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. Oncologic resection achieving r0 margins improves disease-free survival in parathyroid cancer . Annals of Surgical Oncology 2014 21 1891 – 1897 . ( https://doi.org/10.1245/s10434-014-3530-z ) 12 Marcocci C Cetani F . Clinical practice. Primary
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predictor for disease-free survival (DFS) in patients with stage III or IV papillary thyroid cancer ( 30 ). Lee et al. reported that preoperative NLR for papillary thyroid cancer in patients aged ≥ 45 years is an independent predictor of DFS ( 31 ). In a
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have a favorable prognosis, with a 10-year survival rate of PTC patients up to 95% ( 4 ). However, the recurrence rate of PTC with locoregional lymph node metastases varies from 4% to 32% ( 5 ). PTC recurrence significantly impacts quality of life, with
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-medullary thyroid cancer patients expressing PD-L1 were three times more likely to have a poorer disease-free survival (DFS) than patients who did not have positive PD-L1 expression ( 12 ). Immunotherapies targeting the PD-1/PD-L1 pathway have demonstrated durable
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, the mean Ki-67 index was 51 ± 22, ranging from 20 to 100. To determine the clinical relationship between the Ki-67 index and OS, progression free survival (PFS) in rectal NECs, the scatter diagram of OS, PFS and Ki-67 distribution were developed using
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, NRAS and TERT p status, additional treatments, disease-free status at one year, disease-free status at the end of follow-up or disease-specific survival in the DTC group. When we analyzed NIS expression between WT PTCs and those harboring any of the
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Cancer staging system, and disease-free survival (DFS) were evaluated. Statistical analysis We used R (version 3.5.1, R Foundation for Statistical Computing, Vienna, Austria; https://www.r-project.org/ ) for statistical analysis. Continuous
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prognostic factor for survival (4, 5) . However, the presence of CLNM has been shown to increase local recurrence rates (6, 7) to up to 31% of patients (8) . There is an ongoing debate about the role of systematic central lymph node (LN) dissection in PTC
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relationship with the clinical-pathological parameters and the analysis of the association between concentration of the marker and progression free survival (PFS) and overall survival (OS). Materials and methods We analysed retrospectively the data of
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( 36 ). Statistical analysis Contingency table analysis and Chi square tests were used to study the relationship between clinicopathological variables and protein expression. Disease-free survival curves were generated using the Kaplan