Evidence map›Paper›PMID 38767567›Full record

ArticleVeterinary medicine and science2024

Prognostic role of the updated Kiel classification in canine high-grade T-cell lymphomas.

Urszula Jankowska, Dariusz Jagielski, Michał Czopowicz, Rafał Sapierzyński

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Article in Veterinary medicine and science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Urszula JankowskaBiałobrzeska Veterinary Clinic, Warsaw, Poland.ORCID 0000-0002-9202-5322
Dariusz JagielskiBiałobrzeska Veterinary Clinic, Warsaw, Poland.ORCID 0000-0002-0617-201X
Michał CzopowiczDivision of Veterinary Epidemiology and Economics, Institute of Veterinary Medicine, Warsaw University of Life Sciences (SGGW), Warsaw, Poland.ORCID 0000-0002-4238-8360
Rafał SapierzyńskiDivision of Animal Pathology, Department of Pathology and Veterinary Diagnostics, Institute of Veterinary Medicine, Warsaw University of Life Sciences (SGGW), Warsaw, Poland.ORCID 0000-0003-2111-5117

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of this study was to determine and describe the prognostic role of the morphological subtype determined according to the updated Kiel classification in dogs with high-grade T-cell lymphomas (HGTCLs) depending on the treatment applied.

objectivesThe HGTCLs were classified into three subtypes according to the updated Kiel classification: pleomorphic mixed (PM), lymphoblastic lymphoma/acute lymphoblastic leukaemia and plasmacytoid (P). The treatment was divided into a palliative therapy (PlT) group and a chemotherapy (ChT) group.

methodsThe study was conducted between 2009 and 2017, and it enrolled 58 dogs in which cytomorphological and immunocytochemistry diagnoses were HGTCL.

resultsOverall survival (OS) was significantly longer in the ChT group (median OS-4 months, interquartile range [IQR] from 2 to 8 months) than in the PlT group (median OS-6 weeks, IQR from 1 week to 3 months). In the PlT group, PM subtype and glucocorticosteroids (GCSs) treatment proved significantly and independently linked to longer OS and approximately three-fold lower risk of death during the study period (adjusted hazard ratio [HR CLINICAL SIGNIFICANCE: The morphological subtype of HGTCL has some prognostic value in dogs treated palliatively (with PM subtype associated with longer OS than P subtype); however, this effect is no longer visible when a dog is treated with chemotherapy.

Indexed as

Dog DiseasesLymphoma, T-CellAnimalsAntineoplastic AgentsDogsFemaleMalePrognosisRetrospective StudiesAntineoplastic Agentscytopathologydogsfine‐needle biopsyhigh‐grade lymphomaKiel classificationlymphoma

Identifiers

PMID38767567
PMCPMC11104423

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.