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Local tumour response to neoadjuvant therapy with 2‐aminoethyl dihydrogen phosphate in dogs with soft tissue sarcoma

BACKGROUND: In cases of soft tissue sarcoma (STS), neoadjuvant therapy is indicated to downstage the tumour prior to surgery to achieve enhanced local tumour control. The antineoplastic phospholipid compound 2‐aminoethyl dihydrogen phosphate (2‐AEH2F) is an alkyl phosphate ester capable of inhibitin...

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Autores principales: de Castro, Patrícia Ferreira, Maria, Durvanei Augusto, de Campos Fonseca Pinto, Ana Carolina Brandão, Patricio, Geni Cristina Fonseca, Matera, Julia Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122438/
https://www.ncbi.nlm.nih.gov/pubmed/35191220
http://dx.doi.org/10.1002/vms3.757
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author de Castro, Patrícia Ferreira
Maria, Durvanei Augusto
de Campos Fonseca Pinto, Ana Carolina Brandão
Patricio, Geni Cristina Fonseca
Matera, Julia Maria
author_facet de Castro, Patrícia Ferreira
Maria, Durvanei Augusto
de Campos Fonseca Pinto, Ana Carolina Brandão
Patricio, Geni Cristina Fonseca
Matera, Julia Maria
author_sort de Castro, Patrícia Ferreira
collection PubMed
description BACKGROUND: In cases of soft tissue sarcoma (STS), neoadjuvant therapy is indicated to downstage the tumour prior to surgery to achieve enhanced local tumour control. The antineoplastic phospholipid compound 2‐aminoethyl dihydrogen phosphate (2‐AEH2F) is an alkyl phosphate ester capable of inhibiting cell proliferation and inducing cell death by modifying the asymmetry of phospholipids in the cytoplasmic membrane OBJECTIVES: This clinical study was designed to investigate local antitumoural effects of neoadjuvant therapy with 2‐AEH2F in dogs with naturally occurring STS MATERIAL AND METHODS: Dogs (n = 11) received four consecutive weekly intravenous injections of 2‐AEH2F (70 mg/kg) prior to tumour resection. Tomographic (CT) and thermal (TE) images were used to investigate changes in tumour size and local temperature in response to treatment RESULTS: Comparative analysis of CT images (n = 9/11) failed to reveal complete or partial remission according to selected assessment criteria (RECIST, WHO and volumetric). Comparative analysis of TE images (n = 10/11) revealed significantly (p = 0.01416) lower temperatures in tumoural areas relative to surrounding tissues over the course of treatment CONCLUSIONS: 2‐AEH2F had no cytoreductive effects when used at doses and intervals described in this study. However, significant drop in skin temperatures recorded in tumoural areas suggest induction of physiological changes.
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spelling pubmed-91224382022-05-21 Local tumour response to neoadjuvant therapy with 2‐aminoethyl dihydrogen phosphate in dogs with soft tissue sarcoma de Castro, Patrícia Ferreira Maria, Durvanei Augusto de Campos Fonseca Pinto, Ana Carolina Brandão Patricio, Geni Cristina Fonseca Matera, Julia Maria Vet Med Sci DOGS BACKGROUND: In cases of soft tissue sarcoma (STS), neoadjuvant therapy is indicated to downstage the tumour prior to surgery to achieve enhanced local tumour control. The antineoplastic phospholipid compound 2‐aminoethyl dihydrogen phosphate (2‐AEH2F) is an alkyl phosphate ester capable of inhibiting cell proliferation and inducing cell death by modifying the asymmetry of phospholipids in the cytoplasmic membrane OBJECTIVES: This clinical study was designed to investigate local antitumoural effects of neoadjuvant therapy with 2‐AEH2F in dogs with naturally occurring STS MATERIAL AND METHODS: Dogs (n = 11) received four consecutive weekly intravenous injections of 2‐AEH2F (70 mg/kg) prior to tumour resection. Tomographic (CT) and thermal (TE) images were used to investigate changes in tumour size and local temperature in response to treatment RESULTS: Comparative analysis of CT images (n = 9/11) failed to reveal complete or partial remission according to selected assessment criteria (RECIST, WHO and volumetric). Comparative analysis of TE images (n = 10/11) revealed significantly (p = 0.01416) lower temperatures in tumoural areas relative to surrounding tissues over the course of treatment CONCLUSIONS: 2‐AEH2F had no cytoreductive effects when used at doses and intervals described in this study. However, significant drop in skin temperatures recorded in tumoural areas suggest induction of physiological changes. John Wiley and Sons Inc. 2022-02-22 /pmc/articles/PMC9122438/ /pubmed/35191220 http://dx.doi.org/10.1002/vms3.757 Text en © 2022 The Authors. Veterinary Medicine and Science published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle DOGS
de Castro, Patrícia Ferreira
Maria, Durvanei Augusto
de Campos Fonseca Pinto, Ana Carolina Brandão
Patricio, Geni Cristina Fonseca
Matera, Julia Maria
Local tumour response to neoadjuvant therapy with 2‐aminoethyl dihydrogen phosphate in dogs with soft tissue sarcoma
title Local tumour response to neoadjuvant therapy with 2‐aminoethyl dihydrogen phosphate in dogs with soft tissue sarcoma
title_full Local tumour response to neoadjuvant therapy with 2‐aminoethyl dihydrogen phosphate in dogs with soft tissue sarcoma
title_fullStr Local tumour response to neoadjuvant therapy with 2‐aminoethyl dihydrogen phosphate in dogs with soft tissue sarcoma
title_full_unstemmed Local tumour response to neoadjuvant therapy with 2‐aminoethyl dihydrogen phosphate in dogs with soft tissue sarcoma
title_short Local tumour response to neoadjuvant therapy with 2‐aminoethyl dihydrogen phosphate in dogs with soft tissue sarcoma
title_sort local tumour response to neoadjuvant therapy with 2‐aminoethyl dihydrogen phosphate in dogs with soft tissue sarcoma
topic DOGS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122438/
https://www.ncbi.nlm.nih.gov/pubmed/35191220
http://dx.doi.org/10.1002/vms3.757
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