Peer-reviewed veterinary case report
Dog with rare skin cancer improved by higher oclacitinib dose
By Lym, Jungmin et al.·Published in Frontiers in veterinary science·2025·College of Veterinary Medicine, South Korea·View original on PubMed →
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Original publication title: Case Report: Dose-dependent response to oclacitinib in a dog with Sézary syndrome.
- Species:
- dog
Plain-English summary
A 10-year-old spayed female Yorkshire Terrier was brought in for multiple skin nodules, plaques, crusts, and severe itching. After tests confirmed she had a rare skin cancer called Sèzary syndrome, she was treated with a medication called oclacitinib. Initially, the lower dose helped her significantly, but her condition worsened after a few weeks, leading to an increase in the medication dose. While she showed improvement again, her symptoms returned after a couple of months. This case suggests that oclacitinib can provide temporary relief for dogs with Sèzary syndrome, but more research is needed on its long-term effectiveness.
People also search for: dog skin cancer treatment · Yorkshire Terrier itching · oclacitinib for dog skin problems
Abstract
Cutaneous epitheliotropic T-cell lymphoma (CETL) is a rare malignant canine skin tumor. Sézary syndrome, a rare and aggressive subtype of CETL, lacks established treatment guidelines in veterinary medicine. A 10-year-old, spayed female Yorkshire Terrier presented with multiple skin nodules, plaques, crusts, and pruritus. Histopathological and immunohistochemical evaluations confirmed CETL, and Sézary cells were identified in a peripheral blood smear, confirming Sézary syndrome. The dog was initially treated with oclacitinib 0.7 mg/kg twice daily. Marked clinical improvement was observed on day 15 with the disappearance of Sézary cells. However, by day 32, the skin lesions had worsened, and the oclacitinib dose was increased to 3 mg/kg twice daily. Subsequent improvements were noted within 12 days, although a relapse occurred on day 63. Immunohistochemical staining revealed moderate and diffuse cytoplasmic and nuclear expression of Janus kinase 1 (JAK1), an oclacitinib target. This case demonstrated that both low- and high-dose oclacitinib may offer temporary clinical benefits in dogs with Sézary syndrome, potentially via JAK1 inhibition. Although the duration of the response was limited, the survival period exceeded that of previously reported canine cases of Sézary syndrome. These findings support further investigation of Janus kinase inhibitors as therapeutic options for Sézary syndrome and other forms of CETL in veterinary patients.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/41473101/