How Reliable Is Ki-67 Immunohistochemistry in Grade 2 Breast Carcinomas? A QA Study of the Swiss Working Group of Breast- and Gynecopathologists

Zsuzsanna Varga(University of Zurich), Joachim Diebold(Luzerner Kantonsspital), Corina Dommann‐Scherrer(Kantonsspital Winterthur), Harald Frick(Kantonsspital Graubünden), Daniela Kaup(Mittal hospital), Aurelia Noske(University of Zurich), Ellen C. Obermann(University of Basel), Christian Öhlschlegel(University of St.Gallen), Barbara Padberg(Kantonsspital Graubünden), Christiane Rakozy(AC Diagnostics (United States)), Sara Sancho Oliver, Sylviane Schobinger-Clément, Heide Schreiber-Facklam(Klinikum Konstanz), Gad Singer(Kantonsspital Baden), Coya Tapia(University Hospital of Bern), Urs Wagner(Union Bank of Switzerland), Mauro G. Mastropasqua(University of Milan), Giuseppe Viale(University of Milan), Hans-Anton Lehr(University Hospital of Lausanne)
PLoS ONE
May 25, 2012
Cited by 226Open Access
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Abstract

UNLABELLED: Adjuvant chemotherapy decisions in breast cancer are increasingly based on the pathologist's assessment of tumor proliferation. The Swiss Working Group of Gyneco- and Breast Pathologists has surveyed inter- and intraobserver consistency of Ki-67-based proliferative fraction in breast carcinomas. METHODS: Five pathologists evaluated MIB-1-labeling index (LI) in ten breast carcinomas (G1, G2, G3) by counting and eyeballing. In the same way, 15 pathologists all over Switzerland then assessed MIB-1-LI on three G2 carcinomas, in self-selected or pre-defined areas of the tumors, comparing centrally immunostained slides with slides immunostained in the different laboratoires. To study intra-observer variability, the same tumors were re-examined 4 months later. RESULTS: The Kappa values for the first series of ten carcinomas of various degrees of differentiation showed good to very good agreement for MIB-1-LI (Kappa 0.56-0.72). However, we found very high inter-observer variabilities (Kappa 0.04-0.14) in the read-outs of the G2 carcinomas. It was not possible to explain the inconsistencies exclusively by any of the following factors: (i) pathologists' divergent definitions of what counts as a positive nucleus (ii) the mode of assessment (counting vs. eyeballing), (iii) immunostaining technique, and (iv) the selection of the tumor area in which to count. Despite intensive confrontation of all participating pathologists with the problem, inter-observer agreement did not improve when the same slides were re-examined 4 months later (Kappa 0.01-0.04) and intra-observer agreement was likewise poor (Kappa 0.00-0.35). CONCLUSION: Assessment of mid-range Ki-67-LI suffers from high inter- and intra-observer variability. Oncologists should be aware of this caveat when using Ki-67-LI as a basis for treatment decisions in moderately differentiated breast carcinomas.


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