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Zhang, Chenxin

https://orcid.org/0009-0006-3569-0250

Mayo Clinic

Albert Einstein College of Medicine

Citations 1

p16, COX-2, and Ki67 Protein Expression in DCIS and Risk of Ipsilateral Invasive Breast Cancer
Rohan, Thomas E. , Zhang, Chenxin , Wang, Yihong , Couch, Fergus J. , Greenlee, Robert T. , Honda, Stacey , Stark, Azadeh , White, Larissa L. , Chitale, Dhananjay , Xue, Xiaonan , Ginsberg, Mindy , Loudig, Olivier , Wang, Yihong , Couch, Fergus J. , Chitale, Dhananjay A , Loudig, Olivier

Cancer Epidemiology, Biomarkers & Prevention | April 14, 2025 | Volume: 34 | Issue: 6 | Pages: 1036-1039

10.1158/1055-9965.epi-25-0143 Get It

Abstract Background: Prior research on the associations of p16, COX-2, and Ki67 immunopositivity in ductal carcinoma in situ (DCIS) tissue with the risk of subsequent ipsilateral invasive breast cancer (IBC) is limited. Methods: In a case–control study nested in a cohort of women diagnosed with DCIS, immunostaining for p16, COX-2, and Ki67 was performed on DCIS tissue from those who developed subsequent ipsilateral IBC (cases; n = 146) and on matched subjects who did not develop IBC (controls; n = 273). Conditional logistic regression was used to estimate ORs and 95% confidence intervals for the associations between immunopositivity for p16, COX-2, and Ki67 and the risk of subsequent ipsilateral IBC. Results: There was no association between p16, COX-2, and Ki67 immunopositivity, examined either individually or in combination, and a risk of ipsilateral IBC. Compared with all other groups, the multivariable OR (95% confidence interval) for women who were triple positive for the three markers was 1.16 (0.38–3.54). Conclusions: p16, COX-2, and Ki67 immunopositivity was not associated with altered risk of ipsilateral IBC in women with DCIS. Impact: p16, COX-2, and Ki67 may not be prognostic for ipsilateral IBC in women with DCIS.