研究概要
扩展后的LundTax系统为个体肿瘤活检提供了全面的分子画像。
中文摘要
膀胱癌是一种异质性恶性肿瘤,临床结局多样,仅靠传统病理评估不足以捕捉其 underlying biology。基因表达谱可将肿瘤分层为具有预后和预测潜力的分子亚型,但转录组分类的可靠性及其临床实用性仍有待确立。转化/观察性 UROSCANSEQ 研究(ISRCTN15459149)在临床环境中前瞻性评估基于 RNA 的 Lund Taxonomy(LundTax)分子亚型分类。在 2018 年至 2022 年间连续收集的 784 份活检中,90% 的活检 RNA 测序成功,涵盖 662 例膀胱癌患者,分期分布为 48% Ta、27% T1、24% ≥T2 和 1% CIS。我们证明,应用于单个样本的 LundTax 亚型分类算法能够准确识别具有特征性基因和蛋白表达模式的癌细胞表型,且对 RNA 质量、数据预处理策略和批次效应具有稳健性,支持其在非肌层浸润性和肌层浸润性疾病中的临床可行性。我们进一步扩展了 LundTax 框架,纳入反映肿瘤分级、增殖和进展风险的单样本分子风险评分,以及肿瘤微环境特征。风险评分以及活检中总体免疫和基质含量均与非浸润性疾病临床进展风险增加显著相关。然而,在对肿瘤微环境相对细胞组成的单独分析中,只有NK 细胞比例仍然显著。总之,扩展后的LundTax系统为个体肿瘤活检提供了全面的分子画像。通过明确区分癌细胞内在表型、预后指数和微环境信号,该框架最大限度地减少了生物学混杂,并为未来评估临床结局和治疗反应的研究奠定了坚实基础。
展开英文摘要原文
Bladder cancer is a heterogeneous malignancy with diverse clinical outcomes, and conventional pathological assessment alone is insufficient to capture its underlying biology. Gene expression profiling can stratify tumors into molecular subtypes with prognostic and predictive potential, but the reliability of transcriptomic classification and its clinical utility remains to be established. The translational/observational UROSCANSEQ study (ISRCTN15459149) prospectively evaluates RNA-based Lund Taxonomy (LundTax) molecular subtype classification in a clinical setting. Among 784 consecutive biopsies collected between 2018 and 2022, RNA sequencing was successful for 90% of all biopsies, encompassing 662 bladder cancer patients with a stage distribution of 48% Ta, 27% T1, 24% ≥T2, and 1% CIS. We demonstrate that the LundTax subtype classification algorithm, applied to individual samples, accurately identifies cancer cell phenotypes with characteristic gene and protein expression patterns in a manner robust to RNA quality, data preprocessing strategies, and batch effects, supporting its clinical feasibility across both non-muscle-invasive and muscle-invasive disease. We further extend the LundTax framework by incorporating single-sample molecular risk scores reflecting tumor grade, proliferation, and progression risk, as well as tumor microenvironment signatures. Both risk scores and overall immune and stromal content in biopsies were significantly associated with an increased risk of clinical progression in noninvasive disease. In a separate analysis of the relative cellular composition of the tumor microenvironment, however, only the fraction of natural killer cells remained significant. Together, the expanded LundTax system provides a comprehensive molecular portrait of individual tumor biopsies. By explicitly separating cancer cell-intrinsic phenotypes, prognostic indexes, and microenvironmental signals, the framework minimizes biological confounding and establishes a strong foundation for future studies evaluating clinical outcomes and treatment responses.
论文信息
- 作者
- Eriksson P、Cotillas EA、Mattsson CA、Zadoroznyj A、Bernardo C、Sjödahl G、Edsjö A、Heidenblad M
- 单位
- Division of Oncology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden. Electronic address: pontus.eriksson@med.lu.se.Sweden
- 文献类型
- 非美国政府资助研究
- 期刊
- Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2026 Jun