Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta University, 1410 Laney Walker Blvd., Augusta, GA 30912, USA.
Int J Mol Sci. 2024 Sep 13;25(18):9899. doi: 10.3390/ijms25189899.
The clinical outcome of patients with muscle-invasive bladder cancer (MIBC) is poor despite the approval of neoadjuvant chemotherapy or immunotherapy to improve overall survival after cystectomy. MIBC subtypes, immune, transcriptome, metabolomic signatures, and mutation burden have the potential to predict treatment response but none have been incorporated into clinical practice, as tumor heterogeneity and lineage plasticity influence their efficacy. Using the PRISMA statement, we conducted a systematic review of the literature, involving 135 studies published within the last five years, to identify studies reporting on the prognostic value of protein-based biomarkers for response to neoadjuvant therapy in patients with MIBC. The studies were grouped based on biomarkers related to molecular subtypes, cancer stem cell, actin-cytoskeleton, epithelial-mesenchymal transition, apoptosis, and tumor-infiltrating immune cells. These studies show the potential of protein-based biomarkers, especially in the spatial context, to reduce the influence of tumor heterogeneity on a biomarker's prognostic capability. Nevertheless, currently, there is little consensus on the methodology, reagents, and the scoring systems to allow reliable assessment of the biomarkers of interest. Furthermore, the small sample size of several studies necessitates the validation of potential prognostic biomarkers in larger multicenter cohorts before their use for individualizing neoadjuvant therapy regimens for patients with MIBC.
尽管新辅助化疗或免疫疗法已被批准用于改善膀胱癌患者(MIBC)的术后总生存率,但 MIBC 患者的临床预后仍较差。MIBC 亚型、免疫、转录组、代谢组学特征和突变负担具有预测治疗反应的潜力,但尚未纳入临床实践,因为肿瘤异质性和谱系可塑性影响其疗效。我们根据 PRISMA 声明,对过去五年内发表的 135 项研究进行了系统综述,以确定报告 MIBC 患者新辅助治疗反应的基于蛋白质的生物标志物预后价值的研究。这些研究根据与分子亚型、癌症干细胞、肌动蛋白细胞骨架、上皮-间充质转化、细胞凋亡和肿瘤浸润免疫细胞相关的生物标志物进行分组。这些研究表明,基于蛋白质的生物标志物(尤其是在空间背景下)具有降低肿瘤异质性对生物标志物预后能力影响的潜力。然而,目前对于方法学、试剂和评分系统的共识很少,无法对有前途的生物标志物进行可靠评估。此外,由于几个研究的样本量较小,因此在将潜在的预后生物标志物用于 MIBC 患者的个体化新辅助治疗方案之前,需要在更大的多中心队列中对其进行验证。