C.H.J. Scholte , K. van Langevelde , D.M.J. Dorleijn , M. Fiocco , D. Broekhuis , P.D.S. Dijkstra , M.A.J. van de Sande , R.J.P. van der Wal
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引用次数: 0
Abstract
Purpose
Atypical cartilaginous tumors (ACT) are locally aggressive, cartilage-producing neoplasms, traditionally classified as chondrosarcoma grade 1. They exist within the spectrum of cartilaginous tumors, between enchondroma and high-grade chondrosarcoma. The diagnosis of ACT remains challenging, with limited consensus on optimal treatment. Despite ongoing debate, intralesional curettage is commonly performed, though the risk of pathological fractures post-treatment remains a significant complication. This study aims to investigate the impact of cortical window design on fracture risk following curettage for ACT in the distal femur.
Methods
We compared two types of cortical windows: smooth oval (low stress riser) and windows with sharp or predrilled rounded corners (high stress riser). A retrospective cohort of 153 patients treated between 2000 and 2020 was included. Fracture occurrence was recorded, and logistic regression models were used to assess the relationship between surgical technique and fracture risk. We corrected for void filling and tumour size.
Results
Our findings revealed no significant difference in fracture risk between the two types of cortical windows (OR = 1.62, 95 % CI:0.66–3.96). However, the use of cement as a void filler significantly increased fracture risk, with odds ratio (OR) approximately five times higher than those using bone chips (OR = 5.00, 95 % CI:1.81–13.88). Tumor size (cm) was also associated with fracture risk (OR 1.31, 95 % CI:1.04–1.63).
Conclusion
The study highlights the importance of choosing appropriate void filling material, with bone chips offering a lower fracture risk compared to cement. These results suggest that optimizing surgical techniques, particularly the choice of filling material, may reduce post-curettage fracture risk in ACT treatment.
期刊介绍:
The Journal of Bone Oncology is a peer-reviewed international journal aimed at presenting basic, translational and clinical high-quality research related to bone and cancer.
As the first journal dedicated to cancer induced bone diseases, JBO welcomes original research articles, review articles, editorials and opinion pieces. Case reports will only be considered in exceptional circumstances and only when accompanied by a comprehensive review of the subject.
The areas covered by the journal include:
Bone metastases (pathophysiology, epidemiology, diagnostics, clinical features, prevention, treatment)
Preclinical models of metastasis
Bone microenvironment in cancer (stem cell, bone cell and cancer interactions)
Bone targeted therapy (pharmacology, therapeutic targets, drug development, clinical trials, side-effects, outcome research, health economics)
Cancer treatment induced bone loss (epidemiology, pathophysiology, prevention and management)
Bone imaging (clinical and animal, skeletal interventional radiology)
Bone biomarkers (clinical and translational applications)
Radiotherapy and radio-isotopes
Skeletal complications
Bone pain (mechanisms and management)
Orthopaedic cancer surgery
Primary bone tumours
Clinical guidelines
Multidisciplinary care
Keywords: bisphosphonate, bone, breast cancer, cancer, CTIBL, denosumab, metastasis, myeloma, osteoblast, osteoclast, osteooncology, osteo-oncology, prostate cancer, skeleton, tumour.