Median (range) progression-free survival in the first line after MP was 8.2 months (1.4 49.5+).
Studies on evolution of HSIL during pregnancy and the post-partum period show a range of progression to micro-invasive carcinoma from 0 to 14.2 % and a very low risk of progression to frankly invasive cancer (0.1 %) (reviewed in Serati et al., [ 44]).
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During a median follow-up period of 5.9 years (range 0.3 8.6), progression of albuminuria was observed in 85 patients.
The present results show a wide range of progression rates, and a wide range of ages at which MIN and invasive cancers were first detected.
The range and progression of exercises is well set-out in clinical texts [ 28] and is individualised to the patient based on this presentation.
In contrast to the change in individual ALSFRS-R scores between assessments (Supplementary Fig. 2B), there was notably limited individual variability across a range of progression rates (Supplementary Fig. 2C).
This training series included patients with more advanced NSCLC (Stage IIIB) in order to capture a broad range of progression-related genomic information.
Several groups also reported prolonged time to progression (range, 7.6 21.7 months) and OS time (range, 13.0 30.5 months) in patients with EGFR mutations (Chou et al, 2005; Cortes-Funes et al, 2005; Han et al, 2005; Kim et al, 2005; Mitsudomi et al, 2005; Takano et al, 2005; Taron et al, 2005; Zhang et al, 2005).
The ratios β (progression range since the beginning of the event) and β' (present progression range) were calculated to describe the improvement over the final time frame in each event by using the following equation: β = (BPi/b)×100 and β' = (BPf/b)×100.
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