PIK3CA mutations predict recurrence in localized microsatellite stable colon cancer.

PIK3 CA, which encodes the p110 α catalytic subunit of PI3K α, is one of the most frequently altered oncogenes in colon cancer ( CC), but its prognostic value is still a matter of debate. Few reports have addressed the association between PIK3 CA mutations and survival and their results are controversial. In the present study, we aimed to clarify the prognostic impact of PIK3 CA mutations in stage I-III CC according to mismatch repair status. Fresh frozen tissue samples from two independent cohorts with a total of 826 patients who underwent curative surgical resection of CC were analyzed for microsatellite instability and screened for activating point mutations in exon 9 and 20 of PIK3 CA by direct sequencing. Overall, 693 tumors (84%) exhibited microsatellite stability ( MSS) and 113 samples (14%) harbored PIK3 CA mutation. In the retrospective training cohort ( n = 433), patients with PIK3 CA-mutated MSS tumors ( n = 47) experienced a significant increased 5-year relapse-free interval compared with PIK3 CA wild-type MSS tumors ( n = 319) in univariate analysis (94% vs. 68%, Log-rank P = 0. 0003) and in multivariate analysis (HR = 0.12; 95% confidence interval, 0.029-0.48; P = 0.0027). In the prospective validation cohort ( n = 393), the favorable prognostic impact of PIK3 CA mutations in MSS tumors ( n = 327) was confirmed (83% vs. 67%, Log-rank P = 0.04). Our study showed that PIK3 CA mutations are associated with a good prognosis in patients with MSS stage I-III CC. [ABSTRACT FROM AUTHOR]