The late radiotherapy normal tissue injury phenotypes of telangiectasia, fibrosis and atrophy in breast cancer patients have distinct genotype-dependent causes.

Br J Cancer · 2007 · PMC2360097 · PMID 17325707

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hedged sentence

0.0001

closest p · 0.0× alpha

0.0001

boldest claim

The sentences

highly significantP =0.00006actually significant

The combined data ( Tables 7 and 8 ) reveal a highly significant association ( P =0.00006) with an OR of 3.06 (95% CI: 1.74–5.3) for patients carrying at least one variant allele (CT or TT) compared with the homozygous wild-type CC genotype, and therefore this increased risk applies to ∼56% (132/236) of breast cancer patients.

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