Targeting Signaling Transduction Pathways in Bladder Cancer

被引:30
作者
Abbosh, Phillip H. [1 ]
McConkey, David J. [2 ,3 ,4 ]
Plimack, Elizabeth R. [5 ]
机构
[1] Fox Chase Canc Ctr, Dept Surg Oncol, Div Urol Oncol, Philadelphia, PA 19111 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Urol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Canc Biol, Houston, TX 77030 USA
[4] Univ Texas Houston, Grad Sch Biomed Sci, Houston, TX 77030 USA
[5] Fox Chase Canc Ctr, Dept Med Oncol, Philadelphia, PA 19111 USA
关键词
Bladder cancer; Chemotherapy; Mutation; Copy number abnormality; EGFR; ERBB2; ERBB3; FGFR3; PIK3CA; mTOR; PTEN; Sunitinib; Pazopanib; Erlotinib; Cetuximab; Everolimus; Bevacizumab; Dovitinib; TRANSITIONAL-CELL CARCINOMA; GROWTH-FACTOR RECEPTOR-3; PHASE-II TRIAL; ABL TYROSINE KINASE; UROTHELIAL CARCINOMA; BREAST-CANCER; LUNG-CANCER; NEOADJUVANT CHEMOTHERAPY; ACTIVATING MUTATIONS; SELECTIVE INHIBITOR;
D O I
10.1007/s11912-015-0477-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Systemic therapy for urothelial carcinoma (UC) of the bladder has largely revolved around cytotoxic chemotherapy regimens. However, several recent clinical trials have explored the roles of targeted therapies which specifically inhibit signal transduction pathways. Simultaneously, a rationale for such therapies has come to the forefront of management of this disease because an overabundance of signaling pathways are genetically deranged as a result of point mutation or copy number alteration (CNA) as identified by several recent next generation sequencing (NGS) studies. Importantly, these derangements are found in all stages of disease, and therefore targeted therapies hold promise as a next step in the evolution of the medical management of both localized and metastatic UCC. We review the rationale for and progress in studying inhibition of signal transduction as a means of treatment of UCC.
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页数:10
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