Cargando…

Dose‐escalated simultaneously integrated boost radiation protocol fails to result in a survival advantage for sinonasal tumors in dogs

The prognosis for canine sinonasal tumors remains rather poor despite definitive‐intent radiotherapy (RT). Theoretical calculations predicted improved outcomes with simultaneously integrated boost (SIB) protocols. With the hypothesis of clinically detectable differences in outcome between groups, ou...

Descripción completa

Detalles Bibliográficos
Autores principales: Meier, Valeria, Staudinger, Chris, Körner, Maximilian, Soukup, Alena, Rohrer Bley, Carla
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/PMC9790663/
https://www.ncbi.nlm.nih.gov/pubmed/35347801
http://dx.doi.org/10.1111/vru.13086
_version_ 1784859229826318336
author Meier, Valeria
Staudinger, Chris
Körner, Maximilian
Soukup, Alena
Rohrer Bley, Carla
author_facet Meier, Valeria
Staudinger, Chris
Körner, Maximilian
Soukup, Alena
Rohrer Bley, Carla
author_sort Meier, Valeria
collection PubMed
description The prognosis for canine sinonasal tumors remains rather poor despite definitive‐intent radiotherapy (RT). Theoretical calculations predicted improved outcomes with simultaneously integrated boost (SIB) protocols. With the hypothesis of clinically detectable differences in outcome between groups, our retrospective study evaluated prognostic variables and outcome in dogs treated with regular versus SIB RT. Dogs with sinonasal tumors treated with either a regular (10 × 4.2 Gy) or new SIB protocol (10 × 4.83 Gy to macroscopic tumor) were included. Information regarding signalment, tumor stage, type, clinical signs, radiation toxicity, response, and outcome was collected. Forty‐nine dogs were included: 27 treated regularly and 22 treated with SIB RT. A total of 69.4% showed epistaxis, 6.1% showed epileptic seizures, 46.9% showed stage IV tumors, and 6.1% showed lymph node metastases. Early toxicity was mostly mild. Late grade 1 skin toxicity (alopecia/leucotrichia) was seen in 72.1% of dogs, and a possible grade 3 ocular toxicity (blindness) was seen in one dog. Complete/partial resolution of clinical signs was seen in 95.9% of patients as best clinical response and partial remission was seen as best imaging response in 34.7%. The median progression‐free survival (PFS) was 274 days (95% CI: 117–383) for regular and 300 days (95% CI: 143–451) for SIB RT, which was not significantly different (P = 0.42). Similarly, the median overall survival (OS) was 348 days (95% CI: 121–500) for regular and 381 days (95% CI: 295–634) for the SIB RT (P = 0.18). Stratified by protocol, the hazard ratio of stage IV versus stage I–III tumors was 2.29 (95% CI: 1.156‐4.551, P = 0.02) for OS but not PFS. All dogs showed acceptable toxicity. In contrast to theoretical predictions, however, we could not show a statistically significant better outcome with the new protocol.
format Online
Article
Text
id pubmed-9790663
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-97906632022-12-28 Dose‐escalated simultaneously integrated boost radiation protocol fails to result in a survival advantage for sinonasal tumors in dogs Meier, Valeria Staudinger, Chris Körner, Maximilian Soukup, Alena Rohrer Bley, Carla Vet Radiol Ultrasound Radiation Oncology The prognosis for canine sinonasal tumors remains rather poor despite definitive‐intent radiotherapy (RT). Theoretical calculations predicted improved outcomes with simultaneously integrated boost (SIB) protocols. With the hypothesis of clinically detectable differences in outcome between groups, our retrospective study evaluated prognostic variables and outcome in dogs treated with regular versus SIB RT. Dogs with sinonasal tumors treated with either a regular (10 × 4.2 Gy) or new SIB protocol (10 × 4.83 Gy to macroscopic tumor) were included. Information regarding signalment, tumor stage, type, clinical signs, radiation toxicity, response, and outcome was collected. Forty‐nine dogs were included: 27 treated regularly and 22 treated with SIB RT. A total of 69.4% showed epistaxis, 6.1% showed epileptic seizures, 46.9% showed stage IV tumors, and 6.1% showed lymph node metastases. Early toxicity was mostly mild. Late grade 1 skin toxicity (alopecia/leucotrichia) was seen in 72.1% of dogs, and a possible grade 3 ocular toxicity (blindness) was seen in one dog. Complete/partial resolution of clinical signs was seen in 95.9% of patients as best clinical response and partial remission was seen as best imaging response in 34.7%. The median progression‐free survival (PFS) was 274 days (95% CI: 117–383) for regular and 300 days (95% CI: 143–451) for SIB RT, which was not significantly different (P = 0.42). Similarly, the median overall survival (OS) was 348 days (95% CI: 121–500) for regular and 381 days (95% CI: 295–634) for the SIB RT (P = 0.18). Stratified by protocol, the hazard ratio of stage IV versus stage I–III tumors was 2.29 (95% CI: 1.156‐4.551, P = 0.02) for OS but not PFS. All dogs showed acceptable toxicity. In contrast to theoretical predictions, however, we could not show a statistically significant better outcome with the new protocol. John Wiley and Sons Inc. 2022-03-29 2022 /pmc/articles/PMC9790663/ /pubmed/35347801 http://dx.doi.org/10.1111/vru.13086 Text en © 2022 The Authors. Veterinary Radiology & Ultrasound published by Wiley Periodicals LLC on behalf of American College of Veterinary Radiology. 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 Radiation Oncology
Meier, Valeria
Staudinger, Chris
Körner, Maximilian
Soukup, Alena
Rohrer Bley, Carla
Dose‐escalated simultaneously integrated boost radiation protocol fails to result in a survival advantage for sinonasal tumors in dogs
title Dose‐escalated simultaneously integrated boost radiation protocol fails to result in a survival advantage for sinonasal tumors in dogs
title_full Dose‐escalated simultaneously integrated boost radiation protocol fails to result in a survival advantage for sinonasal tumors in dogs
title_fullStr Dose‐escalated simultaneously integrated boost radiation protocol fails to result in a survival advantage for sinonasal tumors in dogs
title_full_unstemmed Dose‐escalated simultaneously integrated boost radiation protocol fails to result in a survival advantage for sinonasal tumors in dogs
title_short Dose‐escalated simultaneously integrated boost radiation protocol fails to result in a survival advantage for sinonasal tumors in dogs
title_sort dose‐escalated simultaneously integrated boost radiation protocol fails to result in a survival advantage for sinonasal tumors in dogs
topic Radiation Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790663/
https://www.ncbi.nlm.nih.gov/pubmed/35347801
http://dx.doi.org/10.1111/vru.13086
work_keys_str_mv AT meiervaleria doseescalatedsimultaneouslyintegratedboostradiationprotocolfailstoresultinasurvivaladvantageforsinonasaltumorsindogs
AT staudingerchris doseescalatedsimultaneouslyintegratedboostradiationprotocolfailstoresultinasurvivaladvantageforsinonasaltumorsindogs
AT kornermaximilian doseescalatedsimultaneouslyintegratedboostradiationprotocolfailstoresultinasurvivaladvantageforsinonasaltumorsindogs
AT soukupalena doseescalatedsimultaneouslyintegratedboostradiationprotocolfailstoresultinasurvivaladvantageforsinonasaltumorsindogs
AT rohrerbleycarla doseescalatedsimultaneouslyintegratedboostradiationprotocolfailstoresultinasurvivaladvantageforsinonasaltumorsindogs