Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Jul;3(7):515-528.
doi: 10.1302/2633-1462.37.BJO-2022-0064.R1.

Surgical challenges, novel techniques, and systemic treatment of giant cell tumour of bone of the distal radius : clinical outcomes and systematic review of the literature

Affiliations

Surgical challenges, novel techniques, and systemic treatment of giant cell tumour of bone of the distal radius : clinical outcomes and systematic review of the literature

Lizz van der Heijden et al. Bone Jt Open. 2022 Jul.

Abstract

Aims: Giant cell tumour of bone (GCTB) treatment changed since the introduction of denosumab from purely surgical towards a multidisciplinary approach, with recent concerns of higher recurrence rates after denosumab. We evaluated oncological, surgical, and functional outcomes for distal radius GCTB, with a critically appraised systematic literature review.

Methods: We included 76 patients with distal radius GCTB in three sarcoma centres (1990 to 2019). Median follow-up was 8.8 years (2 to 23). Seven patients underwent curettage, 38 curettage with adjuvants, and 31 resection; 20 had denosumab.

Results: Recurrence rate was 71% (5/7) after curettage, 32% (12/38) after curettage with adjuvants, and 6% (2/31) after resection. Median time to recurrence was 17 months (4 to 77). Recurrences were treated with curettage with adjuvants (11), resection (six), or curettage (two). Overall, 84% (38/45) was cured after one to thee intralesional procedures. Seven patients had 12 months neoadjuvant denosumab (5 to 15) and sixmonths adjuvant denosumab; two recurred (29%). Twelve patients had six months neoadjuvant denosumab (4 to 10); five recurred (42%). Two had pulmonary metastases (2.6%), both stable after denosumab. Complication rate was 18% (14/76, with 11 requiring surgery). At follow-up, median MusculoSkeletal Tumour Society score was 28 (18 to 30), median Short Form-36 Health Survey was 86 (41 to 95), and median Disability of Arm, Shoulder, and Hand was 7.8 (0 to 58).

Conclusion: Distal radius GCTB treatment might deviate from general GCTB treatment because of complexity of wrist anatomy and function. Novel insights on surgical treatment are presented in this multicentre study and systematic review. Intralesional surgery resulted in high recurrence-rate for distal radius GCTB, also with additional denosumab. The large majority of patients however, were cured after repeated curettage. Cite this article: Bone Jt Open 2022;3(7):515-528.

Keywords: Denosumab; MusculoSkeletal Tumour Society score; Short Form 36; curettage; denosumab; distal radius; functional outcomes; giant cell tumor of bone; giant cell tumour of bone; neoadjuvant denosumab; resection; surgical approaches; wrist.

PubMed Disclaimer

Conflict of interest statement

ICMJE COI statement: All authors declare that they have no conflicts of interest related to this work.

Figures

Fig. 1
Fig. 1
35-year-old patient with conventional giant cell tumour of the distal radius, without cortical breakthrough nor soft-tissue extension. Treatment consisted of extended curettage with high-speed burring, phenol and filling of the remaining cavity with bone cement. There were no recurrences nor complications during follow-up.
Fig. 2
Fig. 2
a) 32-year-old patient with high-risk giant cell tumour of of the distal radius with cortical thinning, soft-tissue extension, and disturbed radiocarpal alignment. b) En bloc resection was performed with arthrodesis with a tibia strut autograft and screw fixation. c) Radiographs at five-year follow-up show complete fusion of both radiocarpal arthrodesis and proximal bone junction, with remodelling of the graft.
Fig. 3
Fig. 3
a) 36-year-old patient with high-risk giant cell tumour of of the distal radius with cortical thinning and soft-tissue extension. b) En bloc resection was performed with wrist arthrodesis with osteoarticular allograft and plate fixation. There were no recurrences nor complications during 15-year follow-up.
Fig. 4
Fig. 4
a) 36-year-old patient with high-risk giant cell tumour of the distal radius with cortical thinning and very large soft-tissue component. b) En bloc resection was performed with wrist arthrodesis with a free vascularized fibula autograft and plate fixation. This patient developed pulmonary metastases, treated with continuous denosumab. Otherwise, there were no recurrences nor complications during ten-year follow-up.
Fig. 5
Fig. 5
Flowchart of systematic literature review following Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines.
Fig. 6
Fig. 6
Flowchart of treatment for primary distal radius giant cell tumour of bone and their recurrences.

References

    1. Athanasou NA, Bansal M, Forsyth R, et al. . Giant cell tumour of bone. In Fletcher CDM, Bridge JA, Hogendoorn PCW, Mertens F. WHO Classification of Tumours of Soft Tissue and Bone. IARC WHO Classification of Tumours Series. 5. 4 ed. Lyon: International Agency for Research on Cancer (IARC), 2013: 321–324.
    1. Verschoor AJ, Bovée J, Mastboom MJL, Sander Dijkstra PD, Van De Sande MAJ, Gelderblom H, et al. . Incidence and demographics of giant cell tumor of bone in the Netherlands: First nationwide pathology registry study. Acta Orthop. 2018;89(5):570–574. 10.1080/17453674.2018.1490987 - DOI - PMC - PubMed
    1. Alberghini M, Kliskey K, Krenacs T, et al. . Morphological and immunophenotypic features of primary and metastatic giant cell tumour of bone. Virchows Arch. 2010;456(1):97–103. 10.1007/s00428-009-0863-2 - DOI - PubMed
    1. Tubbs WS, Brown LR, Beabout JW, Rock MG, Unni KK, et al. . Benign giant-cell tumor of bone with pulmonary metastases: clinical findings and radiologic appearance of metastases in 13 cases. AJR Am J Roentgenol. 1992;158(2):331–334. 10.2214/ajr.158.2.1729794 - DOI - PubMed
    1. Siebenrock KA, Unni KK, Rock MG. Giant-cell tumour of bone metastasising to the lungs. A long-term follow-up. J Bone Joint Surg Br. 1998;80-B(1):43–47. 10.1302/0301-620x.80b1.7875 - DOI - PubMed