激素受体阳性/HER2 阴性乳腺癌：PIK3CA 突变状态与 PD-L1 及肿瘤细胞微环境的关联及其预后意义

Novel research data in different cancer types indicate that mutations within PIK3CA might serve as a biomarker of an improved response to immune therapy.

Therefore, the aim of this study was to evaluate and examine possible differences in the tumor microenvironment composition and PD-L1 expression as well the prognostic significance of CD4, CD8, CD68, and CD163 in PIK3CA mutated and non-mutated hormone receptor positive and HER2 negative (HR+/HER2-) breast carcinoma. Breast carcinoma tissue was analyzed by Cobas PIK3CA mutation test for the presence of PIK3CA mutation and immunohistochemistry was applied to assess PD-L1 expression and CD4, CD8, CD68, and CD163 infiltration within tumor. Statistically significant association was observed between PD-L1 expression and the presence of PIK3CA exon 20 mutation ( p = 0.

044), with PD-L1-positive patients predominantly harboring this mutation. Tumors harboring PIK3CA mutations exhibited moderate to strong statistically significant positive correlations between PD-L1 expression and infiltration by CD8 cells (rs = 0. 462, p = 0. 0027), CD68 cells (rs = 0. 398, p = 0. 0134), and CD163 cells (rs = 0. 617, p < 0. 0001).

In patients with PIK3CA mutation and exon 20 PIK3CA mutation there was statistically significant longer survival without recurrence ( p = 0. 026 and p = 0. 041, respectively). Research regarding PD-L1 expression, immune cells and PIK3CA mutations might have an impact on how to determine therapeutic approaches for patients with HR+/HER2- breast carcinoma.