前列腺癌
医学
间质细胞
生物标志物
成纤维细胞活化蛋白
前列腺
组织微阵列
数字化病理学
前列腺切除术
病理
免疫组织化学
肿瘤科
癌症研究
癌症
PCA3系列
生化复发
生物标志物发现
基质
癌症生物标志物
活检
肿瘤异质性
组织病理学
疾病
内科学
免疫疗法
生物信息学
肿瘤微环境
临床意义
外科病理学
精密医学
作者
Jenni Säilä,Timo‐Pekka Lehto,Antti Rannikko,Olli Kallioniemi,Tuomas Mirtti,Teijo Pellinen
标识
DOI:10.1002/2056-4538.70068
摘要
Prostate cancer (PCa) lacks reliable and accurate tissue-based biomarkers to support prognostic stratification and clinical treatment decisions. Current diagnostic assessment, including Gleason grading, has limitations such as interobserver variability and insufficient granularity for disease aggressiveness. Fibroblast activation protein (FAP) and α-smooth muscle actin (αSMA) have emerged as putative stromal biomarkers, but their prognostic value in localised PCa has not been validated at scale. In this study, we developed a novel artificial intelligence (AI)-augmented image analysis pipeline tailored for dual-marker immunohistochemistry of FAP and αSMA, enabling automated, tissue compartment-specific quantification of biomarker expression. This deep learning model was trained and validated using digitised high-resolution whole-slide images of tissue microarrays from three prostatectomy cohorts, comprising 4,097 cores from 835 patients with comprehensive clinical follow-up data. The AI pipeline demonstrated high accuracy in detecting epithelial, stromal, and immune compartments, as well as in quantifying FAP and αSMA signals. We validated stromal FAP as a robust prognostic marker consistently associated with adverse clinical outcomes, including earlier biochemical recurrence, metastasis, and cancer-specific death. Epithelial FAP and stromal αSMA showed additional prognostic associations in selected analyses, particularly in MRI-visible tumours. Our findings reinforce the biological and clinical relevance of stromal FAP in the prostate tumour microenvironment. By enabling standardised and scalable biomarker quantification, our newly developed AI-assisted workflow advances the clinical utility of FAP and αSMA and demonstrates the power of integrating digital pathology with biomarker quantification. This study represents a critical step toward implementing stromal biomarkers in routine PCa diagnostics and underscores the potential of AI-enhanced histopathology in advancing precision oncology.
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