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Peer-reviewed veterinary case report

Cat with multiple myeloma treated successfully with bortezomib

By Hiroyuki Tani et al.·Published in BMC Veterinary Research·2022·Department of Veterinary Clinical Pathology, Nippon Veterinary and Life Science University, GB·View original on DOAJ

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Original publication title: A feline case of multiple myeloma treated with bortezomib

Species:
cat

Plain-English summary

An 11-year-old male domestic cat was brought in for symptoms like not eating, being unusually tired, and vomiting. After initially failing treatment with melphalan and prednisolone for multiple myeloma (a type of cancer), the cat was started on bortezomib, a drug commonly used in humans for this condition. Over six treatment cycles, the cat's symptoms improved significantly, and tests showed that the cancer markers had disappeared. The cat tolerated the lower dose of bortezomib well, and as of the last follow-up, there were no signs of cancer returning.

People also search for: cat cancer treatment · bortezomib for cats · why is my cat vomiting and tired

Abstract

Abstract Background Multiple myeloma (MM) is an uncommon neoplasm in cats. There is no established standard of treatment due to the rare occurrence of this disease in cats. Bortezomib is a proteasome inhibitor that serves as the first-line drug for MM in humans, but its effectiveness currently is unknown in feline MM. We present here the case report of a feline MM that exhibited a favorable response to bortezomib. Case presentation The case was an 11-year-old non-castrated male domestic cat with light-chain MM presenting with clinical symptoms (anorexia, fatigue, and vomiting), mild azotemia, and pancytopenia. The cat failed on melphalan with prednisolone (MP), so bortezomib (Velcade) was initiated on Day 88. A total of 6 cycles of the treatment was performed, with each treatment cycle consisting of twice-weekly subcutaneous administration for 2 weeks followed by a 1-week rest. The dose of bortezomib was 0.7 mg/m2 for first week and 1.0 mg/m2 for second week in the first cycle. A dose of 0.7 mg/m2 was used for subsequent cycles. Prednisolone was used concomitantly in the first 2 cycles. Following treatment with bortezomib, clinical symptoms disappeared and a decrease in serum globulin and recovery of pancytopenia were noted. A monoclonal gammopathy, overproduction of serum immunoglobulin light chain, and Bence-Jones proteinuria that existed at diagnosis were undetectable on Day 123. A monoclonal gammopathy also was not detectable at the end of the bortezomib treatment (Day 213). Anorexia, fatigue, and marked bone marrow toxicity were experienced when bortezomib was administrated at a dose of 1.0 mg/m2, while no recognizable toxicity was observed at a dose of 0.7 mg/m2 throughout the treatment period. The case was placed on follow-up and there was no evidence of relapse as of Day 243. Conclusions Bortezomib was effective and durable for the treatment of this case of feline MM after failure with MP. Bortezomib was well-tolerated in this cat at a dose of 0.7 mg/m2, but not at 1.0 mg/m2. Bortezomib appears to be a drug worthy of further study for the treatment of feline MM.

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Original publication on DOAJ: https://doi.org/10.1186/s12917-022-03484-1