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. 2017 Feb;19(2):185-193.
doi: 10.1177/1098612X15622237. Epub 2016 Jul 9.

Retrospective evaluation of toceranib phosphate (Palladia) in cats with oral squamous cell carcinoma

Affiliations

Retrospective evaluation of toceranib phosphate (Palladia) in cats with oral squamous cell carcinoma

Valerie Wiles et al. J Feline Med Surg. 2017 Feb.

Abstract

Objectives The aim of the study was to determine the clinical benefit and adverse event profile of toceranib phosphate in the treatment of feline oral squamous cell carcinoma (FOSCC). Methods Data obtained from the medical records of cats with oral squamous cell carcinoma diagnosed between 2010 and 2014 treated with toceranib phosphate were compared with medical record data from cats that did not receive toceranib, cytotoxic chemotherapy or radiation, to determine the response to toceranib treatment and adverse event profile of toceranib in cats. Concurrent use of non-steroidal anti-inflammatory drugs (NSAIDs) was allowed. Results Forty-six cats with FOSCC were included; 23 received treatment with toceranib (group 1) and 23 did not (group 2). The overall biological response rate in group 1 was 56.5%. Median survival time of toceranib-treated cats was significantly longer at 123 days compared with 45 days in cats not treated with toceranib ( P = 0.01). Cats achieving stable disease or better on toceranib therapy had significantly longer progression-free survival ( P <0.0001) and median survival ( P = 0.0042) times than those with progressive disease on toceranib. Administration of NSAIDs was also associated with significantly improved survival time ( P = 0.0038) among all cats. Anorexia was common but may reflect the underlying disease in these patients. Toceranib was well tolerated in cats, with the most common side effect being mild gastrointestinal toxicity. Conclusions and relevance Toceranib was well tolerated in cats with oral squamous cell carcinoma and may lead to improved survival times, especially when combined with NSAIDs. NSAID administration was also associated with improved survival times, and the relative benefit of toceranib and NSAIDs is difficult to determine from this retrospective study. Despite improvement in survival times, long-term survival in this patient population remained poor. As toceranib was well tolerated and may improve survival time, prospective evaluation of toceranib alone is warranted to assess response as a single agent and as part of multimodal therapy in an effort to achieve a more durable response in FOSCC.

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Conflict of interest statement

The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Figures

Figure 1
Figure 1
Kaplan–Meier survival curves for cats with feline oral squamous cell carcinoma. Cats in group 1 were treated with toceranib while cats in group 2 did not receive toceranib. Group 1 had a statistically significant longer survival than group 2 (P = 0.01)
Figure 2
Figure 2
Kaplan–Meier progression-free survival (PFS) curves for group 1 divided by response to toceranib. Cats achieving stable disease or better had a statistically significant longer PFS compared with cats with progressive disease (PD) (P <0.0001)
Figure 3
Figure 3
Kaplan–Meier survival curves for group 1 divided by response to toceranib. Cats achieving stable disease or better had statistically significant longer survival compared with cats with progressive disease (PD) on toceranib therapy (P = 0.0042)
Figure 4
Figure 4
Kaplan–Meier survival curve for all cats divided by use of non-steroidal anti-inflammatory drugs (NSAIDs). Cats given NSAIDs had significantly longer overall survival compared with those not treated with NSAIDs (P = 0.0038)

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