Bisphosphonate treatment of aggressive primary, recurrent and metastatic Giant Cell Tumour of Bone
Creators
- 1. Department of Orthopaedic Surgery, University of Munster, Albert-Schweitzer-Str. 3, 48149 Munster (Germany)
- 2. University of Oxford, Nuffield Department of Orthopaedic Surgery, Department of Pathology, Nuffield Orthopaedic Centre, Oxford, OX3 7LD (United Kingdom)
- 3. Laboratory of Oncologic Research, Orthopaedic Institute Rizzoli, Via di Barbiano 1/10, 40136 Bologna (Italy)
- 4. Department of Pathology, Leiden University Medical Centre, Albinusdreef 2, Leiden, P.O. Box 9600, L1-Q, 2300 RC Leiden (Netherlands)
Description
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
Availability note (English)
Available from http://dx.doi.org/10.1186/1471-2407-10-462; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940802Additional details
Identifiers
Publishing Information
- Journal Title
- BMC cancer (Online)
- Journal Volume
- 10
- Journal Page Range
- p. 462
- ISSN
- 1471-2407
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46098625
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- DRUGS; IN VITRO; LUNGS; METASTASES; REFRACTORIES; SKELETON; TUMOR CELLS
- Descriptors DEC
- ANIMAL CELLS; BODY; ORGANS; RESPIRATORY SYSTEM
Optional Information
- Copyright
- Copyright (c)2010 Balke et al
- Notes
- PMCID: PMC2940802; PUBLISHER-ID: 1471-2407-10-462; PMID: 20799989; OAI: oai:pubmedcentral.nih.gov:2940802; licensee BioMed Central Ltd.