Systematically higher Ki67 scores on core biopsy samples compared to corresponding resection specimen in breast cancer: a multi-operator and multi-institutional study

  • Breast Int Grp
  • , North Amer Breast Canc Grp BIG-NAB
  • , Balazs Acs*
  • , Samuel C. Y. Leung
  • , Kelley M. Kidwell
  • , Indu Arun
  • , Renaldas Augulis
  • , Sunil S. Badve
  • , Yalai Bai
  • , Anita L. Bane
  • , John M. S. Bartlett
  • , Jane Bayani
  • , Gilbert Bigras
  • , Annika Blank
  • , Henk Buikema
  • , Martin C. Chang
  • , Robin L. Dietz
  • , Andrew Dodson
  • , Susan Fineberg
  • , Cornelia M. Focke
  • Dongxia Gao, Allen M. Gown, Carolina Gutierrez, Johan Hartman, Zuzana Kos, Anne-Vibeke Laenkholm, Arvydas Laurinavicius, Richard M. Levenson, Rustin Mahboubi-Ardakani, Mauro G. Mastropasqua, Sharon Nofech-Mozes, C. Kent Osborne, Frederique M. Penault-Llorca, Tammy Piper, Mary Anne Quintayo, Tilman T. Rau, Stefan Reinhard, Stephanie Robertson, Roberto Salgado, Tomoharu Sugie, Bert van der Vegt, Giuseppe Viale, Lila A. Zabaglo, Daniel F. Hayes, Mitch Dowsett, Torsten O. Nielsen, David L. Rimm
*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    34 Citations (Scopus)
    132 Downloads (Pure)

    Abstract

    Ki67 has potential clinical importance in breast cancer but has yet to see broad acceptance due to inter-laboratory variability. Here we tested an open source and calibrated automated digital image analysis (DIA) platform to: (i) investigate the comparability of Ki67 measurement across corresponding core biopsy and resection specimen cases, and (ii) assess section to section differences in Ki67 scoring. Two sets of 60 previously stained slides containing 30 core-cut biopsy and 30 corresponding resection specimens from 30 estrogen receptor-positive breast cancer patients were sent to 17 participating labs for automated assessment of average Ki67 expression. The blocks were centrally cut and immunohistochemically (IHC) stained for Ki67 (MIB-1 antibody). The QuPath platform was used to evaluate tumoral Ki67 expression. Calibration of the DIA method was performed as in published studies. A guideline for building an automated Ki67 scoring algorithm was sent to participating labs. Very high correlation and no systematic error (p = 0.08) was found between consecutive Ki67 IHC sections. Ki67 scores were higher for core biopsy slides compared to paired whole sections from resections (p

    Original languageEnglish
    Pages (from-to)1362–1369
    Number of pages8
    JournalModern Pathology
    Early online date21-Jun-2022
    DOIs
    Publication statusPublished - 2022

    Keywords

    • DIGITAL-IMAGE-ANALYSIS
    • KI-67 LABELING INDEX
    • NEEDLE BIOPSIES
    • BIOMARKER ASSESSMENT
    • INTERNATIONAL KI67
    • MULTICENTER
    • IMMUNOHISTOCHEMISTRY
    • REPRODUCIBILITY
    • PROLIFERATION
    • RELIABILITY

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