The role of TERT C228T and KDM6A alterations and TME in NMIBC treated with BCG

• Published in: NPJ precision oncology Vol. 8; no. 1; pp. 216 - 13
• Main Authors: Xia, Qi-Dong, Sun, Jian-Xuan, Yao, Zhi-Peng, Lu, Jun-Lin, Liu, Chen-Qian, Xu, Jin-Zhou, An, Ye, Xu, Meng-Yao, Zhang, Si-Han, Zhong, Xing-Yu, Zeng, Na, Ma, Si-Yang, He, Hao-Dong, Hu, Heng-Long, Hu, Jia, Lu, Yi, Li, Bing, Chen, Yao-Bing, Liu, Zheng, Wang, Shao-Gang
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.10.2024; Nature Publishing Group; Nature Portfolio
• Subjects: 631/67/589/1336; 631/67/69; Biomarkers; Bladder cancer; Cancer Research; Chemotherapy; Gene Therapy; Hospitals; Human Genetics; Internal Medicine; Medicine; Medicine & Public Health; Mutation; Oncology; Urology
• ISSN: 2397-768X; 2397-768X
• DOI: 10.1038/s41698-024-00725-4

We aimed to investigate the genomic and tumor microenvironmental (TME) profiles in non-muscle invasive bladder cancer (NMIBC) and explore potential predictive markers for Bacillus Calmette–Guérin (BCG) treatment response in high-risk NMIBC patients (according to European Association of Urology (EAU) risk stratification). 40 patients with high-risk NMIBC (cTis-T1N0M0) who underwent en bloc resection followed by BCG instillation were retrospectively enrolled. Surgical samples were subjected to Next Generation Sequencing (NGS) and multiplex immunofluorescence (mIF) assay. Genomic profiling revealed high prevalences of alterations in TERT (55%), KDM6A (32.5%), FGFR3 (30%), PIK3CA (30%), TP53 (27.5%) and ARID1A (20%). TME analysis showed different proportions of macrophages, NK cells, T cells subsets in tumoral and stromal compartment. Multivariate analysis identified TERT C228T and alteration in KDM6A as two independent factors associated with inferior RFS. The study comprehensively depicted the genomic and TME profiles in NMIBC and identified potential predictive biomarkers for BCG treatment.