TY - JOUR
T1 - Canine Mammary Tumors
T2 - A Review and Consensus of Standard Guidelines on Epithelial and Myoepithelial Phenotype Markers, HER2, and Hormone Receptor Assessment Using Immunohistochemistry
AU - Pena, L.
AU - Gama, A.
AU - Goldschmidt, M. H.
AU - Abadie, J.
AU - Benazzi, C.
AU - Castagnaro, M.
AU - Diez, L.
AU - Gaertner, F.
AU - Hellmén, E.
AU - Kiupel, M.
AU - Millan, Y.
AU - Miller, M. A.
AU - Nguyen, F.
AU - Poli, A.
AU - Sarli, G.
AU - Zappulli, V.
AU - Martin de las Mulas, J.
PY - 2014
Y1 - 2014
N2 - Although there have been several studies on the use of immunohistochemical biomarkers of canine mammary tumors (CMTs), the results are difficult to compare. This article provides guidelines on the most useful immunohistochemical markers to standardize their use and understand how outcomes are measured, thus ensuring reproducibility of results. We have reviewed the biomarkers of canine mammary epithelial and myoepithelial cells and identified those biomarkers that are most useful and those biomarkers for invasion and lymph node micrometastatic disease. A 10% threshold for positive reaction for most of these markers is recommended. Guidelines on immunolabeling for HER2, estrogen receptors (ERs), and progesterone receptors (PRs) are provided along with the specific recommendations for interpretation of the results for each of these biomarkers in CMTs. Only 3+ HER2-positive tumors should be considered positive, as found in human breast cancer. The lack of any known response to adjuvant endocrine therapy of ER- and PR-positive CMTs prevents the use of the biological positive/negative threshold used in human breast cancer. Immunohistochemistry results of ER and PR in CMTs should be reported as the sum of the percentage of positive cells and the intensity of immunolabeling (Allred score). Incorporation of these recommendations in future studies, either prospective or retrospective, will provide a mechanism for the direct comparison of studies and will help to determine whether these biomarkers have prognostic significance. Finally, these biomarkers may ascertain the most appropriate treatment(s) for canine malignant mammary neoplasms.
AB - Although there have been several studies on the use of immunohistochemical biomarkers of canine mammary tumors (CMTs), the results are difficult to compare. This article provides guidelines on the most useful immunohistochemical markers to standardize their use and understand how outcomes are measured, thus ensuring reproducibility of results. We have reviewed the biomarkers of canine mammary epithelial and myoepithelial cells and identified those biomarkers that are most useful and those biomarkers for invasion and lymph node micrometastatic disease. A 10% threshold for positive reaction for most of these markers is recommended. Guidelines on immunolabeling for HER2, estrogen receptors (ERs), and progesterone receptors (PRs) are provided along with the specific recommendations for interpretation of the results for each of these biomarkers in CMTs. Only 3+ HER2-positive tumors should be considered positive, as found in human breast cancer. The lack of any known response to adjuvant endocrine therapy of ER- and PR-positive CMTs prevents the use of the biological positive/negative threshold used in human breast cancer. Immunohistochemistry results of ER and PR in CMTs should be reported as the sum of the percentage of positive cells and the intensity of immunolabeling (Allred score). Incorporation of these recommendations in future studies, either prospective or retrospective, will provide a mechanism for the direct comparison of studies and will help to determine whether these biomarkers have prognostic significance. Finally, these biomarkers may ascertain the most appropriate treatment(s) for canine malignant mammary neoplasms.
KW - canine mammary tumors
KW - immunohistochemistry
KW - phenotype markers
KW - HER2
KW - estrogen receptor
KW - progesterone receptor
KW - consensual recommendations
KW - canine mammary tumors
KW - immunohistochemistry
KW - phenotype markers
KW - HER2
KW - estrogen receptor
KW - progesterone receptor
KW - consensual recommendations
UR - https://res.slu.se/id/publ/52704
U2 - 10.1177/0300985813509388
DO - 10.1177/0300985813509388
M3 - Journal article
C2 - 24227007
SN - 0300-9858
VL - 51
SP - 127
EP - 145
JO - Veterinary Pathology
JF - Veterinary Pathology
IS - 1
ER -