Prognostic factors and outcome in cats with thymic epithelial tumours: 64 cases (1999‐2021)

Author:

Marks T. A.1,Rossanese M.1,Yale A. D.1,Stewart S.1,Smallwood K.2,Rigas K.3,Guillén A.1ORCID

Affiliation:

1. Royal Veterinary College Hatfield AL9 7TA UK

2. North Downs Specialist Referrals Bletchingley RH1 4QP UK

3. Southfields Veterinary Specialists Basildon Essex SS14 3AP UK

Abstract

ObjectivesTo describe the clinical presentation, treatment and outcomes of cats diagnosed with thymic epithelial tumours and to determine prognostic factors for survival and recurrence.Materials and MethodsClinical records of cats diagnosed with a thymic epithelial tumour between 1999 and 2021 at three referral institutions were retrospectively reviewed.ResultsSixty‐four cats were included. Paraneoplastic syndromes were present in nine cats and metastatic disease was seen in two cats, one at diagnosis and one at the time of recurrence. Median tumour diameter was 6 cm (range, 2 to 15) and a cystic appearance was described on imaging in 25 cats. Surgical excision was attempted in 54 cats with a perioperative mortality rate of 11%.Median survival time for cats surviving to hospital discharge was 897 days (range, 21 to 3322). The 1‐, 2‐ and 5‐year survival rates for surgically treated thymic epithelial tumour were 86%, 70% and 66%, respectively. Survival was longer for cats with Masaoka‐Koga stage I and II tumours compared to stages III and IV (1366 days versus 454 days; P=0.002). Masaoka‐Koga stage was the only significant prognostic factor detected on multi‐variable analysis, with stage III and IV tumours associated with increased risk of death (hazard ratio: 5.67, 95% confidence interval: 1.29 to 24.91, P=.021). Tumour recurrence occurred in 11 cats at a median of 564 days (range, 93 to 1095); no significant prognostic factors for recurrence were identified.Clinical SignificanceCats with thymic epithelial tumours had a good long‐term prognosis following surgery. Tumour recurrence can occur late in the disease course and ongoing monitoring should therefore be considered. Masaoka‐Koga stage may influence survival time and could be used to predict outcome.

Publisher

Wiley

Subject

Small Animals

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