一种用于克服非小细胞肺癌治疗中抗原异质性的多靶向 CAR-T 细胞平台
A Multi-Targeting Chimeric Antigen Receptor-T Cell Platform to Overcome Antigen Heterogeneity in the Treatment of Non-Small Cell Lung Cancer.
这些发现支持采用多靶点CAR-T 策略来应对NSCLC及可能其他实体瘤中的抗原异质性。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Feature Engineering Assessment of Tumor Infiltrating Lymphocytes in Lung Adenocarcinoma.
Feature Engineering Assessment of Tumor Infiltrating Lymphocytes in Lung Adenocarcinoma.
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TIL(肿瘤浸润淋巴细胞)正逐渐成为免疫治疗的预后标志物。目前,TIL由病理学家在肿瘤组织的苏木精-伊红(H&E)染色切片上进行评估。这种方法耗时,且存在观察者间变异。本研究旨在提出一种基于机器学习的算法,称为特征工程TIL评估(FTA),利用腺癌元数据(即病史、临床和病理数据)进行TIL的自动评估。该算法为弹性网络,通过贝叶斯优化进行调优,并通过留一受试者交叉验证进行验证。获得的系数用于特征排序。结果证实了FTA的良好性能,总体平均绝对误差为2.1%,一致性相关系数为0.71,Bland-Altman图中的差异为-0.001。获得的特征排序揭示了性别的关键作用,这与临床文献一致。总之,FTA是首个不依赖图像的自动TIL评估方法,有潜力解决观察者间变异和经典方法耗时的问题。
Tumor-Infiltrating Lymphocytes (TIL) are emerging as immunotherapy prognostic markers. Currently, TIL are assessed on hematoxylin and eosin (H&E)-stained slides of tumor tissue by pathologists. This approach is time-consuming, and subjected to inter-observer variability. The aim of this study is to propose a machine learning-based algorithm, called Feature Engineering TIL Assessment (FTA), for the automatic TIL assessment by using adenocarcinoma metadata (i. e. , anamnestic, clinical and pathological data).
The algorithm is an Elastic Net, tuned by Bayesian Optimization and validated by Leave-One-Subject-Out cross validation. Obtained coefficients were used for feature ranking. Results confirms the goodness of performance of FTA, with an overall Mean Absolute Error of 2. 1%, Concordance Correlation Coefficient equal to 0. 71 and difference in the Bland- Altman plot equal to -0. 001. The obtained feature ranking revealed the key role of gender, as confirmed by the clinical literature.
In conclusion, FTA is the first image-independent automatic TIL assessment procedure, having the potential to address challenges associated with inter-observer variability and the time-consuming nature of classical procedures.
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