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Outcome and toxicity assessment of feline small cell lymphoma: 56 cases (2000–2010)
Feline small cell lymphoma is associated with greater response to treatment and survival when compared to large cell lymphoma. Treatment‐associated toxicity, response to rescue chemotherapy and prognostic factors are largely unknown. This retrospective study was performed to identify treatment‐assoc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645816/ https://www.ncbi.nlm.nih.gov/pubmed/29067174 http://dx.doi.org/10.1002/vms3.9 |
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author | Pope, Kendra V. Tun, Alex E. McNeill, Conor J. Brown, Dorothy C. Krick, Erika L. |
author_facet | Pope, Kendra V. Tun, Alex E. McNeill, Conor J. Brown, Dorothy C. Krick, Erika L. |
author_sort | Pope, Kendra V. |
collection | PubMed |
description | Feline small cell lymphoma is associated with greater response to treatment and survival when compared to large cell lymphoma. Treatment‐associated toxicity, response to rescue chemotherapy and prognostic factors are largely unknown. This retrospective study was performed to identify treatment‐associated toxicity, response to rescue chemotherapy and treatment outcome for cats diagnosed with small cell lymphoma of various anatomic locations. Medical records from 56 cats were evaluated. All cats were treated with glucocorticoid and chlorambucil with discontinuation of treatment recommended at 1 year if complete clinical response was documented. Chemotherapy toxicity was uncommon (33.9%) and generally mild. Grade III or IV hepatotoxicity was documented in 10.7% of patients. Overall response rate was 85.7% with glucocorticoid and chlorambucil. Median progression‐free survival was 1078 days. Overall response rate for rescue chemotherapy was 59%. Reintroduction of prednisone and chlorambucil was associated with significantly longer survival than prednisone and lomustine (>1500 vs. 492 days, P = 0.01). Median overall survival times for cats with lymphoma of the gastrointestinal tract was not significantly different from those with extra‐intestinal disease locations (1148 vs. 1375 days, P = 0.23). Median overall survival was 1317 days. Toxicity, other than hepatotoxicity was mild. Rescue chemotherapy with re‐introduction of glucocorticoids and chlorambucil was most successful. Discontinuation of glucocorticoid and chlorambucil with subsequent reintroduction as rescue chemotherapy appears to be just as effective as continued administration in cats. |
format | Online Article Text |
id | pubmed-5645816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56458162017-10-24 Outcome and toxicity assessment of feline small cell lymphoma: 56 cases (2000–2010) Pope, Kendra V. Tun, Alex E. McNeill, Conor J. Brown, Dorothy C. Krick, Erika L. Vet Med Sci Original Articles Feline small cell lymphoma is associated with greater response to treatment and survival when compared to large cell lymphoma. Treatment‐associated toxicity, response to rescue chemotherapy and prognostic factors are largely unknown. This retrospective study was performed to identify treatment‐associated toxicity, response to rescue chemotherapy and treatment outcome for cats diagnosed with small cell lymphoma of various anatomic locations. Medical records from 56 cats were evaluated. All cats were treated with glucocorticoid and chlorambucil with discontinuation of treatment recommended at 1 year if complete clinical response was documented. Chemotherapy toxicity was uncommon (33.9%) and generally mild. Grade III or IV hepatotoxicity was documented in 10.7% of patients. Overall response rate was 85.7% with glucocorticoid and chlorambucil. Median progression‐free survival was 1078 days. Overall response rate for rescue chemotherapy was 59%. Reintroduction of prednisone and chlorambucil was associated with significantly longer survival than prednisone and lomustine (>1500 vs. 492 days, P = 0.01). Median overall survival times for cats with lymphoma of the gastrointestinal tract was not significantly different from those with extra‐intestinal disease locations (1148 vs. 1375 days, P = 0.23). Median overall survival was 1317 days. Toxicity, other than hepatotoxicity was mild. Rescue chemotherapy with re‐introduction of glucocorticoids and chlorambucil was most successful. Discontinuation of glucocorticoid and chlorambucil with subsequent reintroduction as rescue chemotherapy appears to be just as effective as continued administration in cats. John Wiley and Sons Inc. 2015-10-29 /pmc/articles/PMC5645816/ /pubmed/29067174 http://dx.doi.org/10.1002/vms3.9 Text en © 2015 The Authors. Veterinary Medicine and Science Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Pope, Kendra V. Tun, Alex E. McNeill, Conor J. Brown, Dorothy C. Krick, Erika L. Outcome and toxicity assessment of feline small cell lymphoma: 56 cases (2000–2010) |
title | Outcome and toxicity assessment of feline small cell lymphoma: 56 cases (2000–2010) |
title_full | Outcome and toxicity assessment of feline small cell lymphoma: 56 cases (2000–2010) |
title_fullStr | Outcome and toxicity assessment of feline small cell lymphoma: 56 cases (2000–2010) |
title_full_unstemmed | Outcome and toxicity assessment of feline small cell lymphoma: 56 cases (2000–2010) |
title_short | Outcome and toxicity assessment of feline small cell lymphoma: 56 cases (2000–2010) |
title_sort | outcome and toxicity assessment of feline small cell lymphoma: 56 cases (2000–2010) |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645816/ https://www.ncbi.nlm.nih.gov/pubmed/29067174 http://dx.doi.org/10.1002/vms3.9 |
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