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Also predefined sensitivity analyses confirmed our primary efficacy result.
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Secondary efficacy measures confirmed primary efficacy results.
Analyses run on the PP population confirmed the primary efficacy results.
Primary efficacy results are also presented for each study separately.
The primary efficacy results for the ITT population were similar.
Baseline characteristics and primary efficacy results have been reported previously [ 6– 8].
Primary efficacy results were analyzed using Pearson's Chi-square test.
Post hoc sensitivity analyses of the primary efficacy endpoint were consistent with the primary efficacy results (ESM Table 2).
The demographics, primary efficacy results and safety findings of the STAR study have been presented in detail elsewhere [ 18].
Summary of primary efficacy results: smoking cessation and smoking reduction from week 6 to month 4, and from month 6 to month 12.
As this was time-driven rather than an event-driven analysis, the primary efficacy results may have been affected by the high rates of discontinuation while on tamoxifen monotherapy and the timing of the exemestane switch [ 39].
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