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  5. Limited Clinical Efficacy with Potential Adverse Events in a Pilot Study of Autologous Adoptive Cell Therapy in Canine Oral Malignant Melanoma
 
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Limited Clinical Efficacy with Potential Adverse Events in a Pilot Study of Autologous Adoptive Cell Therapy in Canine Oral Malignant Melanoma

Journal
Veterinary Sciences
Journal Volume
11
Journal Issue
4
ISSN
2306-7381
Date Issued
2024-03-28
Author(s)
Yuan-Yuan Xia
Kwan-Hwa Chi
TAI-CHING LIAO  
JIH-JONG LEE  
DOI
10.3390/vetsci11040150
URI
https://www.scopus.com/record/display.uri?eid=2-s2.0-85191702709&origin=resultslist
https://scholars.lib.ntu.edu.tw/handle/123456789/719614
Abstract
Adoptive cell therapy (ACT) has been studied in several human and canine cancers with some promising clinical outcomes but not in canine oral malignant melanoma (OMM). Our manuscript aimed to explore one kind of ACT, the ex vivo-expanded autologous immune cell infusion in canine OMM, as this tumor remains a treatment dilemma. The study recruited dogs with histopathological diagnoses of oral malignant melanoma, generated their peripheral blood mononuclear cells, expanded them into predominantly non-B non-T cells via stimulations of IL-15, IL-2, and IL-21, and then re-infused the cells into tumor-bearing dogs. Ten dogs were enrolled; three dogs did not report any adverse events; three had a mildly altered appetite; one had a mildly increased liver index, while the other three developed suspected anaphylaxis at different levels. The median progression-free interval was 49 days. Dogs with progressive disease during treatment had a shorter survival. This pilot study indicates limited efficacy with potential adverse events of this ACT. Most recruited patients were in a later stage and had macroscopic disease, which might affect the treatment efficacy. Further exploration of this cell therapy in an adjuvant setting, with adequate protocol modification and standardization, could still be considered.
Subjects
adoptive cell therapy
dog
immunotherapy
natural killer cell
oral malignant melanoma
SDGs

[SDGs]SDG3

Publisher
MDPI AG
Description
Article number: 150
Type
journal article

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