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dc.contributor.authorCoskun, Huseyin Sina
dc.contributor.authorErdogan, Furkan
dc.contributor.authorBuyukceran, Ismail
dc.contributor.authorDabak, Nevzat
dc.date.accessioned2024-03-12T19:34:53Z
dc.date.available2024-03-12T19:34:53Z
dc.date.issued2022
dc.identifier.issn2687-4784
dc.identifier.issn2687-4792
dc.identifier.urihttps://doi.org/10.52312/jdrs.2022.526
dc.identifier.urihttps://hdl.handle.net/20.500.12450/2757
dc.description.abstractObjectives: The aim of this study was to identify the demographic characteristics of chondrosarcoma (CS) and prognostic factors affecting survival. Patients and methods: A total of 87 patients (45 males, 42 females; median age: 51.3 years; range, 19 to 77 years) with CS treated in our clinic between January 2007 and June 2020 were retrospectively analyzed. Demographic characteristics, whether it was primary/secondary, tumor location, histopathological features, tumor grade and stage, clinical follow-up period, surgical treatment methods, use of radiotherapy and chemotherapy, and the presence of local recurrence and metastasis in the postoperative period were recorded. The relationship of these factors with prognosis was analyzed and survival rates were compared. Results: Histological subtype, tumor grade, pathological stage and presence of metastasis were defined as independent predictors in both overall survival and disease-free survival analysis of CS. Overall and disease-free five-year and 10-year survival rates were found to be the highest in the clear cell chondrosarcoma group. While mortality increased in the first five years in the patient groups with histological Grade 2 and 3, all groups were followed in a balanced manner over time. The mortality rate in the group with metastatic disease (M2) was approximately four times higher than the other groups at 10-year follow-up. According to the surgical margins, we found that the five-year survival rates of the R1 (marginal resection) and R2 (residual tumor) groups were similar, with the highest rate being in the R0 (wide resection) group with 78.3%. In multivariate analysis, only grade and stage had a significant association with disease-specific survival. Surgical resection combined with adjuvant radiotherapy was found to increase survival in both overall and disease-free survival of patients with dedifferentiated chondrosarcoma compared to other treatments. Conclusion: Histological subtype, grade, stage and presence of metastasis were the independent prognostic factors for survival in CS. However, marginal resection was a risk factor for local recurrence (LR), but there was no significant difference in overall survival in patients with or without LR. Although it is not significant, radiotherapy could increase survival in dedifferentiated CS variants.en_US
dc.language.isoengen_US
dc.publisherTurkish Joint Diseases Foundationen_US
dc.relation.ispartofJoint Diseases And Related Surgeryen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectChondrosarcomaen_US
dc.subjectprognostic factorsen_US
dc.subjectsurvivalen_US
dc.subjecttumoren_US
dc.titleEvaluation of prognostic factors affecting survival in chondrosarcoma treatment and comparison with literatureen_US
dc.typearticleen_US
dc.departmentAmasya Üniversitesien_US
dc.authoridCoşkun, Hüseyin Sina/0000-0003-2965-3112
dc.authoridERDOĞAN, Furkan/0000-0001-7949-1348
dc.identifier.volume33en_US
dc.identifier.issue2en_US
dc.identifier.startpage440en_US
dc.identifier.endpage448en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.52312/jdrs.2022.526
dc.department-temp[Coskun, Huseyin Sina; Erdogan, Furkan; Buyukceran, Ismail; Dabak, Nevzat] Ondokuz Mayis Univ, Fac Med, Dept Orthoped & Traumatol, Samsun, Turkeyen_US
dc.identifier.wosWOS:000828685100024en_US
dc.identifier.pmid35852206en_US
dc.authorwosidCoşkun, Hüseyin Sina/AAP-4751-2020
dc.authorwosidERDOĞAN, Furkan/HHN-1299-2022


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