Peer-reviewed veterinary case report
Single IV dose of combretastatin A4-phosphate cuts tumor blood flow
By Abma, E et al.·Published in Veterinary and comparative oncology·2018·Small Animal Department·View original on PubMed →
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Original publication title: A single dose of intravenous combretastatin A4-phosphate is reasonably well tolerated and significantly reduces tumour vascularization in canine spontaneous cancers.
- Species:
- dog
Plain-English summary
Eight dogs with spontaneous solid tumors were treated with a single intravenous dose of a drug called combretastatin A4-phosphate (CA4P), which is designed to cut off blood flow to tumors. Most dogs tolerated the treatment well, with only one experiencing temporary weakness in all four legs. After treatment, two dogs showed a noticeable reduction in tumor size, and tests indicated that the blood flow to the tumors decreased significantly. This study suggests that CA4P could be a promising option for treating various types of cancer in dogs, with minimal side effects reported.
People also search for: dog cancer treatment options · combretastatin A4-phosphate for dogs · reducing tumor size in dogs · side effects of cancer treatment in dogs
Abstract
Combretastatin A4-phosphate (CA4P) is an anti-tumour vascular targeting agent which selectively blocks tumour blood flow. Research on CA4P in rodent tumour models is extensive; however, knowledge of its effect on spontaneous cancer is scarce. This study was conducted in canine patients with spontaneous solid tumours. The goal was to assess the toxicity and efficacy of CA4P in various spontaneous tumour types. Eight dogs with spontaneous tumours were enrolled and treated with a single dose of 75 mg mintravenous CA4P. The dogs were screened and monitored before and after injection. Pre- and post-treatment tumour blood flow was analysed in vivo by power Doppler ultrasound (PDUS) and contrast-enhanced ultrasound (CEUS). Vessel destruction and tumour necrosis were evaluated by histopathology. Clinically relevant toxicity was limited to one case of temporary tetraparesis; other adverse events were mild. Significant cardiovascular changes were mostly confined to changes in heart rate and cTnI levels. Macroscopic tumour size reduction was evident in 2 dogs. Based on PDUS and CEUS, CA4P induced a significant decrease in vascular index and tumour blood flow. Post-treatment, histopathology revealed a significant increase of necrotic tumoural tissue and a significant reduction in microvessel density in tumoural tissue. Anti-vascular and necrotizing effects of CA4P were documented in a variety of canine spontaneous cancers with only minimal side effects. This is the first study reporting the administration of CA4P to canine cancer patients with in vivo and ex vivo assessment, and a first step toward implementing CA4P in combination therapies in veterinary oncology patients. The use of CA4P in canine patients was approved and registered by the Belgian Federal Agency for Medicines and Health Products (FAMHP) (approval number 0002588, registration number 6518 ID 2F12).
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/29797763/