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Peer-reviewed veterinary case report

KIT and tryptase patterns predict survival in dog skin mast cell

By Kiupel, M et al.·Published in Veterinary pathology·2004·Department of Pathobiology and Diagnostic Investigation, United States·View original on PubMed

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Original publication title: The use of KIT and tryptase expression patterns as prognostic tools for canine cutaneous mast cell tumors.

Species:
dog

Plain-English summary

A study looked at 100 dogs with skin tumors called mast cell tumors (MCTs) to find better ways to predict how these tumors will behave after surgery. Researchers found that certain patterns of a protein called KIT in the tumors could indicate a higher chance of the tumor coming back and a shorter survival time for the dogs. While the study didn't find a strong link with another protein called tryptase, the findings suggest that looking at KIT patterns could help vets give more accurate prognoses for dogs with these tumors.

People also search for: dog mast cell tumor prognosis · canine skin tumor treatment · what to expect after dog surgery for tumor

Abstract

Cutaneous mast cell tumors (MCTs) are one of the most common tumors in dogs. Currently, prognostic and therapeutic determinations for MCTs are primarily based on the histologic grade of the tumor, but a vast majority of MCTs are of an intermediate grade, and the prognostic relevance is highly questioned. A more detailed prognostic evaluation, especially of grade 2 canine MCTs, is greatly needed. To evaluate the prognostic significance of KIT and tryptase expression patterns in canine cutaneous MCTs, we studied 100 cutaneous MCTs from 100 dogs that had been treated with surgery only. The total survival and disease-free survival time and the time to local or distant recurrence of MCTs were recorded for all dogs. Using immunohistochemistry, 98 of these MCTs were stained with anti-KIT and antitryptase antibodies. Three KIT- and three tryptase-staining patterns were identified. The KIT-staining patterns were identified as 1) membrane-associated staining, 2) focal to stippled cytoplasmic staining with decreased membrane-associated staining, and 3) diffuse cytoplasmic staining. The tryptase-staining patterns were identified as 1) diffuse cytoplasmic staining, 2) stippled cytoplasmic staining, and 3) little to no cytoplasmic staining. Based on univariate and multivariate survival analysis, increased cytoplasmic KIT staining was significantly associated with an increased rate of local recurrence and a decreased survival rate. The tryptase-staining patterns were not significantly associated with any survival parameter. On the basis of these results, we propose a new prognostic classification of canine cutaneous MCTs, according to their KIT-staining pattern, that can be used for the routine prognostic evaluation of canine cutaneous MCTs.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/15232137/