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A Retrospective Evaluation of Chemotherapy Overdoses in Dogs and Cats
Chemotherapy overdoses (ODs) are severe complications that can occur following the use of antineoplastics. However, little is known about chemotherapy ODs in veterinary medicine. The goals of this retrospective study were to report the occurrence, type, and cause of known chemotherapy ODs in compani...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492923/ https://www.ncbi.nlm.nih.gov/pubmed/34631850 http://dx.doi.org/10.3389/fvets.2021.718967 |
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author | Musser, Margaret L. Curran, Kaitlin M. Flesner, Brian K. Johannes, Chad M. |
author_facet | Musser, Margaret L. Curran, Kaitlin M. Flesner, Brian K. Johannes, Chad M. |
author_sort | Musser, Margaret L. |
collection | PubMed |
description | Chemotherapy overdoses (ODs) are severe complications that can occur following the use of antineoplastics. However, little is known about chemotherapy ODs in veterinary medicine. The goals of this retrospective study were to report the occurrence, type, and cause of known chemotherapy ODs in companion animal medicine. The American College of Veterinary Internal Medicine oncology and internal medicine listservs were solicited for chemotherapy OD cases in dogs and cats. An OD was defined as administration of a chemotherapy dose 10% higher than intended, or at a shorter interval than planned. Twelve non-anthracycline ODs in 11 dogs, and 3 cat ODs, were collected. Overdoses in dogs included carboplatin, cyclophosphamide, L-asparaginase, lomustine, mustargen, vincristine, and vinorelbine. The cat ODs included doxorubicin and vincristine. In dogs, the median OD was 2.1x (range: 1.2–10x) the intended dose. All dogs survived the OD and developed a variety of gastrointestinal and hematologic toxicities of varying grades. Both cats with a 2.4x vincristine OD died despite supportive care. The cat who received a 2x OD of doxorubicin survived the event, experiencing Veterinary Cooperative Oncology Group–common terminology criteria for adverse events (VCOG) grade I thrombocytopenia and anemia, and VCOG grade II neutropenia. Chemotherapy ODs appear to be rare in veterinary medicine and are typically 2–3xs the intended dose. Clinical effects include VCOG grade I and II gastrointestinal distress and VCOG grade III and IV hematologic effects. With appropriate supportive care, most patients will survive the event. Life-threatening events are more common in cats following vincristine ODs. |
format | Online Article Text |
id | pubmed-8492923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84929232021-10-07 A Retrospective Evaluation of Chemotherapy Overdoses in Dogs and Cats Musser, Margaret L. Curran, Kaitlin M. Flesner, Brian K. Johannes, Chad M. Front Vet Sci Veterinary Science Chemotherapy overdoses (ODs) are severe complications that can occur following the use of antineoplastics. However, little is known about chemotherapy ODs in veterinary medicine. The goals of this retrospective study were to report the occurrence, type, and cause of known chemotherapy ODs in companion animal medicine. The American College of Veterinary Internal Medicine oncology and internal medicine listservs were solicited for chemotherapy OD cases in dogs and cats. An OD was defined as administration of a chemotherapy dose 10% higher than intended, or at a shorter interval than planned. Twelve non-anthracycline ODs in 11 dogs, and 3 cat ODs, were collected. Overdoses in dogs included carboplatin, cyclophosphamide, L-asparaginase, lomustine, mustargen, vincristine, and vinorelbine. The cat ODs included doxorubicin and vincristine. In dogs, the median OD was 2.1x (range: 1.2–10x) the intended dose. All dogs survived the OD and developed a variety of gastrointestinal and hematologic toxicities of varying grades. Both cats with a 2.4x vincristine OD died despite supportive care. The cat who received a 2x OD of doxorubicin survived the event, experiencing Veterinary Cooperative Oncology Group–common terminology criteria for adverse events (VCOG) grade I thrombocytopenia and anemia, and VCOG grade II neutropenia. Chemotherapy ODs appear to be rare in veterinary medicine and are typically 2–3xs the intended dose. Clinical effects include VCOG grade I and II gastrointestinal distress and VCOG grade III and IV hematologic effects. With appropriate supportive care, most patients will survive the event. Life-threatening events are more common in cats following vincristine ODs. Frontiers Media S.A. 2021-09-22 /pmc/articles/PMC8492923/ /pubmed/34631850 http://dx.doi.org/10.3389/fvets.2021.718967 Text en Copyright © 2021 Musser, Curran, Flesner and Johannes. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Veterinary Science Musser, Margaret L. Curran, Kaitlin M. Flesner, Brian K. Johannes, Chad M. A Retrospective Evaluation of Chemotherapy Overdoses in Dogs and Cats |
title | A Retrospective Evaluation of Chemotherapy Overdoses in Dogs and Cats |
title_full | A Retrospective Evaluation of Chemotherapy Overdoses in Dogs and Cats |
title_fullStr | A Retrospective Evaluation of Chemotherapy Overdoses in Dogs and Cats |
title_full_unstemmed | A Retrospective Evaluation of Chemotherapy Overdoses in Dogs and Cats |
title_short | A Retrospective Evaluation of Chemotherapy Overdoses in Dogs and Cats |
title_sort | retrospective evaluation of chemotherapy overdoses in dogs and cats |
topic | Veterinary Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492923/ https://www.ncbi.nlm.nih.gov/pubmed/34631850 http://dx.doi.org/10.3389/fvets.2021.718967 |
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