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progression-free interval (PFI) (HR = 0.89, 95% CI: 0.52–1.52, P = 0.680), although the difference between the two survival curves was not significant ( Fig. 3B ). Figure 3 Overall survival curve (A) and progression-free interval curve (B) of patients
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patients could have CCLNM. The outcome of this study is based on soft data (e.g., the presence or absence of metastases in the contralateral central lymph nodes), but not on the recurrence rate or survival. Age is an important prognostic factor for DTC
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uptake in bone lesions may still benefit from it ( 12 ). At present, studies of DTC patients with bone metastases treated with I-131 have focused on evaluating overall survival and have largely failed to assess the locoregional progression-free survival
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.d. were used to express normally distributed data (such as the age of the patients) and median with interquartile range (IQR) were used for non-normally distributed data (such as the tumor size and the follow-up). The disease-free survival (DFS) and the
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-year progression-free survival (PFS) (SD or partial response (PR) according to RECISTv1.1). Patients with PR were grouped together with patients with SD in all analyses (SD group). In patients who underwent multiple systemic treatments during follow
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early recurrence in breast cancer ( 23 ). However, another report shows an association between the expression of DDX1 with improved local relapse-free-, distant metastasis-free- and overall survival in patients diagnosed with early stage node-negative BC
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600E + TERT promoter Co-occurrence of BRAF V600E and TERT c.-124C>T mutations associate with decreased recurrence-free survival of PTC patients Song et al. 2016 ( 16 ) PTC + FTC 551 BRAF V600E + TERT promoter; RAS + TERT
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were used to calculate the LRFS (local relapse-free survival), DDFS (distant disease-free survival), OS (overall survival) and PFS (progression-free survival). Kaplan–Meier survival analysis and log-rank test were utilized to compare the survival
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. It is hoped that early detection of persistent or recurrent disease will improve disease-free survival ( 7 ). Uptake of 131 I into thyroid tissue is a prerequisite for remnant ablation. 131 I is predominantly a beta emitter which provides the
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associations between the status of ATF2/p-ATF2/p-ERK expression in non-muscle-invasive tumors and a recurrence-free survival or progression-free survival (PFS) rate as well as between that of ATF2 expression in muscle-invasive tumors and a PFS or cancer