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Peer-reviewed veterinary case report

Cat with multiple myeloma treated successfully with bortezomib

By H. Tani et al.·Published in BMC Veterinary Research·2022·View original on Semantic Scholar

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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 diagnosed with multiple myeloma, a type of cancer that can cause symptoms like loss of appetite, fatigue, and vomiting. After failing to improve on a different treatment, the cat was given bortezomib, a medication typically used for this cancer in humans. Over six treatment cycles, the cat's symptoms disappeared, and tests showed significant improvement, including a reduction in harmful proteins in the blood. The cat tolerated the lower dose of bortezomib well and showed no signs of relapse months later, suggesting this treatment could be effective for other cats with the same condition.

People also search for: cat multiple myeloma treatment · bortezomib for cats · cat vomiting and fatigue · feline cancer symptoms · cat cancer treatment options

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/m 2 for first week and 1.0 mg/m 2 for second week in the first cycle. A dose of 0.7 mg/m 2 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/m 2 , while no recognizable toxicity was observed at a dose of 0.7 mg/m 2 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/m 2 , but not at 1.0 mg/m 2 . Bortezomib appears to be a drug worthy of further study for the treatment of feline MM.

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Original publication on Semantic Scholar: https://www.semanticscholar.org/paper/36324112