Peer-reviewed veterinary case report
Cat with itchy skin tumors found resistant to toceranib treatment
By Tani, Hiroyuki et al.·Published in Veterinary medicine and science·2024·Department of Veterinary Medicine, Japan·View original on PubMed →
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Original publication title: A case report of feline mast cell tumour with intertumoral heterogeneity: Identification of secondary mutations c.998G>C and c.2383G>C in KIT after resistance to toceranib.
- Species:
- cat
Plain-English summary
A 12-year-old male domestic cat with multiple skin tumors called mast cell tumors (MCTs) was brought in after experiencing itching and raw, bleeding skin for two weeks. The cat initially received treatments with two different chemotherapy drugs, but they did not work. Eventually, a medication called toceranib was given, which successfully shrank the tumors at first. However, after two months, the tumors became resistant to the treatment, and further tests revealed new mutations in the tumor cells that contributed to this resistance. This case highlights the complexity of treating MCTs in cats and the need for ongoing research into better treatment options.
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Abstract
A 12-year-old male domestic cat with multiple subcutaneous mast cell tumours (MCTs) presented with a 2-week history of pruritus and raw/bleeding skin from self-trauma at Kagoshima University Veterinary Teaching Hospital. Polymerase chain reaction (PCR) and histopathological analyses revealed intertumoral heterogeneity among tumour locations based on the mutation status of KIT. In addition, the expression pattern of KIT was characterized. After failed treatment with vinblastine (2.0-2.2 mg/m, intravenous administration, two doses in total) or nimustine (25 mg/m, intravenous administration, two doses in total), toceranib (2.2-2.6 mg/kg, orally administered, every other day) was administered to treat recurrent MCTs harbouring the KIT exon eight internal tandem duplication mutation, achieving a complete response. However, toceranib resistance developed 2 months after treatment initiation. Subsequent PCR analysis was conducted to identify the mutational status of KIT in each MCT and to detect the presence of secondary mutations associated with the acquisition of toceranib resistance. Secondary KIT mutations (c.998G>C and c.2383G>C), which were not initially detected in tumour cells at diagnosis, were identified after the development of resistance to toceranib. This indicates that the tumour cells in feline MCTs in the same case have diverse characteristics. Our findings encourage further investigation into the development of therapeutic strategies for feline MCTs, particularly focusing on the heterogeneous nature of KIT/KIT and overcoming acquired resistance to toceranib.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/39177283/