲线、校准曲线和决策曲线分析(DCA)评估模型表现。另以 2025 年 1 月至 5 月收治的 120 例 BC 患者作为外部验证队列,验证 GBM 模型的预测准确性。
Ki-67 水平、内部强化模式、多灶性、表观扩散系数(ADC)值及中性粒细胞/淋巴细胞比值(NLR)被确定为高 TIL 水平的独立预测因素。训练集中 GBM 模型表现优于 Logistic 回归(AUC:0.859 对 0.724;P = 0.014)。两种模型的校准曲线均显示预测概率与观察概率吻合良好。DCA 显示 GBM 模型临床效用更高。外部验证中 GBM 模型 AUC 为 0.784,校准曲线和 DCA 进一步证实其校准良好且具临床适用性。
基于 GBM 的多维模型可可靠预测 BC 患者 TIL 水平,有助于预后评估并指导个体化治疗策略。
To construct and validate a multidimensional model for evaluating tumor-infiltrating lymphocyte (TIL) levels in breast cancer (BC) patients.
This retrospective study included 318 BC patients with 318 lesions confirmed by MRI and surgical pathology in the First Affiliated Hospital of Guangxi Medical University from January 2021 to December 2024. The patients were randomly split into a training set (n=228) and a validation (n=90) set, and further divided into low and high TIL groups based on immunophenotype assessment. Multivariate Logistic regression was used to identify independent predictors of TILs levels. A gradient boosting machine (GBM) model and a Logistic regression model were built. Model performance was assessed using receiver operating characteristic (ROC) curves, calibration curves, and decision curve analysis (DCA). An external validation cohort of 120 BC patients admitted between January 2025 and May 2025 was used to verify the predictive accuracy of the GBM model. Results Ki-67 level, internal enhancement pattern, multifocality, apparent diffusion coefficient (ADC) value, and neutrophil-to-lymphocyte ratio (NLR) were identified as independent predictors of high TIL levels. The GBM model demonstrated superior performance compared to the Logistic regression in the training set (AUC: 0.859 vs 0.724; P=0.014). Calibration curves indicated good agreement between predicted and observed probabilities in both models. DCA showed that the GBM model provided higher clinical utility. External validation yielded an AUC of 0.784 for the GBM model, with the calibration curve and DCA further confirming the model's good calibration and clinical applicability.
The GBM-based multidimensional model reliably predicts TIL levels in BC patients, supporting prognosis evaluation and guiding personalized treatment strategies.
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