Risk stratification in luminal-type breast cancer: Comparison of Ki-67 with EndoPredict test results

被引:13
|
作者
Noske, Aurelia [1 ]
Anders, Sophie-Isabelle [2 ]
Ettl, Johannes [2 ]
Hapfelmeier, Alexander [3 ]
Steiger, Katja [1 ]
Specht, Katja [1 ]
Weichert, Wilko [1 ]
Kiechle, Marion [2 ]
Klein, Evelyn [2 ]
机构
[1] Tech Univ Munich, Sch Med, Inst Pathol, Munich, Germany
[2] Tech Univ Munich, Dept Obstet & Gynecol, Klinikum Rechts Isar, Munich, Germany
[3] Tech Univ Munich, Inst Med Stat & Epidemiol, Klinikum Rechts Isar, Munich, Germany
来源
BREAST | 2020年 / 49卷
关键词
Breast cancer; Luminal-type; Risk stratification; EndoPredict; Ki-67; INTERNATIONAL EXPERT CONSENSUS; 21-GENE RECURRENCE SCORE; LATE DISTANT RECURRENCE; PRIMARY THERAPY; PAM50; RISK; KI67; HIGHLIGHTS; RECOMMENDATIONS; INFORMATION; STRATEGIES;
D O I
10.1016/j.breast.2019.11.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: Adjuvant chemotherapy decision in patients with hormone receptor positive, HER2 negative breast cancer (BC) is challenging. Ki-67 is widely used for adjuvant therapy decision in BC. The multigene assay EndoPredict (EP) has shown to provide valid and additional information about the risk of recurrence compared to traditional pathological factors. In this study, we compared Ki-67 with EP assay generated risk groups. Methods: We analyzed the results from prospective EP testing (n = 373) and tumor proliferation assessed by Ki-67 staining in luminal breast cancer. We statistically investigated the association of both parameters and probed for equivalence in risk stratification. Results: Evaluation of Ki-67 was feasible in 307 (82%) BC specimens with known EP test results. The EPscore (now called 12-gene molecular score) delineated 140 low and 167 high scores. After combining the EPscore with pathological tumor stage and nodal status, we received 203 EPclin low-risk and 104 EPclin high-risk classifications. EPscore and EPclin were significantly associated with Ki-67 indices and tumor grade (p < 0.001). Overall, we observed a moderate correlation between Ki-67 and the EPscore (r = 0.63) as well as the EPclin score (r = 0.59). Conclusion: Ki-67 values above 25% partly overlap with EP test results and therefore indicate a high-risk profile. In these cases, the additional prognostic information from EP testing might be rather low. However, low and intermediate Ki-67 values (less than 25%) alone were not reliable in predicting a low risk EP profile, indicating that EP testing is useful in this subgroup. (C) 2019 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:101 / 107
页数:7
相关论文
共 50 条
  • [41] Whole genome sequencing to characterize luminal-type breast cancer
    Ellis, Matthew James
    Ding, Li
    Shen, Dong
    Luo, Jingqin
    Suman, Vera J.
    Goiffon, Reece J.
    Wallis, John W.
    Goldstein, Theodore C.
    Chen, Ken
    Allred, Donald Craig
    Leitch, A. Marilyn
    Olson, John A.
    Ota, David M.
    Watson, Mark
    Piwnica-Worms, David
    Bose, Ron
    Stuart, Joshua M.
    Wilson, Richard K.
    Hunt, Kelly
    Mardis, Elaine
    JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (15)
  • [43] KI-67 ANTIBODIES (KI-S5, MIB-1, AND KI-67) IN BREAST CARCINOMAS - A BRIEF QUANTITATIVE COMPARISON
    MAURI, FA
    GIRLANDO, S
    DALLAPALMA, P
    BUFFA, G
    PERRONE, G
    DOGLIONI, C
    KREIPE, H
    BARBARESCHI, M
    APPLIED IMMUNOHISTOCHEMISTRY, 1994, 2 (03): : 171 - 176
  • [44] Ki-67 is a Luminal B marker that identifies a high-risk subgroup in hormone receptor positive and node negative breast cancer
    Cheang, M.
    Voduc, D.
    Leung, S.
    Turbin, D.
    Bernard, P. S.
    Ellis, M.
    Mardis, E.
    Perou, C. M.
    Nielsen, T. O.
    JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (18)
  • [45] Visual and digital assessment of Ki-67 in breast cancer tissue-a comparison of methods
    Skjervold, Anette H.
    Pettersen, Henrik Sahlin
    Valla, Marit
    Opdahl, Signe
    Bofin, Anna M.
    DIAGNOSTIC PATHOLOGY, 2022, 17 (01)
  • [46] Ki-67 is an independent indicator in non-muscle invasive bladder cancer (NMIBC); Combination of EORTC risk scores and Ki-67 expression could improve the risk stratification of NMIBC
    Ding Weihong
    Gou, Yuancheng
    Sun, Chuanyu
    Xia, Guowei
    Wang, Hong
    Chen, Zhongqing
    Tan, Jun
    Xu, Ke
    Ding, Qiang
    UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2014, 32 (01) : 42.e13 - 42.e19
  • [47] A comparative study of Ki-67 antigen expression between luminal A and triple-negative subtypes of breast cancer
    Borges, Umbelina Soares
    Costa-Silva, Danylo Rafhael
    da Silva-Sampaio, Joao Paulo
    Escorcio-Dourado, Carla Solange
    Conde, Airton Mendes, Jr.
    Campelo, Viriato
    Gebrim, Luiz Henrique
    da Silva, Benedito Borges
    Lopes-Costa, Pedro Vitor
    MEDICAL ONCOLOGY, 2017, 34 (09)
  • [48] Proliferative activity in human breast cancer: Ki-67 automated evaluation and the influence of different Ki-67 equivalent antibodies
    Fasanella, S.
    Leonardi, E.
    Cantaloni, C.
    Eccher, C.
    Bazzanella, I.
    Aldovini, D.
    Bragantini, E.
    Morelli, L.
    Cuorvo, L. V.
    Ferro, A.
    Gasperetti, F.
    Berlanda, G.
    Dalla Palma, P.
    Barbareschi, M.
    DIAGNOSTIC PATHOLOGY, 2011, 6
  • [49] A comparative study of Ki-67 antigen expression between luminal A and triple-negative subtypes of breast cancer
    Umbelina Soares Borges
    Danylo Rafhael Costa-Silva
    João Paulo da Silva-Sampaio
    Carla Solange Escórcio-Dourado
    Airton Mendes Conde
    Viriato Campelo
    Luiz Henrique Gebrim
    Benedito Borges da Silva
    Pedro Vitor Lopes-Costa
    Medical Oncology, 2017, 34
  • [50] Differences in Stemness Properties Associated With the Heterogeneity of Luminal-Type Breast Cancer
    Ito, Takako
    Sato, Nozomi
    Yamaguchi, Yuri
    Tazawa, Chika
    Moriya, Takuya
    Hirakawa, Hisashi
    Hayashi, Shin-ichi
    CLINICAL BREAST CANCER, 2015, 15 (02) : E93 - E103