Differences in prognosis and efficacy of chemotherapy by p53 expression in triple-negative breast cancer
Autor: | Seung Pil Jung, Soo Youn Bae, Seok Jin Nam, Yong Sik Jung, Hsien Wen Yang, Sae Byul Lee, Byung Woo Park, Sung Hoo Jung, Woosung Lim |
---|---|
Rok vydání: | 2018 |
Předmět: |
Adult
0301 basic medicine Oncology Cancer Research medicine.medical_specialty medicine.medical_treatment Triple Negative Breast Neoplasms Disease-Free Survival 03 medical and health sciences 0302 clinical medicine Breast cancer Internal medicine Biomarkers Tumor medicine Humans Stage (cooking) P53 expression Triple-negative breast cancer Aged Chemotherapy Univariate analysis business.industry Immunochemical staining Middle Aged Prognosis medicine.disease 030104 developmental biology Chemotherapy Adjuvant 030220 oncology & carcinogenesis Mutation Immunohistochemistry Female Tumor Suppressor Protein p53 business |
Zdroj: | Breast Cancer Research and Treatment. 172:437-444 |
ISSN: | 1573-7217 0167-6806 |
DOI: | 10.1007/s10549-018-4928-2 |
Popis: | TP53 mutation is the most common mutation in breast cancer, and it is considered a target marker of triple-negative breast cancer (TNBC). We investigated whether expression of p53 detected by immunochemical staining predicts the chemotherapy response of TNBC. A total of 11,393 TNBC patients who had between stage I and stage III enrolled in the Korean Breast Cancer Society Registry database from January 1, 2000 to December 31, 2015. There were 6,331 ‘p53-positive (+) TNBC’ patients and 5062 ‘p53-negative (−) TNBC’ patients. In univariate analysis, p53(+) TNBC had a worse prognosis than p53(−) TNBC in patients not receiving chemotherapy (P = 0.003). However, there was no difference in prognosis between p53(+) TNBC and p53(−) TNBC for patients receiving chemotherapy. In multivariate analysis adjusted for age and stage, the risk of p53(+) TNBC was 1.84 times higher than that of p53(−) TNBC in the non-chemotherapy group. However, there was no difference between p53(+) TNBC and p53(−) TNBC in patients receiving chemotherapy. In p53(+) TNBC, the risk was 0.6-fold lower when chemotherapy was administered than when chemotherapy was not administered. However, in p53(−) TNBC, there was no risk reduction effect by chemotherapy. The prognosis of p53(+) TNBC has worse than p53(−) TNBC, but the risk for survival was significantly reduced with chemotherapy. It suggests that p53(+) TNBC would be more sensitive to chemotherapy than p53(−) TNBC. |
Databáze: | OpenAIRE |
Externí odkaz: |