Impact on survival of estrogen receptor, progesterone receptor and Ki-67 expression discordance pre- and post-neoadjuvant chemotherapy in breast cancer

• Published in: PloS one 2020-04, Vol.15 (4), p.e0231895-e0231895
• Main Authors: Ding, Yuqin, Ding, Kaijing, Qian, Hongdan, Yu, Xingfei, Zou, Dehong, Yang, Hongjian, Mo, Wenju, He, Xiangming, Zhang, Fanrong, Qin, Chengdong, Zheng, Yurong, Ding, Xiaowen
• Format: Article
• Language: English
• Subjects: Biology and Life Sciences; Biomarkers; Breast cancer; Cancer therapies; Chemotherapy; Discordance; Endocrine therapy; Estrogen receptors; Estrogens; Hospitals; Immunohistochemistry; Mammography; Medical prognosis; Medical research; Medicine and Health Sciences; Patients; Progesterone; Prognosis; Receptors; Studies; Surgery; Survival; Tumors
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0231895

To investigate whether estrogen receptor (ER), progesterone receptor (PR) and Ki-67 expression discordance before and after neoadjuvant chemotherapy (NAC) correlates with prognosis and treatment of breast cancer patients. The study cohort included 482 breast cancer patients at the Zhejiang Cancer Hospital from January 1, 2008, to December 31, 2018. Core needle biopsies and excised tissue biopsies pre- and post-NAC were obtained. Immunohistochemistry was used to determine ER, PR and Ki-67 status. The relationship between biomarker discordance before and after NAC and clinicopathological features was compared retrospectively. ER (n = 482), PR (n = 482) and Ki-67 (n = 448) expression was assessed in the same lesion pre- and post-NAC. Discordance in the three markers pre- and post-NAC was observed in 50 (10.4%), 82 (17.0%) and 373 (77.4%) cases, respectively. Positive-to-negative PR expression changes were the most common type of discordance observed. The risk of death in patients with a PR positive-to-negative conversion was 6.58 times greater than for patients with stable PR expression. The risk of death in patients with increased Ki-67 expression following NAC treatment was 2.05 times greater than for patients with stable Ki-67 expression. Breast cancer patients showed changes in ER, PR and/or Ki-67 status throughout NAC, and these changes possibly influenced disease-free survival and overall survival. A switch to negative hormone receptor expression with increased Ki-67 expression following NAC could be indicators of a worse prognosis. Biomarker expression investigations following NAC may potentially improve patient management and survival.