Current therapeutic strategies for invasive and metastatic bladder cancer

被引:37
|
作者
Vishnu, Prakash [1 ]
Mathew, Jacob [1 ]
Tan, Winston W. [1 ]
机构
[1] Mayo Clin, Div Hematol Oncol, Jacksonville, FL 32224 USA
来源
ONCOTARGETS AND THERAPY | 2011年 / 4卷
关键词
bladder cancer; chemotherapy; biologic therapy; neoadjuvant; PI3kinase/mTOR pathway; TRANSITIONAL-CELL-CARCINOMA; PHASE-III TRIAL; GEMCITABINE PLUS CISPLATIN; ADVANCED UROTHELIAL CANCER; COLONY-STIMULATING FACTOR; TERM-FOLLOW-UP; RADICAL CYSTECTOMY; NEOADJUVANT CHEMOTHERAPY; URINARY-BLADDER; RANDOMIZED-TRIAL;
D O I
10.2147/OTT.S22875
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Bladder cancer is one of the most common cancers in Europe, the United States, and Northern African countries. Muscle-invasive bladder cancer is an aggressive epithelial tumor, with a high rate of early systemic dissemination. Superficial, noninvasive bladder cancer can most often be cured; a good proportion of invasive cases can also be cured by a combined modality approach of surgery, chemotherapy, and radiation. Recurrences are common and mostly manifest as metastatic disease. Those with distant metastatic disease can sometime achieve partial or complete remission with combination chemotherapy. Recent developments: Better understanding of the biology of the disease has led to the incorporation of molecular and genetic features along with factors such as tumor grade, lymphovascular invasion, and aberrant histology, thereby allowing identification of 'favorable' and 'unfavorable' cancers which helps a more accurate informed and objective selection of patients who would benefit from neoadjuvant and adjuvant chemotherapy. Gene expression profiling has been used to find molecular signature patterns that can potentially be predictive of drug sensitivity and metastasis. Understanding the molecular pathways of invasive bladder cancer has led to clinical investigation of several targeted therapeutics such as anti-angiogenics, mTOR inhibitors, and anti-EGFR agents. Conclusion: With improvements in the understanding of the biology of bladder cancer, clinical trials studying novel and targeted agents alone or in combination with chemotherapy have increased the armamentarium for the treatment of bladder cancer. Although the novel biomarkers and gene expression profiles have been shown to provide important predictive and prognostic information and are anticipated to be incorporated in clinical decision-making, their exact utility and relevance calls for a larger prospective validation.
引用
收藏
页码:97 / 113
页数:17
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