Chemotherapy and novel therapeutic approaches in malignant gliomas

被引:45
作者
Desjardins, A
Rich, JN
Quinn, JA
Vredenburgh, J
Gururangan, S
Sathornsumetee, S
Reardon, DA
Friedman, AH
Bigner, DD
Friedman, HS
机构
[1] Duke Univ, Med Ctr, Brain Tumor Ctr Duke, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Pediat, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Neurol, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[5] Duke Univ, Med Ctr, Dept Neurosurg, Durham, NC 27710 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2005年 / 10卷
关键词
tumor; cancer; glial cells; malignant; gliomas; radiation therapy; chemotherapy; tyrosine kinase inhibitors; review;
D O I
10.2741/1727
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glial neoplasms represent 0.5-1% of all cancers in most Western countries. Malignant gliomas are among the most devastating cancers, leading to death in most cases. They present unique challenges due to their location, aggressive biological behavior and diffuse infiltrative growth. Notwithstanding the development of new surgical and radiation techniques in the last thirty years, a cure for malignant gliomas remains elusive. In this article, we will review the standard and new therapies used for malignant gliomas. As standard therapies, surgery, radiation therapy and systemic chemotherapy, are in a continuous process of evolution. Multiple chemotherapies have been used in malignant gliomas, as single agents, in combination, or with different modes of administration, including high-dose chemotherapy with stem cell rescue and intraarterial chemotherapy. The last decade has been noticeable for the advent of a better understanding of the biology of malignant gliomas. This has stimulated active research in multiples areas and the advent of new treatment strategies. Techniques to circumvent the resistance mechanisms to chemotherapy have been evaluated, tyrosine kinase inhibitors have shown activity in malignant primary brain tumors and radioimmunotherapy remains an area of active research. In this article, we review the past, present and future treatments of malignant gliomas with a special interest on chemotherapy, resistance mechanisms and tyrosine kinase inhibitors.
引用
收藏
页码:2645 / 2668
页数:24
相关论文
共 129 条
[111]  
Soulie P, 1997, B CANCER, V84, P665
[112]  
STUPP R, 2004, 40 ANN M AM SOC CLIN
[113]  
UHM JH, 2004, 49 ANN M AM SOC CLIN
[114]  
Uhrbom L, 1998, CANCER RES, V58, P5275
[115]  
VOGELBAUM M, 2003, 8 ANN M SOC NEUR KEY
[116]   RANDOMIZED COMPARISONS OF RADIOTHERAPY AND NITROSOUREAS FOR THE TREATMENT OF MALIGNANT GLIOMA AFTER SURGERY [J].
WALKER, MD ;
GREEN, SB ;
BYAR, DP ;
ALEXANDER, E ;
BATZDORF, U ;
BROOKS, WH ;
HUNT, WE ;
MACCARTY, CS ;
MAHALEY, MS ;
MEALEY, J ;
OWENS, G ;
RANSOHOFF, J ;
ROBERTSON, JT ;
SHAPIRO, WR ;
SMITH, KR ;
WILSON, CB ;
STRIKE, TA .
NEW ENGLAND JOURNAL OF MEDICINE, 1980, 303 (23) :1323-1329
[117]   O-6-Benzylguanine enhances the sensitivity of a glioma xenograft with low O-6-alkylguanine-DNA alkyltransferase activity to temozolomide and BCNU [J].
Wedge, SR ;
Newlands, ES .
BRITISH JOURNAL OF CANCER, 1996, 73 (09) :1049-1052
[118]   3-aminobenzamide and/or O-6-benzylguanine evaluated as an adjuvant to temozolomide or BCNU treatment in cell lines of variable mismatch repair status and O-6-alkylguanine-DNA alkyltransferase activity [J].
Wedge, SR ;
Porteous, JK ;
Newlands, ES .
BRITISH JOURNAL OF CANCER, 1996, 74 (07) :1030-1036
[119]  
WEN PY, 2002, 38 ANN M AM SOC CLIN
[120]   O-6-ALKYLGUANINE-DNA ALKYLTRANSFERASE ACTIVITY IN HUMAN-BRAIN AND BRAIN-TUMORS [J].
WIESTLER, O ;
KLEIHUES, P ;
PEGG, AE .
CARCINOGENESIS, 1984, 5 (01) :121-124