Hu Jiao, Yan Luzhe, Liu Jinhui, Chen Minfeng, Liu Peihua, Deng Dingshan, Zhang Chaobin, He Yunbo, Fan Benyi, Li Huihuang, Gong Guanghui, Xiao Jiatong, Wang Ruizhe, Guan Xiao, Tong Shiyu, Li Yangle, Li Nannan, Tang Zhiwang, Zhang Teng, Li Hao, Huang Bin, Gao Ning, He Wei, Cai Zhiyong, Liu Yifan, Liu Zefu, Gan Yu, Cui Yu, Dai Yuanqing, Cai Yi, Nie Zhenyu, Ou Zhenyu, Chen Jinbo, Zu Xiongbing
Department of Urology, Xiangya Hospital Central South University Changsha China.
National Clinical Research Center for Geriatric Disorders, Xiangya Hospital Central South University Changsha China.
Imeta. 2025 Apr 14;4(3):e70033. doi: 10.1002/imt2.70033. eCollection 2025 Jun.
In this study, 102 cisplatin-ineligible patients with muscle-invasive bladder cancer (MIBC) who received neoadjuvant RC48-ADC combined with immunotherapy were included. We evaluated the pathological responses and explored multiple clinical characteristics to identify independent predictive indicators of the efficacy. The results showed that neoadjuvant RC48-ADC combined with immunotherapy had promising efficacy. Furthermore, we collected 11 MIBC samples and performed single-cell RNA sequencing. All BLCA epithelial cells were identified as four subclusters. We conducted differential gene expression/functional enrichment analysis, cell proportion analysis, cell cycle analysis, CNV analysis, and pseudotemporal analysis on all tumor cells to evaluate potential efficacy-predictive biomarkers and the evolutionary patterns of tumor cells during neoadjuvant treatment. The results indicated that the combined detection of HER2 and HSPA1A expression in C3 subcluster based on single-cell RNA sequencing is a potential strategy for predicting efficacy. In addition, C3 plays a dominant role in the emergence of drug-resistance during the evolution of BLCA epithelial cells.
在本研究中,纳入了102例不符合顺铂治疗条件的肌肉浸润性膀胱癌(MIBC)患者,这些患者接受了新辅助RC48-抗体药物偶联物(ADC)联合免疫治疗。我们评估了病理反应,并探索了多种临床特征以确定疗效的独立预测指标。结果表明,新辅助RC48-ADC联合免疫治疗具有良好的疗效。此外,我们收集了11例MIBC样本并进行了单细胞RNA测序。所有膀胱尿路上皮癌(BLCA)上皮细胞被鉴定为四个亚群。我们对所有肿瘤细胞进行了差异基因表达/功能富集分析、细胞比例分析、细胞周期分析、拷贝数变异(CNV)分析和拟时序分析,以评估潜在的疗效预测生物标志物以及新辅助治疗期间肿瘤细胞的进化模式。结果表明,基于单细胞RNA测序联合检测C3亚群中HER2和热休克蛋白家族A成员1A(HSPA1A)的表达是一种预测疗效的潜在策略。此外,C3在BLCA上皮细胞进化过程中耐药性的出现中起主导作用。