Oct 2026· Journal of the Formosan Medical Association = Taiwan yi zhi· 1 citation· 21 references
Medicine
Abstract
Background
While Western literature identifies age, histological grade, tumor characteristics, and metastasis as key prognostic factors for chondrosarcoma survival, data specifically focusing on the Taiwanese population remain sparse.
Methods
This retrospective study included patients who were pathologically diagnosed with chondrosarcoma between January 1998 and July 2016. Clinical and demographic variables were collected, including sex, age, tumor characteristics (size, anatomical location, histological subtype, and pathological grade), treatment modalities (surgical approach and adjuvant therapies), and disease status within a five-year interval following diagnosis. Cox proportional hazards and logistic regression models were utilized to evaluate prognostic factors and to construct a predictive model.
Results
Among 58 patients (mean age 47.4 ± 18.3 years; 5-year OS 77.6%), multivariate Cox regression showed that advanced age, progressive systemic disease (aHR 10.07, 95% CI: 1.49-68.00; p < 0.05), and primary metastatic disease (aHR 11.03, 95% CI: 1.62-75.20; p < 0.05) independently predicted worse survival. The multivariate logistic regression model demonstrated high discriminative ability (AUC = 0.954), supporting the use of the derived nomogram for individualized prognosis.
Conclusion
This study identifies advanced age and unfavorable disease status as independent negative predictors of 5-year survival in chondrosarcoma. The developed prognostic model and nomogram demonstrated high predictive accuracy, providing a robust tool for clinical risk stratification and personalized management of this patient population.
This real-world CUP cohort shows patients with favorable risk groups have better survival outcomes than unfavorable risk groups, with survival comparable to specialized international series.
L. Thongthieang· Journal of the Medical Assoc...· 0 citations
Background: Leiomyosarcoma (LMS) is a rare aggressive sarcoma with substantial heterogeneity in anatomical presentation, stage, treatment, and survival. We evaluated clinical characteristics, treatment patterns, and survival, with particular emphasis on whether anatomical site independently predicted overall survival (...
R. Pinninti, K. Subramaniyan, R. Iyer et al.· Journal of Clinical Medicine· 0 citations
Introduction/Objective. The objective was to evaluate inflammatory composite indicators and clinical features as prognostic factors and develop a predictive model for glioma malignancy grade. Methods. A retrospective analysis of 107 patients with glioma who underwent surgical resection was conducted. Clinical data, inc...
Bing-Heng Wang, Yong-Chang He· Srpski Arhiv za Celokupno Le...· 0 citations
Findings provide real-world evidence to guide clinical management of these rare malignancies and show complete resection remains the cornerstone of survival in TETs.
E. Turkoğlu, D. Işık, Nisanur Sarıyar Busery et al.· Cerrahpasa Medical Journal· 0 citations
AIM
To evaluate postoperative progression-free survival (PFS), identify clinicopathological factors associated with PFS, and explore the association between postoperative adjuvant therapy and PFS after surgery for urachal carcinoma.
METHODS
We retrospectively included 72 patients with histopathologically confirmed ma...
Hong-Yu Zhang, Ze-Xuan Lv, Zi-Jian Wang et al.· Urologic oncology· 0 citations
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