Prognostic value of Ki67 expression in HR-negative breast cancer before and after neoadjuvant chemotherapy

被引:0
|
作者
Tan, Qi-Xing [1 ]
Qin, Qing-Hong [1 ]
Yang, Wei-Ping [2 ]
Mo, Qin-Guo [1 ]
Wei, Chang-Yuan [1 ]
机构
[1] Guangxi Med Univ, Tumor Hosp, Dept Breast Surg, Nanning 530021, Guangxi Provinc, Peoples R China
[2] Guangxi Med Univ, Tumor Hosp, Dept Ultrasound Diag, Nanning 530021, Guangxi Provinc, Peoples R China
关键词
Breast cancer; Ki67; neoadjuvant chemotherapy; prognosis; PATHOLOGICAL COMPLETE RESPONSE; RECEPTOR STATUS; MARKERS; TUMOR; KI-67; METAANALYSIS; CONSENSUS; SUBTYPES; THERAPY; PREDICT;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Immunohistochemical (IHC) expression of Ki67 has been identified as a prognostic and predictive marker in hormone receptor (HR)-positive breast cancer, however, there is little evidence of the association of Ki67 with prognosis in HR-negative patients. We aimed to assess the benefit of Ki67 assessment in HR-negative breast cancers after neoadjuvant chemotherapy (NAC). Methods: In the present study, a total of 183 HR-negative breast cancer patients with Stage II to III that treated with anthracycline and/or taxane-based neoadjuvant chemotherapy between 2004 and 2011 were retrospectively analyzed. Endocrine therapy and trastuzumab was not administered to any patients in this study. Clinical and pathological features of the patients with breast cancer were retrieved from the hospital records. Predictive factors for NAC response and survival were analyzed. Results: Of the 183 patients, 122 (66.6%) were HR-HER2+, and 61 (33.3%) were triple-negative. The clinical response rates were similar across breast cancer subtype. Patients whose tumors contained high Ki67 expression effectively responded to NAC. Ki67 labeling index was a predictive marker for pathologic complete response (pCR). Ki67 expression showed a positive correlation with HER2 status, tumor size, lymph node status, lymphovascular invasion and tumor grade. Furthermore, high Ki67 expression in post-treatment tumors was strongly correlated with poor disease-free survival (DFS), but no correlation of Ki-67 expression with overall survival (OS) was observed. Conclusions: Our results suggest that Ki67 expression in HR-negative breast cancer may improve the assessment of pathological response after NAC, and Ki67 score in residual tumor was an independent prognosticator for DFS in the HR-negative breast cancer patients.
引用
收藏
页码:6862 / 6870
页数:9
相关论文
共 50 条
  • [21] The prognostic value of changes in Ki67 following neoadjuvant chemotherapy in residual triple-negative breast cancer: a Swedish nationwide registry-based study
    Jenny Nyqvist-Streng
    Mikael Helou
    Khalil Helou
    Chaido Chamalidou
    Anikó Kovács
    Toshima Z. Parris
    Breast Cancer Research and Treatment, 2025, 210 (3) : 719 - 736
  • [22] Value of breast cancer molecular subtypes and Ki67 expression for the prediction of efficacy and prognosis of neoadjuvant chemotherapy in a Chinese population.
    Wang, Jiayu
    Xu, Binghe
    Sang, Die
    Zhang, Pin
    Li, Qing
    Yuan, Peng
    Ma, Fei
    Luo, Yang
    Fan, Ying
    Cai, Ruigang
    Chen, Shanshan
    Li, Qiao
    JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (15)
  • [23] Changes in Ki67 expression and clinical response to neoadjuvant chemotherapy in locally advanced breast cancer (LABC)
    Devi, Desak Gede Agung Pramesti
    Purwanto, Heru
    Sandhika, Willy
    BALI MEDICAL JOURNAL, 2021, 10 (03) : 925 - 931
  • [24] Prognostic significance of Ki67 during neoadjuvant chemotherapy in primary unresectable ovarian cancer
    Kaya, Ryusuke
    Takanashi, Hiroko
    Nakajima, Akari
    Saito, Ryosuke
    Yamaguchi, Noriko
    Morimoto, Keiji
    Isonishi, Seiji
    JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH, 2021, 47 (11) : 3979 - 3989
  • [25] Ki67 Changes Identify Worse Outcomes in Residual Breast Cancer Tumors After Neoadjuvant Chemotherapy
    Cabrera-Galeana, Paula
    Munoz-Montano, Wendy
    Lara-Medina, Fernando
    Alvarado-Miranda, Alberto
    Perez-Sanchez, Victor
    Villarreal-Garza, Cynthia
    Marisol Quintero, R.
    Porras-Reyes, Fany
    Bargallo-Rocha, Enrique
    Del Carmen, Ignacio
    Mohar, Alejandro
    Arrieta, Oscar
    ONCOLOGIST, 2018, 23 (06): : 670 - 678
  • [26] Ki67, chemotherapy response, and prognosis in breast cancer patients receiving neoadjuvant treatment
    Peter A Fasching
    Katharina Heusinger
    Lothar Haeberle
    Melitta Niklos
    Alexander Hein
    Christian M Bayer
    Claudia Rauh
    Ruediger Schulz-Wendtland
    Mayada R Bani
    Michael Schrauder
    Laura Kahmann
    Michael P Lux
    Johanna D Strehl
    Arndt Hartmann
    Arno Dimmler
    Matthias W Beckmann
    David L Wachter
    BMC Cancer, 11
  • [27] Prognostic value of Ki67 expression after short-term presurgical endocrine therapy for primary breast cancer
    Dowsett, Mitch
    Smith, Ian E.
    Ebbs, Stephen R.
    Dixon, J. Michael
    Skene, Anthony
    A'Hern, Roger
    Salter, Janine
    Detre, Simone
    Hills, Margaret
    Walsh, Geraldine
    JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2007, 99 (02): : 167 - 170
  • [28] Ki67, chemotherapy response, and prognosis in breast cancer patients receiving neoadjuvant treatment
    Fasching, Peter A.
    Heusinger, Katharina
    Haeberle, Lothar
    Niklos, Melitta
    Hein, Alexander
    Bayer, Christian M.
    Rauh, Claudia
    Schulz-Wendtland, Ruediger
    Bani, Mayada R.
    Schrauder, Michael
    Kahmann, Laura
    Lux, Michael P.
    Strehl, Johanna D.
    Hartmann, Arndt
    Dimmler, Arno
    Beckmann, Matthias W.
    Wachter, David L.
    BMC CANCER, 2011, 11
  • [29] The prognostic significance of Ki-67 expression before and after neoadjuvant anthracycline-taxane-based chemotherapy in different biological breast cancer phenotypes
    Zhang, J.
    Zhang, X.
    Yu, F.
    Liu, J.
    Zhang, S.
    Hao, X.
    Hou, G.
    CANCER RESEARCH, 2013, 73
  • [30] Prognostic value of Ki67 analysed by cytology or histology in primary breast cancer
    Robertson, Stephanie
    Stalhammar, Gustav
    Darai-Ramqvist, Eva
    Rantalainen, Mattias
    Tobin, Nicholas P.
    Bergh, Jonas
    Hartman, Johan
    JOURNAL OF CLINICAL PATHOLOGY, 2018, 71 (09) : 787 - 794