Department of Genitourinary Medical Oncology, The University of Texas M. D. Anderson Cancer Center, 1155 Pressler Street, Houston, TX 77030, USA.
Curr Oncol Rep. 2010 Jul;12(4):278-83. doi: 10.1007/s11912-010-0104-5.
Since the advent of cisplatin-based chemotherapy, cytotoxic combination chemotherapy remains the mainstay of treatment for locally advanced and metastatic urothelial malignancies. The current paradigm of combining novel agents with cytotoxic chemotherapy without any understanding of the underlying biology of urothelial cancer has limited the impact of developing novel agents for this disease. Current research investigating the biology of bladder cancer, including the role of p53, EMT, EGFR-related pathways, and anti-angiogenic pathways, may potentially impact the future development of novel agents targeting urothelial malignancies. Additionally, the use of novel gene therapy to mediate enhanced interferon expression in the bladder using adenoviral vectors, and enhancing tumor recognition strategies using the immune system with vaccines and anti-CTLA4 antibodies, are of interest. It is hoped that through these efforts we may soon move beyond the traditional cytotoxic chemotherapy paradigm, developing combinations that are more active and less toxic for all patients with urothelial cancer.
自从顺铂为基础的化疗问世以来,细胞毒性联合化疗仍然是局部晚期和转移性尿路上皮恶性肿瘤的主要治疗方法。目前,将新型药物与细胞毒性化疗联合使用的模式,没有任何对尿路上皮癌生物学基础的了解,这限制了为这种疾病开发新型药物的影响。目前正在研究膀胱癌的生物学,包括 p53、EMT、EGFR 相关途径和抗血管生成途径,这可能会对靶向尿路上皮恶性肿瘤的新型药物的未来发展产生影响。此外,使用新型基因疗法,使用腺病毒载体介导膀胱中干扰素的表达增强,以及使用疫苗和抗 CTLA4 抗体增强免疫系统对肿瘤的识别策略,都很有意义。希望通过这些努力,我们能够很快超越传统的细胞毒性化疗模式,为所有尿路上皮癌患者开发更有效和毒性更小的联合治疗方案。