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治疗尿路上皮癌的当前及新出现的策略

Current and Emerging Strategies to Treat Urothelial Carcinoma.

作者信息

Rani Berkha, Ignatz-Hoover James J, Rana Priyanka S, Driscoll James J

机构信息

Case Comprehensive Cancer Center, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.

Division of Hematology & Oncology, Department of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.

出版信息

Cancers (Basel). 2023 Oct 8;15(19):4886. doi: 10.3390/cancers15194886.

Abstract

Urothelial cell carcinoma (UCC, bladder cancer, BC) remains a difficult-to-treat malignancy with a rising incidence worldwide. In the U.S., UCC is the sixth most incident neoplasm and ~90% of diagnoses are made in those >55 years of age; it is ~four times more commonly observed in men than women. The most important risk factor for developing BC is tobacco smoking, which accounts for ~50% of cases, followed by occupational exposure to aromatic amines and ionizing radiation. The standard of care for advanced UCC includes platinum-based chemotherapy and programmed cell death (PD-1) or programmed cell death ligand 1 (PD-L1) inhibitors, administered as frontline, second-line, or maintenance therapy. UCC remains generally incurable and is associated with intrinsic and acquired drug and immune resistance. UCC is lethal in the metastatic state and characterized by genomic instability, high PD-L1 expression, DNA damage-response mutations, and a high tumor mutational burden. Although immune checkpoint inhibitors (ICIs) achieve long-term durable responses in other cancers, their ability to achieve similar results with metastatic UCC (mUCC) is not as well-defined. Here, we discuss therapies to improve UCC management and how comprehensive tumor profiling can identify actionable biomarkers and eventually fulfill the promise of precision medicine for UCC patients.

摘要

尿路上皮癌(UCC,膀胱癌,BC)仍然是一种难以治疗的恶性肿瘤,在全球范围内发病率呈上升趋势。在美国,UCC是第六大常见肿瘤,约90%的诊断病例发生在55岁以上人群中;男性的发病率约为女性的四倍。患膀胱癌最重要的风险因素是吸烟,约占病例的50%,其次是职业接触芳香胺和电离辐射。晚期UCC的标准治疗包括铂类化疗以及程序性细胞死亡(PD-1)或程序性细胞死亡配体1(PD-L1)抑制剂,可作为一线、二线或维持治疗。UCC通常仍然无法治愈,并与内在和获得性药物及免疫耐药相关。UCC在转移状态下具有致命性,其特征为基因组不稳定、高PD-L1表达、DNA损伤反应突变以及高肿瘤突变负担。尽管免疫检查点抑制剂(ICIs)在其他癌症中能实现长期持久反应,但它们在转移性UCC(mUCC)中取得类似结果的能力尚不明确。在此,我们讨论改善UCC管理的治疗方法,以及全面的肿瘤分析如何识别可操作的生物标志物,并最终实现UCC患者精准医学的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3194/10571746/43c9d3f284df/cancers-15-04886-g001.jpg

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