Renal-cell carcinoma: tumour markers, T-cell epitopes, and potential for new therapies

被引:45
作者
Michael, A [1 ]
Pandha, HS [1 ]
机构
[1] St George Hosp, Sch Med, Dept Oncol, London SW17 0RE, England
关键词
D O I
10.1016/S1470-2045(03)01044-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Advanced renal-cell carcinoma is a very difficult tumour to treat, and response rates to biological therapies are less than 20%. The identification of various molecular and cellular markers has led to the development of novel therapies. Despite evaluation of their association with histological subtype, immune infiltration, molecular markers of cell proliferation, p53 mutation, and growth-factor-receptor expression, none of these markers has proved better predictive factors than tumour stage and histological grade. The identification of tumour-associated antigens and the specificity of cellular immune responses have led to the development of targeted immunotherapy with monoclonal antibodies, radioimmunotherapy, and T-cell therapies. In this review, we evaluate a range of markers associated with renal-cell carcinoma and new treatment approaches based on tumour-associated antigens and, in particular, T-cell epitopes.
引用
收藏
页码:215 / 223
页数:9
相关论文
共 107 条
[21]  
Fujita H, 1998, EUR J IMMUNOL, V28, P305, DOI 10.1002/(SICI)1521-4141(199801)28:01<305::AID-IMMU305>3.0.CO
[22]  
2-3
[23]  
Gaugler B, 1996, IMMUNOGENETICS, V44, P323, DOI 10.1007/BF02602776
[24]  
Gelb AB, 1997, CANCER-AM CANCER SOC, V80, P1768, DOI 10.1002/(SICI)1097-0142(19971101)80:9<1768::AID-CNCR11>3.0.CO
[25]  
2-3
[26]  
Gilcrease MZ, 1999, CANCER-AM CANCER SOC, V86, P2320, DOI 10.1002/(SICI)1097-0142(19991201)86:11<2320::AID-CNCR20>3.0.CO
[27]  
2-0
[28]  
Gjertsen MK, 1997, INT J CANCER, V72, P784, DOI 10.1002/(SICI)1097-0215(19970904)72:5<784::AID-IJC14>3.3.CO
[29]  
2-G
[30]   Induction of antitumor activity by immunization with fusions of dendritic and carcinoma cells [J].
Gong, JL ;
Chen, DS ;
Kashiwaba, M ;
Kufe, D .
NATURE MEDICINE, 1997, 3 (05) :558-561