Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone.
Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone.
复制标题
DOI:
10.1186/1471-2407-10-462
复制
发表时间:
2010-08-29
期刊:
影响因子:
3.8
通讯作者:
Athanasou N
中科院分区:
文献类型:
--
作者:
Balke M;Campanacci L;Gebert C;Picci P;Gibbons M;Taylor R;Hogendoorn P;Kroep J;Wass J;Athanasou N
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. 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. 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. 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.
登录
查看更多内容
DOI:
10.2106/00004623-198769010-00018
发表时间:
1987-01-01
影响因子:
5.3
作者:
CAMPANACCI, M;BALDINI, N;SUDANESE, A
通讯作者:
SUDANESE, A
影响因子:
4.2
作者:
Cheng, YY;Huang, L;Kumta, SM
通讯作者:
Kumta, SM
影响因子:
51.1
作者:
Thomas, David;Henshaw, Robert;Jun, Susie
通讯作者:
Jun, Susie
影响因子:
6.2
作者:
Chapurlat, RD;Delmas, PD;Meunier, PJ
通讯作者:
Meunier, PJ
影响因子:
4.1
作者:
Nishikawa, M;Akatsu, T;Nagata, N
通讯作者:
Nagata, N