Journal of the National Cancer Institute, volume 113, issue 7, pages 808-819

Assessment of Ki67 in Breast Cancer: Updated Recommendations From the International Ki67 in Breast Cancer Working Group

TORSTEN TOFTEGAARD NIELSEN 1
Samuel Leung 1
A. R. Dodson 3
Balazs Acs 4, 5
M. Ellis 8
Susan Fineberg 9
MARGARET FLOWERS 10
Hans Kreipe 11
Anne-Vibeke Laenkholm 12
Hongchao Pan 13
Frédérique Penault-Llorca 14
Mei-Yin Polley 15
Roberto B. Salgado 16, 17
Ian E. Smith 18
Tomoharu Sugie 19
John M.S. Bartlett 20, 21
L. McShane 22
M. Dowsett 23
Daniel Hayes 24
Show full list: 22 authors
3
 
The UK National External Quality Assessment Scheme for Immunocytochemistry and In-Situ Hybridisation, London, UK
5
 
Department of Clinical Pathology and Cytology, Karolinska University Laboratory, Stockholm, Sweden
10
 
Breast Cancer Research Foundation, New York, NY, USA
11
 
Medical School Hannover, Institute of Pathology, Hannover, Germany
16
 
Department of Pathology, GasthuisZusters Antwerpen / Hospital Network Antwerp (GZA-ZNA), Antwerp, Belgium
18
 
Breast Unit, Royal Marsden Hospital, London, UK
23
 
Breast Cancer Now Toby Robins Research Centre, Institute of Cancer Research, London, UK
Publication typeJournal Article
Publication date2020-12-28
scimago Q1
SJR4.986
CiteScore17.0
Impact factor9.9
ISSN00278874, 14602105
PubMed ID:  33369635
Cancer Research
Oncology
Abstract

Ki67 immunohistochemistry (IHC), commonly used as a proliferation marker in breast cancer, has limited value for treatment decisions due to questionable analytical validity. The International Ki67 in Breast Cancer Working Group (IKWG) consensus meeting, held in October 2019, assessed the current evidence for Ki67 IHC analytical validity and clinical utility in breast cancer, including the series of scoring studies the IKWG conducted on centrally stained tissues. Consensus observations and recommendations are: 1) as for estrogen receptor and HER2 testing, preanalytical handling considerations are critical; 2) a standardized visual scoring method has been established and is recommended for adoption; 3) participation in and evaluation of quality assurance and quality control programs is recommended to maintain analytical validity; and 4) the IKWG accepted that Ki67 IHC as a prognostic marker in breast cancer has clinical validity but concluded that clinical utility is evident only for prognosis estimation in anatomically favorable estrogen receptor–positive and HER2-negative patients to identify those who do not need adjuvant chemotherapy. In this T1-2, N0-1 patient group, the IKWG consensus is that Ki67 5% or less, or 30% or more, can be used to estimate prognosis. In conclusion, analytical validity of Ki67 IHC can be reached with careful attention to preanalytical issues and calibrated standardized visual scoring. Currently, clinical utility of Ki67 IHC in breast cancer care remains limited to prognosis assessment in stage I or II breast cancer. Further development of automated scoring might help to overcome some current limitations.

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