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Lomustine, methotrexate and cytarabine chemotherapy as a rescue treatment for feline lymphoma
OBJECTIVES: The aim of this study was to assess the efficacy and tolerability of lomustine, methotrexate and cytarabine chemotherapy as rescue treatment for feline lymphoma. METHODS: The medical records of 13 cats treated with lomustine, methotrexate and cytarabine for relapsed high-grade feline lym...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311916/ https://www.ncbi.nlm.nih.gov/pubmed/33176543 http://dx.doi.org/10.1177/1098612X20972066 |
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author | Smallwood, Katherine Harper, Aaron Blackwood, Laura |
author_facet | Smallwood, Katherine Harper, Aaron Blackwood, Laura |
author_sort | Smallwood, Katherine |
collection | PubMed |
description | OBJECTIVES: The aim of this study was to assess the efficacy and tolerability of lomustine, methotrexate and cytarabine chemotherapy as rescue treatment for feline lymphoma. METHODS: The medical records of 13 cats treated with lomustine, methotrexate and cytarabine for relapsed high-grade feline lymphoma, at a single institution between 2013 and 2018, were examined. All anatomical types were included. Data were analysed using descriptive statistics. RESULTS: Nine cats received all three drugs and four cats received only two drugs owing to progressive disease. In cats that received (or in which there was intention to treat with) all three drugs, 6/13 (46%) demonstrated a complete or partial response to chemotherapy. Treatment was generally well tolerated, although two cats experienced Veterinary Comparative Oncology Group (VCOG) grade 3 neutropenia and one cat experienced VCOG grade 3 thrombocytopenia. The median progression-free survival was 61 days (range 16–721 days). CONCLUSIONS AND RELEVANCE: CHOP-(cyclophosphamide, doxorubicin, vincristine, prednisolone) and COP-based protocols are established first-line chemotherapy for feline lymphoma, but standard rescue protocols are lacking. Lomustine has become a popular single-agent option, but prolonged or cumulative myelosuppression can result in treatment delays, risking relapse. Therefore, a multidrug lomustine-based protocol may be advantageous, and, from first principles, should also better overcome resistance. This study suggests that lomustine, methotrexate and cytarabine may represent an efficacious and well-tolerated protocol for feline lymphoma rescue. |
format | Online Article Text |
id | pubmed-8311916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-83119162021-08-06 Lomustine, methotrexate and cytarabine chemotherapy as a rescue treatment for feline lymphoma Smallwood, Katherine Harper, Aaron Blackwood, Laura J Feline Med Surg Original Articles OBJECTIVES: The aim of this study was to assess the efficacy and tolerability of lomustine, methotrexate and cytarabine chemotherapy as rescue treatment for feline lymphoma. METHODS: The medical records of 13 cats treated with lomustine, methotrexate and cytarabine for relapsed high-grade feline lymphoma, at a single institution between 2013 and 2018, were examined. All anatomical types were included. Data were analysed using descriptive statistics. RESULTS: Nine cats received all three drugs and four cats received only two drugs owing to progressive disease. In cats that received (or in which there was intention to treat with) all three drugs, 6/13 (46%) demonstrated a complete or partial response to chemotherapy. Treatment was generally well tolerated, although two cats experienced Veterinary Comparative Oncology Group (VCOG) grade 3 neutropenia and one cat experienced VCOG grade 3 thrombocytopenia. The median progression-free survival was 61 days (range 16–721 days). CONCLUSIONS AND RELEVANCE: CHOP-(cyclophosphamide, doxorubicin, vincristine, prednisolone) and COP-based protocols are established first-line chemotherapy for feline lymphoma, but standard rescue protocols are lacking. Lomustine has become a popular single-agent option, but prolonged or cumulative myelosuppression can result in treatment delays, risking relapse. Therefore, a multidrug lomustine-based protocol may be advantageous, and, from first principles, should also better overcome resistance. This study suggests that lomustine, methotrexate and cytarabine may represent an efficacious and well-tolerated protocol for feline lymphoma rescue. SAGE Publications 2020-11-12 2021-08 /pmc/articles/PMC8311916/ /pubmed/33176543 http://dx.doi.org/10.1177/1098612X20972066 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Smallwood, Katherine Harper, Aaron Blackwood, Laura Lomustine, methotrexate and cytarabine chemotherapy as a rescue treatment for feline lymphoma |
title | Lomustine, methotrexate and cytarabine chemotherapy as a rescue treatment for feline lymphoma |
title_full | Lomustine, methotrexate and cytarabine chemotherapy as a rescue treatment for feline lymphoma |
title_fullStr | Lomustine, methotrexate and cytarabine chemotherapy as a rescue treatment for feline lymphoma |
title_full_unstemmed | Lomustine, methotrexate and cytarabine chemotherapy as a rescue treatment for feline lymphoma |
title_short | Lomustine, methotrexate and cytarabine chemotherapy as a rescue treatment for feline lymphoma |
title_sort | lomustine, methotrexate and cytarabine chemotherapy as a rescue treatment for feline lymphoma |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311916/ https://www.ncbi.nlm.nih.gov/pubmed/33176543 http://dx.doi.org/10.1177/1098612X20972066 |
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