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Exact(27)
No other differences in recurrence sites with adjuvant trastuzumab were observed (Table 3; Additional files 8, 9, Tables S8, S9).
When the two internal cohorts were combined (n = 431, median follow-up = 36 months) the differences in recurrence rates became more statistically significant (P <0.001).
Kaplan-Meier analysis and log rank tests were used to illustrate differences in recurrence free survival (RFS), breast cancer specific survival (BCSS) and overall survival (OS) according to CD163 and CD68 expression.
Due to the insufficient power, the RCTs [18, 36, 64, 65], which were conducted in this indication could not show any statistical differences in recurrence rates between different RFA and surgery.
Among the triptans there are only minor, but sometimes statistically significant differences in recurrence and sustained pain-free responses [8, 21].
Later, in 2002, Chen et al. [33] compared the recurrences after percutaneous biopsies vs surgical biopsies in patients with breast-conserving therapy, and found no significant differences in recurrence rates.
Similar(33)
There is also no difference in recurrence free survival or overall survival.
Similar to FISH, we observed no difference in recurrence free survival between patients with negative cytology and positive or negative immunocytology in our study.
For patients achieving a pCR, there was no difference in recurrence between patients who received chemoradiotherapy vs chemotherapy alone (26%and15%5%, respectively, P=0.2).
Possible other explanations for the difference in recurrences rates between the different studies are heterogeneity of data collection and selection bias, for instance excluding women with a stage 4 uterine descent.
Meanwhile, some differences were found in recurrence patterns and prognostic factors between GB cancer and BDC.
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