Barely Significant
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Implementation of Comprehensive Genomic Profiling in Ovarian Cancer Patients: A Retrospective Analysis.

Cancers (Basel) · 2022 · PMC9818378 · PMID 36612212

Europe PMCDOI
1
hedged sentence
0.0890
closest p · 1.8× alpha
0.0890
boldest claim

The sentences

showed a trendp = 0.089so close (0.05 < p ≤ 0.1)
Patients harboring a KRAS mutation showed a statistically significant lower OR for platinum sensitive disease (OR = 0.72 [95% CI, 0.56–0.92], p = 0.010), and patients with CCNE1 amplifications showed a trend for a statistically significant lower OR for platinum sensitive disease (OR = 0.84 [95% CI, 0.68–1.03], p = 0.089).

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