Detection of MYD88 L265P mutation by next-generation deep sequencing in peripheral blood mononuclear cells of Waldenström's macroglobulinemia and IgM monoclonal gammopathy of undetermined significance.

PLoS One · 2019 · PMC6726192 · PMID 31483817

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hedged sentence

0.1900

closest p · 3.8× alpha

0.1900

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The sentences

showed a trendP = 0.19not close (p > 0.1)

Twenty-eight patients with at least minimal response showed a trend toward lower detection rate of MYD88 L265P mutation (25.0% vs. 66.7%, P = 0.19) and mutant allele burden (median, 0.00% vs. 0.22%, P = 0.07), compared to 3 patients less than minimal response.

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