Denosumab combined with en bloc resection and arthrodesis for recurrent grade 3 giant cell tumor of bone in distal radius.
Humans
Female
Denosumab
/ therapeutic use
Male
Giant Cell Tumor of Bone
/ surgery
Radius
/ surgery
Adult
Retrospective Studies
Arthrodesis
/ methods
Bone Neoplasms
/ surgery
Neoplasm Recurrence, Local
Young Adult
Middle Aged
Treatment Outcome
Combined Modality Therapy
Follow-Up Studies
Bone Density Conservation Agents
/ therapeutic use
Neoplasm Grading
Bone Transplantation
/ methods
Arthrodesis
Denosumab
Distal radiusl Campanacci III
Recurrent GCTB
Journal
Journal of orthopaedic surgery and research
ISSN: 1749-799X
Titre abrégé: J Orthop Surg Res
Pays: England
ID NLM: 101265112
Informations de publication
Date de publication:
28 Sep 2024
28 Sep 2024
Historique:
received:
12
07
2024
accepted:
17
09
2024
medline:
29
9
2024
pubmed:
29
9
2024
entrez:
28
9
2024
Statut:
epublish
Résumé
This study aimed to analyse the clinical outcomes of preoperative adjuvant denosumab therapy (PADT) combined with resection and arthrodesis for recurrent grade 3 giant cell tumor of bone (GCTB) in the distal radius. A retrospective study was conducted on twenty-three patients (8 males, 15 females) who were treated with the adjuvant denosumab combined with en bloc resection (EBR) and arthrodesis for biopsy confirmed recurrent Campanacci III giant cell tumor of bone in the distal radius between January 2015 and December 2022. All 23 patients were treated with wrist arthrodesis reconstruction using autogenous free iliac crest bone graft (ICBG), bridging plate and screws. The local control, metastasis and overall survival were evaluated during the follow-up period. Functional outcomes were evaluated using the Disabilities of the Arm, Shoulder and Hand (DASH) score, Musculoskeletal Tumor Society Score (MSTS-87 and MSTS-93), and grip strength in the follow-up period. Additionally, all surgical or denosumab-related complications that occurred were recorded in this study. Twenty-three patients were included in this retrospective study and no patients were lost in the follow-up period. The average patient age was 32.5 ± 10.2 years (range, 19-53 years) and the mean follow-up time was 35.5 ± 18.4 months (range, 13-72 months). The average tumor length was 71.7 ± 8.7 mm (range, 50 to 85 mm) and bone reconstruction length was 78.5 ± 8.5 mm (range, 60 to 90 mm). Four patients (17.4%) had secondary local recurrence after reoperation and two patients had (8.7%) multiple recurrences. One patient (4.3%) was deceased in the last follow-up due to multiple metastases. The estimated 5-year recurrence-free survival rate was 81.3% and 5-year metastasis-free survival rate was 95.7%. The mean union time was 8.5 ± 1.9 (6-12) months and the overall survivorship of the allograft was 82.7% (21/23) at an average 35 month follow-up. The average MSTS-87 and MSTS-93 scores were 27.8 ± 1.6 (range, from 23 to 30) and 91.5 ± 5.0 (range, from 76 to 100), and the average DASH score was 8.9 ± 3.2 (range, from 3 to 15), respectively. The average grip strength was 64.6 ± 15.7% (range, from 30 to 95%) of the uninvolved side. Eight patients (34.7%) had at least one complication in the follow-up time. Two autografts (8.7%) were removed due to local recurrence and bone nonunion, and the average autograft survival time was 32.8 ± 18.5 months (range, 12 to 72 months). Preoperative adjuvant denosumab therapy (PADT) combined with en bloc resection and arthrodesis is a promising method for the treatment of recurrent Campanacci III GCTB in distal radius with acceptable short-term local control and functional satisfaction. level IV Therapeutic.
Identifiants
pubmed: 39342379
doi: 10.1186/s13018-024-05092-1
pii: 10.1186/s13018-024-05092-1
doi:
Substances chimiques
Denosumab
4EQZ6YO2HI
Bone Density Conservation Agents
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
607Subventions
Organisme : Key Technologies Research and Development Program
ID : 2023YFB4706300
Organisme : Key Technologies Research and Development Program
ID : 2023YFB4706300
Organisme : Key Technologies Research and Development Program
ID : 2023YFB4706300
Organisme : Key Technologies Research and Development Program
ID : 2023YFB4706300
Organisme : Key Technologies Research and Development Program
ID : 2023YFB4706300
Organisme : Key Technologies Research and Development Program
ID : 2023YFB4706300
Organisme : Key Technologies Research and Development Program
ID : 2023YFB4706300
Organisme : National Natural Science Foundation of China
ID : 62171017
Organisme : National Natural Science Foundation of China
ID : 62171017
Organisme : National Natural Science Foundation of China
ID : 62171017
Organisme : National Natural Science Foundation of China
ID : 62171017
Organisme : National Natural Science Foundation of China
ID : 62171017
Organisme : National Natural Science Foundation of China
ID : 62171017
Organisme : National Natural Science Foundation of China
ID : 62171017
Organisme : Beijing Municipal Natural Science Foundation
ID : L212042
Organisme : Beijing Municipal Natural Science Foundation
ID : L212042
Organisme : Beijing Municipal Natural Science Foundation
ID : L212042
Organisme : Beijing Municipal Natural Science Foundation
ID : L212042
Organisme : Beijing Municipal Natural Science Foundation
ID : L212042
Organisme : Beijing Municipal Natural Science Foundation
ID : L212042
Organisme : Beijing Municipal Natural Science Foundation
ID : L212042
Organisme : Beijing Municipal Health Commission
ID : BJRITO-RDP-2024
Informations de copyright
© 2024. The Author(s).
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