PO.CL01.14 · 临床研究

尿路上皮癌新辅助atezolizumab治疗后肿瘤微环境的空间与转录组重塑:来自ABACUS研究的见解

Spatial and transcriptomic remodeling of the tumor microenvironment following neoadjuvant atezolizumab in urothelial carcinoma: Insights from the ABACUS Study

海报缩略图:尿路上皮癌新辅助atezolizumab治疗后肿瘤微环境的空间与转录组重塑:来自ABACUS研究的见解
编号 6668 展板 10 时间 4/21 02:00–05:00 区域 Section 48 主讲 Robbin Nameki, PhD
分会场 Spatial Proteomics and Transcriptomics 3
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作者与单位 Authors & Affiliations

Robbin Nameki1, Jennifer Kinong1, Chao-Hui Huang1, Michelle Saul1, Aakash Sur1, Mehmet Tekman1, Alexander Trageser1, Wenjing Yang1, Daniel Chawla1, Greg Szeto1, Arne Schmidt2, Alberto Megina Gonzalo2, Srishti Munjal Mehta2, Nina Kozar-Gillan2, Rosemarie Krupar2, Sophie Laturnus2, Cornelius Bohm2, Marija Pezer2, Gloria H.Y. Lin1, Diane Fernandez1, Keith Ching1, Jadwiga R. Bienkowska1, Thomas Powles3, Craig B. Davis1

1Pfizer, Inc., San Diego, CA,2Aignostics, Berlin, Germany,3Experimental Cancer Medicine Centre, Barts Cancer Institute, London, United Kingdom

摘要 Abstract

中文摘要
ABACUS研究是一项评估可手术尿路上皮癌新辅助atezolizumab治疗的单臂II期试验。分析了配对的基线和治疗后肿瘤标本,以识别与治疗应答相关的生物标志物。初步的批量转录组学和免疫组织化学分析提示,免疫激活、组织重塑与耐药通路之间的联系与临床结局相关。为进一步在高分辨率下表征空间和表型变化,对配对样本进行了人工智能辅助的苏木精-伊红切片数字图像分析和Visium空间转录组学。治疗后标本显示肿瘤微环境的广泛重塑,伴随显著的免疫浸润、基质扩张和内皮-肿瘤邻近性的改变。此类改变与疾病稳定和复发之间不同的临床结局相关。这些发现表明,atezolizumab通过促进免疫浸润和重塑基质结构重塑了肿瘤微环境;然而,尽管免疫扩张,强健的肿瘤和内皮活性可能维持免疫排斥并驱动耐药。此处识别的空间和表型生物标志物可为免疫检查点抑制剂难治性尿路上皮癌的合理联合策略提供依据。
查看英文原文 English abstract
The ABACUS study was a single-arm, phase II trial evaluating neoadjuvant atezolizumab in operable urothelial carcinoma. Paired baseline and post-treatment tumor specimens were analyzed to identify biomarkers associated with treatment response. Initial bulk transcriptomic and immunohistochemistry analyses suggested links between immune activation, tissue remodeling and resistance pathways were associated with clinical outcome. To further characterize spatial and phenotypic changes at high resolution, artificial intelligence-assisted digital image analysis of hematoxylin & eosin sections and Visium spatial transcriptomics were performed on paired samples. Post-treatment specimens showed extensive remodeling of the tumor microenvironment with marked immune infiltration, stromal expansion, and altered endothelial-tumor proximity. Such alterations were associated with distinct clinical outcomes between stable disease and relapse. These findings indicate that atezolizumab reshapes the tumor microenvironment by enabling immune infiltration and remodeling stromal architecture; however, robust tumor and endothelial activity may sustain immune exclusion and drive resistance despite immune expansion. Spatial and phenotypic biomarkers identified here may inform rational combination strategies for immune checkpoint inhibitor-refractory urothelial carcinoma.
利益披露 Disclosure
R. Nameki, Pfizer, Inc. Employment. J. Kinong, Pfizer Employment. C. Huang, Pfizer Employment. M. Saul, Pfizer Employment. A. Sur, Pfizer Employment. M. Tekman, Pfizer Employment. A. Trageser, Pfizer Employment. W. Yang, Pfizer Employment. D. Chawla, Pfizer Employment. G. Szeto, Pfizer Employment. A. Schmidt, Aignostics Employment. A. M. Gonzalo, Aignostics Employment. S. M. Mehta, Aignostics Employment. N. Kozar-Gillan, Aignostics Employment. R. Krupar, Aignostics Employment. S. Laturnus, Aignostics Employment. C. Bohm, Aignostics Employment. M. Pezer, Aignostics Employment. G. H. Lin, Pfizer Employment. D. Fernandez, Pfizer Employment. K. Ching, Pfizer Employment. J. R. Bienkowska, Pfizer Employment. T. Powles, Astellas Pharma Other, Consulting. AstraZeneca Other, Consulting. Bristol Myers Squibb Consulting. Eisai Consulting. Exelixis Other, Consulting. Incyte Consulting. Ipsen Consulting. Johnson & Johnson Other, Consulting. Merck Other, Consulting. MSD Other, Consulting. Novartis Other, Consulting. Pfizer Consulting. Roche Consulting. C. B. Davis, Pfizer Employment.

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