基于 DNA 超分子水凝胶的保护性 NK 细胞储库用于增强三阴性乳腺癌治疗
Protective NK Cell Reservoir Based on DNA Supramolecular Hydrogel for Enhanced Triple-Negative Breast Cancer Therapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:An Open-Source, Automated Tumor-Infiltrating Lymphocyte Algorithm for Prognosis in Triple-Negative Breast Cancer.
An Open-Source, Automated Tumor-Infiltrating Lymphocyte Algorithm for Prognosis in Triple-Negative Breast Cancer.
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神经网络驱动的细胞分类器所定义的 TIL 变量,在三阴性乳腺癌(TNBC)患者的多个独立验证队列中均为稳健且独立的预后因素。
TIL(肿瘤浸润淋巴细胞)评估已被认为对三阴性乳腺癌(TNBC)具有预后和预测价值,但其结果受观察者内及观察者间差异影响,阻碍了广泛应用。本研究建立基于机器学习的乳腺癌 TIL 评分方法,并在多个 TNBC 队列中验证其预后潜力。实验设计:使用 QuPath 开源软件,在苏木精-伊红(H&E)染色切片上建立神经网络分类器,以识别肿瘤细胞、淋巴细胞、成纤维细胞和“其他”细胞。分析分类器生成的 TIL 测量值,并构建 5 种不同 TIL 变量。回顾性收集 171 例 TNBC 作为发现队列,以确定机器读取的 TIL 变量与患者结局的最佳关联。验证阶段评估了 749 例 TNBC 患者,组成 4 个独立验证亚组。
5 种机器 TIL 变量均与结局显著相关(所有比较 P<0.01),但在验证队列中的表现存在细胞类型特异性差异。Cox 回归显示,在校正分期、年龄和组织学分级等临床病理因素后,5 种 TIL 变量均独立关联总生存期改善(所有分析 P<0.0003)。
神经网络细胞分类器定义的 TIL 变量稳健,且在多个独立 TNBC 验证队列中是独立预后因素。这些客观的开源 TIL 变量可免费下载,可在前瞻性研究中进一步评估其临床效用。
Although tumor-infiltrating lymphocytes (TIL) assessment has been acknowledged to have both prognostic and predictive importance in triple-negative breast cancer (TNBC), it is subject to inter and intraobserver variability that has prevented widespread adoption. Here we constructed a machine-learning based breast cancer TIL scoring approach and validated its prognostic potential in multiple TNBC cohorts. EXPERIMENTAL DESIGN: Using the QuPath open-source software, we built a neural-network classifier for tumor cells, lymphocytes, fibroblasts, and "other" cells on hematoxylin-eosin (H&E)-stained sections. We analyzed the classifier-derived TIL measurements with five unique constructed TIL variables. A retrospective collection of 171 TNBC cases was used as the discovery set to identify the optimal association of machine-read TIL variables with patient outcome. For validation, we evaluated a retrospective collection of 749 TNBC patients comprised of four independent validation subsets.
We found that all five machine TIL variables had significant prognostic association with outcomes ( P 0.01 for all comparisons) but showed cell-specific variation in validation sets. Cox regression analysis demonstrated that all five TIL variables were independently associated with improved overall survival after adjusting for clinicopathologic factors including stage, age, and histologic grade ( P 0.0003 for all analyses).
Neural net-driven cell classifier-defined TIL variables were robust and independent prognostic factors in several independent validation cohorts of TNBC patients. These objective, open-source TIL variables are freely available to download and can now be considered for testing in a prospective setting to assess clinical utility. See related commentary by Symmans, p. 5446 .
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