Published August 29, 2010 | Version v1
Journal article

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

  • 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/PMC2940802

Additional details

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.