Broad clinical activity of zoledronic acid in osteolytic to osteoblastic bone lesions in patients with a broad range of solid tumors

被引:15
作者
Rosen, L
Harland, SJ
Oosterlinck, W
机构
[1] John Wayne Canc Inst, Santa Monica, CA 90404 USA
[2] UCL, Dept Oncol, London, England
[3] Ghent Univ Hosp, Dept Urol, B-9000 Ghent, Belgium
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 2002年 / 25卷 / 06期
关键词
bone metastasis; breast cancer; prostate cancer; solid tumor; zoledronic acid;
D O I
10.1097/00000421-200212001-00004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Bone metastases are a common feature of a variety of solid tumors and are associated with substantial skeletal morbidity, including severe bone pain and pathologic fractures. Treatment with bisphosphonates, primarily pamidronate, is the current standard of care for patients with breast cancer and multiple myeloma who have predominantly osteolytic lesions. However, until recently no bisphosphonate had demonstrated efficacy in patients with osteoblastic lesions, which are common during the progression of prostate cancer and other solid tumors. Zoledronic acid, a potent, new-generation, nitrogen-containing bisphosphonate, has demonstrated significant benefits for patients with bone metastases resulting from a broad range of primary tumors, including multiple myeloma and breast, lung, kidney, and prostate cancers, and other solid tumors. Benefits include a decreased incidence of pathologic fractures and longer time to the first skeletal complication. Zoledronic acid is the first and only bisphosphonate to be proved effective in patients with all types of bone lesions, from osteolytic to osteoblastic. and therefore represents an important therapeutic advancement in the treatment of bone metastases.
引用
收藏
页码:S19 / S24
页数:6
相关论文
共 38 条
[1]  
Berruti A, 1999, CLIN CHEM, V45, P1240
[2]   Incidence of skeletal complications in patients with bone metastatic prostate cancer and hormone refractory disease: Predictive role of bone resorption and formation markers evaluated at baseline [J].
Berruti, A ;
Dogliotti, L ;
Bitossi, R ;
Fasolis, G ;
Gorzegno, G ;
Bellina, M ;
Torta, M ;
Porpiglia, F ;
Fontana, D ;
Angeli, A .
JOURNAL OF UROLOGY, 2000, 164 (04) :1248-1253
[3]   THE CLINICAL COURSE OF BONE METASTASES FROM BREAST-CANCER [J].
COLEMAN, RE ;
RUBENS, RD .
BRITISH JOURNAL OF CANCER, 1987, 55 (01) :61-66
[4]   The clinical use of bone resorption markers in patients with malignant bone disease [J].
Coleman, RE .
CANCER, 2002, 94 (10) :2521-2533
[5]   Should bisphosphonates be the treatment of choice for metastatic bone disease? [J].
Coleman, RE .
SEMINARS IN ONCOLOGY, 2001, 28 (04) :35-41
[6]  
Coleman RE, 1997, CANCER, V80, P1588, DOI 10.1002/(SICI)1097-0142(19971015)80:8+<1588::AID-CNCR9>3.3.CO
[7]  
2-Z
[8]  
COLEMAN RE, 2002, 25 ANN SAN ANT BREAS
[9]  
DEMERS LM, 1995, CLIN CHEM, V41, P1489
[10]  
ERNST DS, 2002, P AN M AM SOC CLIN, V21, pA177