4.4 Article

PIK3CA Mutation as Potential Poor Prognostic Marker in Asian Female Breast Cancer Patients Who Received Adjuvant Chemotherapy

Journal

CURRENT ONCOLOGY
Volume 29, Issue 5, Pages 2895-2908

Publisher

MDPI
DOI: 10.3390/curroncol29050236

Keywords

PIK3CA mutation; adjuvant chemotherapy; breast cancer; invasive ductal carcinoma; c-Met; PD-L1; microsatellite instability; mismatch repair proteins

Categories

Funding

  1. National Research Foundation of Korea - Korean Ministry of Science and I.C.T. [NRF-2019R1C1C1004463, NRF-2021R1G1A1093593]

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This study investigates the prognostic relevance of the PIK3CA mutation along with PD-L1, c-Met, and mismatch repair deficiency (dMMR) in Asian women with breast cancer. The results suggest that the PIK3CA mutation, along with c-Met positivity or dMMR/MSI status, may be associated with poor prognosis in breast cancer, especially in Asian women.
Background: The prognostic relevance of the PIK3CA mutation together with PD-L1, c-Met, and mismatch repair deficiency (dMMR) have not been fully investigated in Asian women with breast cancer (BC) who have undergone postoperative adjuvant chemotherapy. Methods: We analyzed PIK3CA mutations via peptide nucleic acid (PNA)-mediated real-time PCR assay, PD-L1/c-Met expression via immunohistochemistry (IHC), and microsatellite instability (MSI) status using PCR and IHC, in 191 resected BCs from 2008 to 2011. The Cancer Genome Atlas (TCGA) dataset for the involvement of the PIK3CA mutation with PD-L1/c-Met/MMR was explored. Results: The PNA clamp-mediated assay was able to detect the PIK3CA mutation in 1% of the mutant population in the cell line validation. Using this method, the PIK3CA mutation was found in 78 (49.4%) of 158 samples. c-Met and PD-L1 positivity were identified in 31.4 and 21.8% of samples, respectively, which commonly correlated with high histologic grade and triple-negative subtype. MSI/dMMR was observed in 8.4% of patients, with inconsistency between MMR IHC and the MSI PCR. The PIK3CA mutation exhibited a poor prognostic association regarding recurrence-free survival (RFS) in both overall and triple-negative BCs. In subgroup analyses, the PIK3CA-mutated tumors showed poorer RFS than the PIK3CA-wildtype within the c-Met-positive, MSS, triple-negative, or age onset <50 years subgroups, which showed a similar trend of association in TCGA data. Conclusions: PIK3CA mutation together with c-Met or dMMR/MSI status might be relevant to poor prognosis in BC subsets, especially in Asian women.

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