Combination toceranib and lomustine shows frequent high grade toxicities when used for treatment of non-resectable or recurrent mast cell tumours in dogs: A European multicentre study

S. Bavcar, J. De Vos, M. Kessler, P. De Fornel, P. Buracco, S. Murphy, J. Hirschberger, David Argyle

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

Mast cell tumours (MCTs) in dogs can present in a variety of forms. Non-resectable, recurrent or metastatic MCTs usually carry a poor prognosis and present a therapeutic challenge. Both toceranib and lomustine have shown single agent activity against MCTs in dogs. In this study, 10 dogs with advanced MCTs were enrolled prospectively and treated with toceranib (median dose 2.7 mg/kg orally every other day), lomustine (median dose 60 mg/m2 orally every 3 weeks) and prednisolone (1 mg/kg orally every other day, alternating with toceranib). Severe adverse events (SAEs), requiring alterations in the protocol, occurred in all dogs. The objective response rate was 50%. Three dogs died or were euthanased due to SAEs and therefore enrolment of new dogs was discontinued prematurely. A long term response (> 1 year) was observed in two dogs. Modifications of the protocol are required for future prospective studies.
Original languageEnglish
Pages (from-to)1-6
JournalThe Veterinary Journal
Volume224
Early online date3 May 2017
DOIs
Publication statusPublished - Jun 2017

Keywords / Materials (for Non-textual outputs)

  • Canine
  • Mast cell tumour
  • Toceranib
  • Lomustine
  • Adverse events

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