Pane Katia, Mirabelli Peppino, Coppola Luigi, Illiano Ester, Salvatore Marco, Franzese Monica
IRCCS SDN, Naples, Italy.
Andrological and Urogynecological Clinic, Santa Maria Terni Hospital, University of Perugia, Terni, Italy.
Front Chem. 2020 Jul 31;8:600. doi: 10.3389/fchem.2020.00600. eCollection 2020.
About 70% of bladder cancers (BCs) are diagnosed as non-muscle-invasive BCs (NMIBCs), while the remaining are muscle-invasive BCs (MIBCs). The European Association of Urology (EAU) guidelines stratify NMIBCs into low, intermediate, and high risk for treatment options. Low-risk NMIBCs undergo only the transurethral resection of the bladder (TURB), whereas for intermediate-risk and high-risk NMIBCs, the transurethral resection of the bladder (TURB) with or without (BCG) immune or chemotherapy is the standard treatment. A minority of NMIBCs show unfavorable prognosis. High-risk NMIBCs have a high rate of disease recurrence and/or progression to muscle-invasive tumor and BCG treatment failure. The heterogeneous nature of NMIBCs poses challenges for clinical decision-making. In 2020, the EAU made some changes to NMIBCs BCG failure definitions and treatment options, highlighting the need for reliable molecular markers for improving the predictive accuracy of currently available risk tables. Nowadays, next-generation sequencing (NGS) has revolutionized the study of cancer biology, providing diagnostic, prognostic, and therapy response biomarkers in support of precision medicine. Integration of NGS with other cutting-edge technologies might help to decipher also bladder tumor surrounding aspects such as immune system, stromal component, microbiome, and urobiome; altogether, this might impact the clinical outcomes of NMBICs especially in the BCG responsiveness. This review focuses on NMIBCs with unfavorable prognoses, providing molecular prognostic factors from tumor immune and stromal cells, and the perspective of urobiome and microbiome profiling on therapy response. We provide information on the cornerstone of immunotherapy and new promising bladder-preserving treatments and ongoing clinical trials for BCG-unresponsive NMIBCs.
约70%的膀胱癌(BC)被诊断为非肌层浸润性膀胱癌(NMIBC),其余为肌层浸润性膀胱癌(MIBC)。欧洲泌尿外科学会(EAU)指南根据治疗方案将NMIBC分为低、中、高风险。低风险NMIBC仅接受经尿道膀胱肿瘤切除术(TURB),而对于中风险和高风险NMIBC,经尿道膀胱肿瘤切除术(TURB)联合或不联合卡介苗(BCG)免疫治疗或化疗是标准治疗方法。少数NMIBC预后不良。高风险NMIBC疾病复发和/或进展为肌层浸润性肿瘤以及BCG治疗失败的发生率较高。NMIBC的异质性给临床决策带来了挑战。2020年,EAU对NMIBC的BCG失败定义和治疗方案进行了一些更改,强调需要可靠的分子标志物来提高现有风险表的预测准确性。如今,新一代测序(NGS)彻底改变了癌症生物学研究,提供了诊断、预后和治疗反应生物标志物以支持精准医学。将NGS与其他前沿技术相结合可能有助于解读膀胱肿瘤周围的其他方面,如免疫系统、基质成分、微生物群和尿微生物群;总体而言,这可能会影响NMBIC的临床结局,尤其是在BCG反应性方面。本综述重点关注预后不良的NMIBC,提供肿瘤免疫和基质细胞的分子预后因素,以及尿微生物群和微生物群分析对治疗反应的前景。我们提供免疫治疗的基石、新的有前景的保膀胱治疗方法以及针对BCG无反应性NMIBC的正在进行的临床试验的信息。