Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone

被引:107
作者
Balke, Maurice [2 ]
Campanacci, Laura [3 ]
Gebert, Carsten [2 ]
Picci, Piero [3 ]
Gibbons, Max [1 ]
Taylor, Richard [1 ]
Hogendoorn, Pancras [4 ]
Kroep, Judith [4 ]
Wass, John [1 ]
Athanasou, Nicholas [1 ]
机构
[1] Univ Oxford, Nuffield Dept Orthopaed Surg, Dept Pathol, Nuffield Orthopaed Ctr, Oxford OX3 7LD, England
[2] Univ Munster, Dept Orthopaed Surg, D-48149 Munster, Germany
[3] Orthopaed Inst Rizzoli, Lab Oncol Res, I-40136 Bologna, Italy
[4] Leiden Univ, Med Ctr, Dept Pathol, NL-2300 RC Leiden, Netherlands
来源
BMC CANCER | 2010年 / 10卷
关键词
FIBROUS DYSPLASIA; MECHANISMS; APOPTOSIS; PAMIDRONATE; OSTEOCLASTS; RESORPTION; THERAPY;
D O I
10.1186/1471-2407-10-462
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Giant cell tumour of bone (GCTB) is an expansile osteolytic tumour which contains numerous osteoclast-like giant cells. GCTB frequently recurs and can produce metastatic lesions in the lungs. Bisphosphonates are anti-resorptive drugs which act mainly on osteoclasts. Method: In this study, we have examined clinical and radiological outcomes of treatment with aminobisphosphonates on 25 cases of aggressive primary, recurrent and metastatic GCTB derived from four European centres. We also analysed in vitro the inhibitory effect of zoledronic acid on osteoclasts isolated from GCTBs. Results: Treatment protocols differed with several different aminobisphosphonates being employed, but stabilisation of disease was achieved in most of these cases which were refractory to conventional treatment. Most inoperable sacral/pelvic tumours did not increase in size and no further recurrence was seen in GCTBs that had repeatedly recurred in bone and soft tissues. Lung metastases did not increase in size or number following treatment. Zoledronic acid markedly inhibited lacunar resorption by GCTB-derived osteoclasts in vitro. Conclusion: Our findings suggest that bisphosphonates may be useful in controlling disease progression in GCTB and that these agents directly inhibit GCTB - derived osteoclast resorption. These studies highlight the need for the establishment of standardised protocols to assess the efficacy of bisphosphonate treatment of GCTB.
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页数:8
相关论文
共 30 条
[11]   Treatment of Langerhans cell histiocytosis with pamidronate [J].
Farran, RP ;
Zaretski, E ;
Egeler, RM .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2001, 23 (01) :54-56
[12]   Analgesia for patients with advanced disease: 2 [J].
Hall, EJ ;
Sykes, NP .
POSTGRADUATE MEDICAL JOURNAL, 2004, 80 (942) :190-195
[13]  
HUGHES DE, 1995, J BONE MINER RES, V10, P1478
[14]   Mechanism of action, pharmacokinetic and pharmacodynamic profile, and clinical applications of nitrogen-containing bisphosphonates [J].
Kimmel, D. B. .
JOURNAL OF DENTAL RESEARCH, 2007, 86 (11) :1022-1033
[15]  
Lane JM, 2001, CLIN ORTHOP RELAT R, P6
[16]   Phenotypic and molecular studies of giant-cell tumors of bone and soft tissue [J].
Lau, YS ;
Sabokbar, A ;
Gibbons, CLMH ;
Giele, H ;
Athanasou, N .
HUMAN PATHOLOGY, 2005, 36 (09) :945-954
[17]   Giant cell tumor of bone [J].
Mendenhall, WM ;
Zlotecki, RA ;
Scarborough, MT ;
Gibbs, CP ;
Mendenhall, NP .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2006, 29 (01) :96-99
[18]   Bisphosphonates act on osteoblastic cells and inhibit osteoclast formation in mouse marrow cultures [J].
Nishikawa, M ;
Akatsu, T ;
Katayama, Y ;
Yasutomo, Y ;
Kado, S ;
Kugai, N ;
Yamamoto, M ;
Nagata, N .
BONE, 1996, 18 (01) :9-14
[19]   Bisphosphonate inhibition of bone resorption induced by particulate biomaterial-associated macrophages [J].
Pandey, R ;
Quinn, JMW ;
Sabokbar, A ;
Athanasou, NA .
ACTA ORTHOPAEDICA SCANDINAVICA, 1996, 67 (03) :221-228
[20]  
PETRA M, 2003, SARCOMA, V7, P35