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

被引:10
作者
Bavcar, S. [1 ]
de Vos, J. [2 ]
Kessler, M. [3 ]
de Fornel, P. [4 ]
Buracco, P. [5 ]
Murphy, S. [6 ]
Hirschberger, J. [7 ]
Argyle, D. J. [1 ]
机构
[1] Univ Edinburgh, Royal Dick Sch Vet Studies, Edinburgh EH25 9RE, Midlothian, Scotland
[2] Anim Hosp Zeeuws Vlaanderen, De Ottenhorst, Vet Oncol Referral Ctr, Terneuzen, Netherlands
[3] Tierklin Hofheim, Hofheim, Germany
[4] Ctr Micen Vet, Creteil, France
[5] Univ Turin, Dipartimento Sci Vet, Turin, Italy
[6] Anim Hlth Trust, Newmarket, Suffolk, England
[7] Ludwig Maximilians Univ Munchen, Clin Small Anim Med, Munich, Germany
关键词
Canine; Mast cell tumour; Toceranib; Lomustine; Adverse events; TYROSINE KINASE INHIBITOR; VINBLASTINE CHEMOTHERAPY; PHASE-II; CCNU; PREDNISONE; EFFICACY; SU11654; HEPATOTOXICITY; NEOPLASMS; LYMPHOMA;
D O I
10.1016/j.tvjl.2017.04.010
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
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/m(2) 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. (C) 2017 Elsevier Ltd. All rights reserved.
引用
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页码:1 / 6
页数:6
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