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Retrospective evaluation of nimustine use in the treatment of feline lymphoma

BACKGROUND: Nimustine, similar to lomustine, is an alkylating agent from the nitrosourea family. There have been some reports regarding lomustine treatment for tumour‐bearing cats. However, information regarding nimustine treatment for tumour‐bearing cats is limited. OBJECTIVES: To retrospectively e...

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Autores principales: Sakai, Kosei, Hatoya, Shingo, Furuya, Masaru, Nabetani, Tomoyo, Kanegi, Ryoji, Shimamura, Shunsuke, Tani, Hiroyuki, Shimada, Terumasa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8788965/
https://www.ncbi.nlm.nih.gov/pubmed/34599792
http://dx.doi.org/10.1002/vms3.652
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author Sakai, Kosei
Hatoya, Shingo
Furuya, Masaru
Nabetani, Tomoyo
Kanegi, Ryoji
Shimamura, Shunsuke
Tani, Hiroyuki
Shimada, Terumasa
author_facet Sakai, Kosei
Hatoya, Shingo
Furuya, Masaru
Nabetani, Tomoyo
Kanegi, Ryoji
Shimamura, Shunsuke
Tani, Hiroyuki
Shimada, Terumasa
author_sort Sakai, Kosei
collection PubMed
description BACKGROUND: Nimustine, similar to lomustine, is an alkylating agent from the nitrosourea family. There have been some reports regarding lomustine treatment for tumour‐bearing cats. However, information regarding nimustine treatment for tumour‐bearing cats is limited. OBJECTIVES: To retrospectively evaluate adverse events and clinical outcomes in tumour‐bearing cats receiving nimustine. METHODS: Information regarding diagnosis, treatment condition, adverse events, and clinical outcomes was collected in tumour‐bearing cats receiving nimustine through reviews of medical records. RESULTS: Nine cats with lymphoma were treated with nimustine in the primary therapy (n = 2) and in the rescue therapy (n = 7). Median starting dose of nimustine was 25 mg/m(2) (range: 20–30 mg/m(2)) with dosing interval of three weeks and 1–11 administrations. Adverse events were mild gastrointestinal toxicity (grade 1) including diarrhoea (n = 2) and vomiting (n = 2) and mild myelosuppression (grade 1 or 2) including thrombocytopenia (n = 3) and neutropenia (n = 1). No severe adverse events were observed. Progression‐free survival durations among cats receiving nimustine in the primary therapy and in the rescue therapy were 274–688 days (median: 481 days) and 9–671 days (median: 102 days), respectively. Overall survival durations among cats receiving nimustine in the primary therapy and in the rescue therapy were 275–745 days (median: 510 days) and 14–671 days (median: 109 days), respectively. CONCLUSIONS: Nimustine was well tolerated and showed clinical outcomes similar to lomustine in cats with lymphoma. These findings suggest that nimustine might be an alternative to lomustine in the treatment of feline lymphoma.
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spelling pubmed-87889652022-02-01 Retrospective evaluation of nimustine use in the treatment of feline lymphoma Sakai, Kosei Hatoya, Shingo Furuya, Masaru Nabetani, Tomoyo Kanegi, Ryoji Shimamura, Shunsuke Tani, Hiroyuki Shimada, Terumasa Vet Med Sci CATS BACKGROUND: Nimustine, similar to lomustine, is an alkylating agent from the nitrosourea family. There have been some reports regarding lomustine treatment for tumour‐bearing cats. However, information regarding nimustine treatment for tumour‐bearing cats is limited. OBJECTIVES: To retrospectively evaluate adverse events and clinical outcomes in tumour‐bearing cats receiving nimustine. METHODS: Information regarding diagnosis, treatment condition, adverse events, and clinical outcomes was collected in tumour‐bearing cats receiving nimustine through reviews of medical records. RESULTS: Nine cats with lymphoma were treated with nimustine in the primary therapy (n = 2) and in the rescue therapy (n = 7). Median starting dose of nimustine was 25 mg/m(2) (range: 20–30 mg/m(2)) with dosing interval of three weeks and 1–11 administrations. Adverse events were mild gastrointestinal toxicity (grade 1) including diarrhoea (n = 2) and vomiting (n = 2) and mild myelosuppression (grade 1 or 2) including thrombocytopenia (n = 3) and neutropenia (n = 1). No severe adverse events were observed. Progression‐free survival durations among cats receiving nimustine in the primary therapy and in the rescue therapy were 274–688 days (median: 481 days) and 9–671 days (median: 102 days), respectively. Overall survival durations among cats receiving nimustine in the primary therapy and in the rescue therapy were 275–745 days (median: 510 days) and 14–671 days (median: 109 days), respectively. CONCLUSIONS: Nimustine was well tolerated and showed clinical outcomes similar to lomustine in cats with lymphoma. These findings suggest that nimustine might be an alternative to lomustine in the treatment of feline lymphoma. John Wiley and Sons Inc. 2021-10-02 /pmc/articles/PMC8788965/ /pubmed/34599792 http://dx.doi.org/10.1002/vms3.652 Text en © 2021 The Authors. Veterinary Medicine and Science published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle CATS
Sakai, Kosei
Hatoya, Shingo
Furuya, Masaru
Nabetani, Tomoyo
Kanegi, Ryoji
Shimamura, Shunsuke
Tani, Hiroyuki
Shimada, Terumasa
Retrospective evaluation of nimustine use in the treatment of feline lymphoma
title Retrospective evaluation of nimustine use in the treatment of feline lymphoma
title_full Retrospective evaluation of nimustine use in the treatment of feline lymphoma
title_fullStr Retrospective evaluation of nimustine use in the treatment of feline lymphoma
title_full_unstemmed Retrospective evaluation of nimustine use in the treatment of feline lymphoma
title_short Retrospective evaluation of nimustine use in the treatment of feline lymphoma
title_sort retrospective evaluation of nimustine use in the treatment of feline lymphoma
topic CATS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8788965/
https://www.ncbi.nlm.nih.gov/pubmed/34599792
http://dx.doi.org/10.1002/vms3.652
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