The Prognostic Impact of Tumor Size and BRAF Mutational Status in Middle Eastern Differentiated Thyroid Cancer.

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Tác giả: Fouad Al-Dayel, Khawla S Al-Kuraya, Maha Al-Rasheed, Saif S Al-Sobhi, Wael Haqawi, Sandeep Kumar Parvathareddy, Zeeshan Qadri, Abdul K Siraj, Nabil Siraj

Ngôn ngữ: eng

Ký hiệu phân loại: 332.6042 Investment

Thông tin xuất bản: United States : The Journal of clinical endocrinology and metabolism , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 751027

 CONTEXT: Tumor size at diagnosis has been widely used as a major mortality risk factor in risk stratification of differentiated thyroid cancer (DTC). OBJECTIVE: The current study was designed to analyze whether tumor size at diagnosis is a major prognostic factor in Middle Eastern DTC. METHODS: We conducted a comparative study of the relationship between tumor size at diagnosis and event-free survival (EFS) with respect to BRAF status in 1709 consecutive patients treated surgically for DTC. Patients were divided into 4 groups according to the size of tumor and BRAF mutation status: Group 1 (≤4 cm without BRAF mutation), Group 2 (≤4 cm with BRAF mutation), Group 3 (>
 4 cm without BRAF mutation), and Group 4 (>
 4 cm with BRAF mutation). Predictors of EFS were compared using the log-rank test and Cox proportional hazards models. RESULTS: Tumor size >
 4 cm was associated with clinicopathologic characteristics, such as older age, male gender, bilateral tumors, extrathyroidal extension, lymphovascular invasion, advanced tumor stage, and persistent/recurrent disease. Tumor size was also inversely associated with BRAF mutation. Both tumor size (>
 4 cm) and BRAF mutation were associated with EFS on univariate analysis. On subgroup analysis, larger tumor size was an independent predictor of EFS (Group 3 vs Group 1), irrespective of BRAF mutation status. Also, within the BRAF mutant tumors, larger tumor size was still an independent predictor of EFS (Group 4 vs Group 2). CONCLUSION: Tumor size is an independent predictor of EFS in Middle Eastern patients with DTC, regardless of BRAF mutational status.
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