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Peer-reviewed veterinary case report

Dog with rare skin cancer improved by increasing oclacitinib dose

By Jungmin Lym et al.·Published in Frontiers in Veterinary Science·2025·Laboratory of Veterinary Internal Medicine, College of Veterinary Medicine, Chungbuk National University, Cheongju, Chungbuk, Republic of Korea, CH·View original on DOAJ

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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 confirming a rare skin cancer called Sézary syndrome, the dog was treated with a medication called oclacitinib. Initially, the dog showed significant improvement, but the skin lesions worsened after a few weeks, leading to an increase in the medication dose. While the higher dose helped again, the dog experienced a relapse after about two months. Despite the ups and downs, the treatment extended the dog's life longer than what has been seen in other cases of this condition.

People also search for: dog skin cancer treatment · Sézary syndrome in dogs · 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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Original publication on DOAJ: https://doi.org/10.3389/fvets.2025.1645059