Miller Eric J, Galsky Matthew D
Division of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai/Tisch Cancer Institute, New York, NY, 10029, USA.
Curr Treat Options Oncol. 2023 Dec;24(12):1870-1888. doi: 10.1007/s11864-023-01151-7. Epub 2023 Dec 12.
The treatment landscape for urothelial cancer has changed dramatically in the last 10 years, with the approval of several new treatments. At the same time, profiling of individual tumors has become more commonplace with widespread availability of molecular testing and immunohistochemistry. For urothelial cancer, this has led to current guidelines recommending that molecular testing be obtained in the metastatic setting, and that it be considered in the setting of locally advanced disease. Between molecular testing and immunohistochemistry testing of tumors, the only current guideline-directed application of these tests is in the identification of FGFR3 or FGFR2 alterations for use of FGFR inhibitors. While additional recurrent molecular alterations linked to the pathogenesis of urothelial cancer have been identified, the ability to successfully "drug" the pathways association with such alterations remains limited. There has been extensive research into whether expression of particular proteins might inform specific treatment approaches such as the use of PD-L1 testing to guide immune checkpoint blockade. With the integration of antibody-drug conjugates into the treatment armamentarium for urothelial cancer, ongoing research is seeking to determine whether expression of the targets of these therapies, such as Nectin 4, Trop-2, or HER2, could help to guide treatment.
在过去10年中,随着几种新疗法的获批,尿路上皮癌的治疗格局发生了巨大变化。与此同时,随着分子检测和免疫组织化学的广泛应用,对个体肿瘤进行分析已变得更为普遍。对于尿路上皮癌而言,这导致当前指南建议在转移性疾病情况下进行分子检测,并在局部晚期疾病情况下予以考虑。在肿瘤的分子检测和免疫组织化学检测之间,目前这些检测唯一遵循指南的应用是识别FGFR3或FGFR2改变,以使用FGFR抑制剂。虽然已经确定了与尿路上皮癌发病机制相关的其他复发性分子改变,但成功“靶向治疗”与此类改变相关途径的能力仍然有限。对于特定蛋白质的表达是否可能为特定治疗方法提供依据,例如使用PD-L1检测来指导免疫检查点阻断,已经进行了广泛研究。随着抗体药物偶联物被纳入尿路上皮癌的治疗手段,正在进行的研究试图确定这些疗法的靶点,如Nectin 4、Trop-2或HER2的表达是否有助于指导治疗。