header advert
Results 1 - 2 of 2
Results per page:
Orthopaedic Proceedings
Vol. 103-B, Issue SUPP_3 | Pages 76 - 76
1 Mar 2021
Malik A Alexander J Khan S Scharschmidt T
Full Access

The management of primary malignant bone tumors with metastatic disease at presentation remains a challenge. While surgical resection has been shown to improve overall survival among patients with non-metastatic malignant bone tumors, current evidence regarding the utility of surgery in improving overall survival in metastatic patients remains limited.

The 2004–2016 National Cancer Database (NCDB) was queried using International Classification of Diseases 3rd Edition (ICD-O-3) topographical codes to identify patients with primary malignant bone tumors of the extremities (C40.0-C40.3, C40.8 and C40.9) and/or pelvis (C41.4). Patients with malignant bone tumors of the axial skeleton (head/skull, trunk and spinal column) were excluded, as these cases are not routinely encountered and/or managed by orthopaedic oncologists. Histological codes were used to categorize the tumors into the following groups - osteosarcomas, chondrosarcomas, and Ewing sarcomas. Patients who were classified as stage I, II or III, based on American Joint Commission of Cancer (AJCC) guidelines, were excluded. Only patients with metastatic disease at presentation were included in the final study sample. The study sample was divided into two distinct groups – those who underwent surgical resection of the primary tumors vs. those who did not receive any surgery of the primary tumor. Kaplan-Meier survival analysis was used to report unadjusted 5-year overall survival rates between patients who underwent surgical resection of the primary tumor, compared to those who did not. Multi-variate Cox regression analyses were used to assess whether undergoing surgical resection of the primary tumor was associated with improved overall survival, after controlling for differences in baseline demographics, tumor characteristics (grade, location, histological type and tumor size), and treatment patterns (underwent metastatectomy of distal and/or regional sites, positive vs. negative surgical margins, use of radiation therapy and/or chemotherapy). Additional sensitivity analyses, stratified by histologic type for osteosarcomas, chondrosarcomas and Ewing sarcomas, were used to assess prognostic factors for overall survival.

A total of 2,288 primary malignant bone tumors (1,121 osteosarcomas, 345 chondrosarcomas, and 822 Ewing sarcomas) with metastatic disease at presentation were included – out of which 1,066 (46.0%) underwent a surgical resection of the primary site. Overall 5-year survival rates, on unadjusted Kaplan-Meier log-rank analysis, were significantly better for individuals who underwent surgical resection vs. those who did not receive any surgery (31.7% vs. 17.3%; p<0.001). After controlling for differences in baseline demographics, tumor characteristics and treatment patterns, undergoing surgical resection of primary site was associated with a reduced overall mortality (HR 0.42 [95% CI 0.36–0.49]; p<0.001). Undergoing metastectomy (HR 0.92 [95% CI 0.81–1.05]; p=0.235) was not associated with a significant improvement in overall survival. On stratified analysis, radiation therapy was associated with improved overall survival for Ewing Sarcoma (HR 0.71 [95% CI 0.57–0.88]; p=0.002), but not for osteosarcoma (HR 1.14 [95% CI 0.91–1.43]; p=0.643) or chondrosarcoma (HR 1.08 [95 % CI 0.78–1.50]; p=0.643). Chemotherapy was associated with improved overall survival for osteosarcoma (HR 0.50 [95% CI 0.39–0.64]; p<0.001) and chondrosarcoma (HR 0.62 [95% CI 0.45–0.85]; p=0.003), but not Ewing sarcoma (HR 0.79 [95% CI 0.46–1.35]; p=0.385).

Surgical resection of the primary site significantly improves overall survival for primary malignant bone tumors with metastatic disease at presentation. Physicians should strongly consider surgical resection of the primary tumor, with adjunct systemic and/or radiation therapy (dependent on tumor histology), in patients presenting with metastatic disease at presentation.


Orthopaedic Proceedings
Vol. 92-B, Issue SUPP_I | Pages 10 - 11
1 Mar 2010
Scharschmidt T Weiner D Jacquet R Lowder E Schrickel T Landis W
Full Access

Purpose: Slipped capital femoral epiphysis (SCFE) is a poorly understood condition impacting adolescents. Its consequences can be severe, even where there is early recognition and treatment is implemented. Prior studies have suggested that the etiology may be related to abnormal collagen comprising the growth plate cartilage, but no investigations have analyzed collagen or other structural proteins on a molecular level in the affected tissue. This study evaluates expression of mRNA for key structural proteins obtained from growth plate chondrocytes of patients suffering SCFE.

Method: The work utilizes laser capture microdissection (LCM) techniques followed by reverse transcription polymerase chain reaction (RT-PCR) to determine if a change or abnormality in type II collagen and/or aggrecan gene expression may be involved in weakening the physis, a characteristic of the pathology. With these techniques, correlation of chondrocyte spatial location and gene expression can be made to provide greater insight into this pathology and a more complete understanding of growth plate biology in general.

Results: Downregulation of both type II collagen and aggrecan was found in the growth plates of SCFE subjects when compared to age-matched controls. Expression levels for type II collagen mRNA of SCFE patients were less than 14% of their counterpart controls. SCFE aggrecan levels averaged only 26% of control expression.

Conclusion: The significant decreases in type II collagen and aggrecan expression would drastically affect the quantity, distribution, and organization of both components in SCFE growth plates. Such abnormal changes may contribute to the cause of a slip although possibly they may be the result of a slip. This is the first study using novel LCM and RT-PCR to determine specific gene expression levels for two principal structural proteins comprising the growth plates of human subjects suffering SCFE.