NHC Key Laboratory of Glycoconjugate Research, Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Department of Urology, Zhongshan Hospital, Fudan University, Shanghai, China.
Br J Cancer. 2024 Mar;130(5):852-860. doi: 10.1038/s41416-023-02572-9. Epub 2024 Jan 11.
Cyclin-dependent kinase 6 (CDK6) was proved to be an important regulator in the progression of cell cycle and has been a promising therapeutic target in cancer treatment. However, the clinical significance of CDK6 in muscle-invasive bladder cancer (MIBC) remains obscure. Herein, we attempt to explore the clinical relevance of CDK6 and assess the feasibility of the integrative model to predict immune checkpoint blockade (ICB) response.
This study enrolled 933 patients with muscle-invasive bladder cancer (MIBC) from Zhongshan Hospital (ZSHS), The Cancer Genome Atlas (TCGA), Chemo, IMvigor210 and UC-GENOME cohorts. Kaplan-Meier survival and Cox regression analyses were performed to assess clinical outcomes based on CDK6 expression.
High CDK6 expression conferred poor prognosis and superior response to platinum-based chemotherapy but inferior response to ICB in MIBC. Furthermore, the integrative model named response score based on CDK6, PD-L1 and TMB could better predict the response to ICB and chemotherapy. Patients with higher response scores were characterised by inflamed immune microenvironment and genomic instability.
CDK6 expression was correlated with prognosis and therapy response in MIBC. Integration of CDK6, PD-L1 and TMB could better identify patients who were most likely to benefit from ICB and chemotherapy.
细胞周期蛋白依赖性激酶 6(CDK6)被证明是细胞周期进展的重要调节因子,已成为癌症治疗中有前途的治疗靶点。然而,CDK6 在肌层浸润性膀胱癌(MIBC)中的临床意义仍不清楚。在此,我们试图探讨 CDK6 的临床相关性,并评估整合模型预测免疫检查点阻断(ICB)反应的可行性。
本研究纳入了来自中山医院(ZSHS)、癌症基因组图谱(TCGA)、化疗、IMvigor210 和 UC-GENOME 队列的 933 例肌层浸润性膀胱癌(MIBC)患者。基于 CDK6 表达,通过 Kaplan-Meier 生存和 Cox 回归分析评估临床结局。
高 CDK6 表达预示着 MIBC 患者预后不良,对铂类化疗反应良好,但对 ICB 反应较差。此外,命名为基于 CDK6、PD-L1 和 TMB 的反应评分的整合模型,可更好地预测 ICB 和化疗的反应。具有更高反应评分的患者具有炎症免疫微环境和基因组不稳定性的特征。
CDK6 表达与 MIBC 的预后和治疗反应相关。CDK6、PD-L1 和 TMB 的整合可以更好地识别最有可能从 ICB 和化疗中获益的患者。