Comparison of 5 Ki-67 antibodies regarding reproducibility and capacity to predict prognosis in breast cancer: does the antibody matter?

Although several antibodies are available for immunohistochemical detection of Ki-67, even the most commonly used MIB-1 has not been validated yet. Our aim was to compare 5 commercially available antibodies for detection of Ki-67 in terms of agreement and their ability in predicting prognosis of bre...

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Published inHuman pathology Vol. 65; pp. 31 - 40
Main Authors Ács, Balázs, Kulka, Janina, Kovács, Kristóf Attila, Teleki, Ivett, Tőkés, Anna-Mária, Meczker, Ágnes, Győrffy, Balázs, Madaras, Lilla, Krenács, Tibor, Szász, Attila Marcell
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.07.2017
Elsevier Limited
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ISSN0046-8177
1532-8392
DOI10.1016/j.humpath.2017.01.011

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Abstract Although several antibodies are available for immunohistochemical detection of Ki-67, even the most commonly used MIB-1 has not been validated yet. Our aim was to compare 5 commercially available antibodies for detection of Ki-67 in terms of agreement and their ability in predicting prognosis of breast cancer. Tissue microarrays were constructed from 378 breast cancer patients' representative formalin-fixed, paraffin-embedded tumor blocks. Five antibodies were used to detect Ki-67 expression: MIB-1 using chromogenic detection and immunofluorescent-labeled MIB-1, SP-6, 30-9, poly, and B56. Semiquantitative assessment was performed by 2 pathologists independently on digitized slides. To compare the 5 antibodies, intraclass correlation and concordance correlation coefficient were used. All the antibodies but immunofluorescent-labeled MIB-1 (at 20% and 30% thresholds, P=.993 and P=.342, respectively) and B56 (at 30% threshold, P=.288) separated high- and low-risk patient groups. However, there were a significant difference (P values for all comparisons≤.005) and a moderate concordance (intraclass correlation, 0.645) between their Ki-67 labeling index scores. The highest concordance was found between MIB-1 and poly (concordance correlation coefficient=0.785) antibodies. None of the antibodies except Ki-67 labeling index as detected by poly (P=.031) at 20% threshold and lymph node status (P<.001) were significantly linked to disease-free survival in multivariate analysis. At 30% threshold, this was reduced to lymph node status (P<.001) alone. Our results showed that there are considerable differences between the different Ki-67 antibodies in their capacity to detect proliferating tumor cells and to separate low- and high-risk breast cancer patient groups. •SP6, 30-9, poly, B56, MIB-1, and immunofluorescent-labeled MIB-1 antibodies were compared.•Significant difference occurred between all Ki-67 LI assessments of the 5 antibodies.•Highest concordance/agreement was observed between MIB-1 and poly, and 30-9 and poly.•All investigated Ki-67 antibodies have prognostic potential except MIB-1–IF and B56.•Only poly antibody was an independent predictor of prognosis at 20% threshold.
AbstractList Although several antibodies are available for immunohistochemical detection of Ki-67, even the most commonly used MIB-1 has not been validated yet. Our aim was to compare 5 commercially available antibodies for detection of Ki-67 in terms of agreement and their ability in predicting prognosis of breast cancer. Tissue microarrays were constructed from 378 breast cancer patients' representative formalin-fixed, paraffin-embedded tumor blocks. Five antibodies were used to detect Ki-67 expression: MIB-1 using chromogenic detection and immunofluorescent-labeled MIB-1, SP-6, 30-9, poly, and B56. Semiquantitative assessment was performed by 2 pathologists independently on digitized slides. To compare the 5 antibodies, intraclass correlation and concordance correlation coefficient were used. All the antibodies but immunofluorescent-labeled MIB-1 (at 20% and 30% thresholds,P=.993 andP=.342, respectively) and B56 (at 30% threshold,P=.288) separated high- and low-risk patient groups. However, there were a significant difference (Pvalues for all comparisons<=.005) and a moderate concordance (intraclass correlation,0.645) between their Ki-67 labeling index scores. The highest concordance was found between MIB-1 and poly (concordance correlation coefficient=0.785) antibodies. None of the antibodies except Ki-67 labeling index as detected by poly (P=.031) at 20% threshold and lymph node status (P<.001) were significantly linked to disease-free survival in multivariate analysis. At 30% threshold, this was reduced to lymph node status (P<.001) alone. Our results showed that there are considerable differences between the different Ki-67 antibodies in their capacity to detect proliferating tumor cells and to separate low- and high-risk breast cancer patient groups.
Although several antibodies are available for immunohistochemical detection of Ki-67, even the most commonly used MIB-1 has not been validated yet. Our aim was to compare 5 commercially available antibodies for detection of Ki-67 in terms of agreement and their ability in predicting prognosis of breast cancer. Tissue microarrays were constructed from 378 breast cancer patients' representative formalin-fixed, paraffin-embedded tumor blocks. Five antibodies were used to detect Ki-67 expression: MIB-1 using chromogenic detection and immunofluorescent-labeled MIB-1, SP-6, 30-9, poly, and B56. Semiquantitative assessment was performed by 2 pathologists independently on digitized slides. To compare the 5 antibodies, intraclass correlation and concordance correlation coefficient were used. All the antibodies but immunofluorescent-labeled MIB-1 (at 20% and 30% thresholds, P=.993 and P=.342, respectively) and B56 (at 30% threshold, P=.288) separated high- and low-risk patient groups. However, there were a significant difference (P values for all comparisons≤.005) and a moderate concordance (intraclass correlation, 0.645) between their Ki-67 labeling index scores. The highest concordance was found between MIB-1 and poly (concordance correlation coefficient=0.785) antibodies. None of the antibodies except Ki-67 labeling index as detected by poly (P=.031) at 20% threshold and lymph node status (P<.001) were significantly linked to disease-free survival in multivariate analysis. At 30% threshold, this was reduced to lymph node status (P<.001) alone. Our results showed that there are considerable differences between the different Ki-67 antibodies in their capacity to detect proliferating tumor cells and to separate low- and high-risk breast cancer patient groups. •SP6, 30-9, poly, B56, MIB-1, and immunofluorescent-labeled MIB-1 antibodies were compared.•Significant difference occurred between all Ki-67 LI assessments of the 5 antibodies.•Highest concordance/agreement was observed between MIB-1 and poly, and 30-9 and poly.•All investigated Ki-67 antibodies have prognostic potential except MIB-1–IF and B56.•Only poly antibody was an independent predictor of prognosis at 20% threshold.
Although several antibodies are available for immunohistochemical detection of Ki-67, even the most commonly used MIB-1 has not been validated yet. Our aim was to compare 5 commercially available antibodies for detection of Ki-67 in terms of agreement and their ability in predicting prognosis of breast cancer. Tissue microarrays were constructed from 378 breast cancer patients' representative formalin-fixed, paraffin-embedded tumor blocks. Five antibodies were used to detect Ki-67 expression: MIB-1 using chromogenic detection and immunofluorescent-labeled MIB-1, SP-6, 30-9, poly, and B56. Semiquantitative assessment was performed by 2 pathologists independently on digitized slides. To compare the 5 antibodies, intraclass correlation and concordance correlation coefficient were used. All the antibodies but immunofluorescent-labeled MIB-1 (at 20% and 30% thresholds, P=.993 and P=.342, respectively) and B56 (at 30% threshold, P=.288) separated high- and low-risk patient groups. However, there were a significant difference (P values for all comparisons≤.005) and a moderate concordance (intraclass correlation, 0.645) between their Ki-67 labeling index scores. The highest concordance was found between MIB-1 and poly (concordance correlation coefficient=0.785) antibodies. None of the antibodies except Ki-67 labeling index as detected by poly (P=.031) at 20% threshold and lymph node status (P<.001) were significantly linked to disease-free survival in multivariate analysis. At 30% threshold, this was reduced to lymph node status (P<.001) alone. Our results showed that there are considerable differences between the different Ki-67 antibodies in their capacity to detect proliferating tumor cells and to separate low- and high-risk breast cancer patient groups.
Summary Although several antibodies are available for immunohistochemical detection of Ki-67, even the most commonly used MIB-1 has not been validated yet. Our aim was to compare 5 commercially available antibodies for detection of Ki-67 in terms of agreement and their ability in predicting prognosis of breast cancer. Tissue microarrays were constructed from 378 breast cancer patients' representative formalin-fixed, paraffin-embedded tumor blocks. Five antibodies were used to detect Ki-67 expression: MIB-1 using chromogenic detection and immunofluorescent-labeled MIB-1, SP-6, 30-9, poly, and B56. Semiquantitative assessment was performed by 2 pathologists independently on digitized slides. To compare the 5 antibodies, intraclass correlation and concordance correlation coefficient were used. All the antibodies but immunofluorescent-labeled MIB-1 (at 20% and 30% thresholds, P = .993 and P = .342, respectively) and B56 (at 30% threshold, P = .288) separated high- and low-risk patient groups. However, there were a significant difference ( P values for all comparisons ≤.005) and a moderate concordance (intraclass correlation, 0.645) between their Ki-67 labeling index scores. The highest concordance was found between MIB-1 and poly (concordance correlation coefficient = 0.785) antibodies. None of the antibodies except Ki-67 labeling index as detected by poly ( P = .031) at 20% threshold and lymph node status ( P < .001) were significantly linked to disease-free survival in multivariate analysis. At 30% threshold, this was reduced to lymph node status ( P < .001) alone. Our results showed that there are considerable differences between the different Ki-67 antibodies in their capacity to detect proliferating tumor cells and to separate low- and high-risk breast cancer patient groups.
Author Győrffy, Balázs
Madaras, Lilla
Teleki, Ivett
Meczker, Ágnes
Ács, Balázs
Kovács, Kristóf Attila
Kulka, Janina
Szász, Attila Marcell
Tőkés, Anna-Mária
Krenács, Tibor
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Keywords Ki-67 antibody
Breast cancer
Prognosis
Multivariate analysis
Concordance
Language English
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Snippet Although several antibodies are available for immunohistochemical detection of Ki-67, even the most commonly used MIB-1 has not been validated yet. Our aim was...
Summary Although several antibodies are available for immunohistochemical detection of Ki-67, even the most commonly used MIB-1 has not been validated yet. Our...
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SubjectTerms Adult
Aged
Aged, 80 and over
Antibodies - immunology
Antibody Specificity
Automation
Biopsy
Breast cancer
Breast Neoplasms - chemistry
Breast Neoplasms - immunology
Breast Neoplasms - pathology
Breast Neoplasms - therapy
Cancer therapies
Cell cycle
Cell Proliferation
Chemotherapy
Concordance
Disease-Free Survival
Female
Fluorescent Antibody Technique
Gene expression
Histopathology
Humans
Immunoglobulins
Immunohistochemistry - methods
Ki-67 antibody
Ki-67 Antigen - analysis
Ki-67 Antigen - immunology
Lymphatic Metastasis
Medical prognosis
Middle Aged
Multivariate Analysis
Observer Variation
Pathology
Patients
Predictive Value of Tests
Prognosis
Proteins
Reproducibility
Reproducibility of Results
Retrospective Studies
Risk Assessment
Risk Factors
Software
Studies
Time Factors
Title Comparison of 5 Ki-67 antibodies regarding reproducibility and capacity to predict prognosis in breast cancer: does the antibody matter?
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0046817717300321
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https://dx.doi.org/10.1016/j.humpath.2017.01.011
https://www.ncbi.nlm.nih.gov/pubmed/28188752
https://www.proquest.com/docview/1929755806
https://www.proquest.com/docview/1867540091
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