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Evaluation of prognostic markers for canine mast cell tumors treated with vinblastine and prednisone

BACKGROUND: Canine cutaneous mast cell tumor (MCT) is a common neoplastic disease associated with a variable biologic behavior. Surgery remains the primary treatment for canine MCT; however, radiation therapy (RT) and chemotherapy are commonly used to treat aggressive MCT. The goals of this study we...

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Autores principales: Webster, Joshua D, Yuzbasiyan-Gurkan, Vilma, Thamm, Douglas H, Hamilton, Elizabeth, Kiupel, Matti
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2529280/
https://www.ncbi.nlm.nih.gov/pubmed/18700956
http://dx.doi.org/10.1186/1746-6148-4-32
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author Webster, Joshua D
Yuzbasiyan-Gurkan, Vilma
Thamm, Douglas H
Hamilton, Elizabeth
Kiupel, Matti
author_facet Webster, Joshua D
Yuzbasiyan-Gurkan, Vilma
Thamm, Douglas H
Hamilton, Elizabeth
Kiupel, Matti
author_sort Webster, Joshua D
collection PubMed
description BACKGROUND: Canine cutaneous mast cell tumor (MCT) is a common neoplastic disease associated with a variable biologic behavior. Surgery remains the primary treatment for canine MCT; however, radiation therapy (RT) and chemotherapy are commonly used to treat aggressive MCT. The goals of this study were to evaluate the prognostic utility of histologic grade, c-KIT mutations, KIT staining patterns, and the proliferation markers Ki67 and AgNORs in dogs postoperatively treated with vinblastine and prednisone +/- RT, and to compare the outcome of dogs treated with post-operative chemotherapy +/- RT to that of a prognostically matched group treated with surgery alone. Associations between prognostic markers and survival were evaluated. Disease-free intervals (DFI) and overall survival times (OS) of dogs with similar pretreatment prognostic indices postoperatively treated with chemotherapy were compared to dogs treated with surgery alone. RESULTS: Histologic grade 3 MCTs, MCTs with c-KIT mutations, MCTs with increased cytoplasmic KIT, and MCTs with increased Ki67 and AgNOR values were associated with decreased DFI and OS. Dogs with histologic grade 3 MCT had significantly increased DFI and OS when treated with chemotherapy vs. surgery alone. Although not statistically significant due to small sample sizes, MCTs with c-KIT mutations had increased DFI and OS when treated with chemotherapy vs. surgery alone. CONCLUSION AND CLINICAL IMPORTANCE: This study confirms the prognostic value of histologic grade, c-KIT mutations, KIT staining patterns, and proliferation analyses for canine MCT. Additionally, the results of this study further define the benefit of postoperative vinblastine and prednisone for histologic grade 3 MCTs.
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spelling pubmed-25292802008-09-05 Evaluation of prognostic markers for canine mast cell tumors treated with vinblastine and prednisone Webster, Joshua D Yuzbasiyan-Gurkan, Vilma Thamm, Douglas H Hamilton, Elizabeth Kiupel, Matti BMC Vet Res Research Article BACKGROUND: Canine cutaneous mast cell tumor (MCT) is a common neoplastic disease associated with a variable biologic behavior. Surgery remains the primary treatment for canine MCT; however, radiation therapy (RT) and chemotherapy are commonly used to treat aggressive MCT. The goals of this study were to evaluate the prognostic utility of histologic grade, c-KIT mutations, KIT staining patterns, and the proliferation markers Ki67 and AgNORs in dogs postoperatively treated with vinblastine and prednisone +/- RT, and to compare the outcome of dogs treated with post-operative chemotherapy +/- RT to that of a prognostically matched group treated with surgery alone. Associations between prognostic markers and survival were evaluated. Disease-free intervals (DFI) and overall survival times (OS) of dogs with similar pretreatment prognostic indices postoperatively treated with chemotherapy were compared to dogs treated with surgery alone. RESULTS: Histologic grade 3 MCTs, MCTs with c-KIT mutations, MCTs with increased cytoplasmic KIT, and MCTs with increased Ki67 and AgNOR values were associated with decreased DFI and OS. Dogs with histologic grade 3 MCT had significantly increased DFI and OS when treated with chemotherapy vs. surgery alone. Although not statistically significant due to small sample sizes, MCTs with c-KIT mutations had increased DFI and OS when treated with chemotherapy vs. surgery alone. CONCLUSION AND CLINICAL IMPORTANCE: This study confirms the prognostic value of histologic grade, c-KIT mutations, KIT staining patterns, and proliferation analyses for canine MCT. Additionally, the results of this study further define the benefit of postoperative vinblastine and prednisone for histologic grade 3 MCTs. BioMed Central 2008-08-13 /pmc/articles/PMC2529280/ /pubmed/18700956 http://dx.doi.org/10.1186/1746-6148-4-32 Text en Copyright © 2008 Webster et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Webster, Joshua D
Yuzbasiyan-Gurkan, Vilma
Thamm, Douglas H
Hamilton, Elizabeth
Kiupel, Matti
Evaluation of prognostic markers for canine mast cell tumors treated with vinblastine and prednisone
title Evaluation of prognostic markers for canine mast cell tumors treated with vinblastine and prednisone
title_full Evaluation of prognostic markers for canine mast cell tumors treated with vinblastine and prednisone
title_fullStr Evaluation of prognostic markers for canine mast cell tumors treated with vinblastine and prednisone
title_full_unstemmed Evaluation of prognostic markers for canine mast cell tumors treated with vinblastine and prednisone
title_short Evaluation of prognostic markers for canine mast cell tumors treated with vinblastine and prednisone
title_sort evaluation of prognostic markers for canine mast cell tumors treated with vinblastine and prednisone
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2529280/
https://www.ncbi.nlm.nih.gov/pubmed/18700956
http://dx.doi.org/10.1186/1746-6148-4-32
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