Canine Mammary Tumors

Author:

Peña L.1,Gama A.2,Goldschmidt M. H.3,Abadie J.4,Benazzi C.5,Castagnaro M.6,Díez L.1,Gärtner F.7,Hellmén E.8,Kiupel M.9,Millán Y.10,Miller M. A.11,Nguyen F.4,Poli A.12,Sarli G.5,Zappulli V.6,Mulas J. Martín de las10

Affiliation:

1. Department Animal Medicine, Surgery and Pathology, Complutense University of Madrid, Madrid, Spain

2. Animal and Veterinary Research Centre (CECAV), University of Trás-os-Montes and Alto Douro (UTAD), Vila Real, Portugal

3. Laboratory of Pathology and Toxicology, University of Pennsylvania, School of Veterinary Medicine, Philadelphia, PA, USA

4. LUNAM University, Oniris, AMaROC Unit, Nantes, France

5. Department of Veterinary Medical Sciences, University of Bologna, Ozzano Emilia (BO), Italy

6. Department of Comparative Biomedicine and Food Science, University of Padua, Padua, Italy

7. Institute of Pathology and Molecular Immunology of the University of Porto (IPATIMUP) and Institute of Biomedical Science Abel Salazar, University of Porto  (ICBAS-UP), Porto, Portugal

8. Department of Anatomy, Physiology and Biochemistry, Swedish University of Agricultural Sciences, Uppsala, Sweden

9. Diagnostic Center for Population and Animal Health, Department of Pathobiology and Diagnostic Investigation, Michigan State University, East Lansing, MI, USA

10. Department of Comparative Pathology, University of Córdoba, Córdoba, Spain

11. Department of Comparative Pathobiology, Purdue University, West Lafayette, IN, USA

12. Department of Veterinary Sciences, University of Pisa, Pisa, Italy

Abstract

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.

Publisher

SAGE Publications

Subject

General Veterinary

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