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Positron Emission Tomography-Computed Tomography Parameters Predict Efficacy of Immunotherapy in Head and Neck Squamous Cell Carcinomas

BACKGROUND: This study aims to assess the association between positron emission tomography-computed tomography (PET-CT) parameters and the response to immune checkpoint inhibitors in unresectable head and neck squamous cell carcinoma (HNSCC). METHODS: A total of 105 patients receiving immunotherapy...

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Autores principales: Zhang, Songtao, Zhang, Runfang, Gong, Wenbo, Wang, Chao, Zeng, Chen, Zhai, Yifei, Fang, Qigen, Dai, Liyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506113/
https://www.ncbi.nlm.nih.gov/pubmed/34650916
http://dx.doi.org/10.3389/fonc.2021.728040
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author Zhang, Songtao
Zhang, Runfang
Gong, Wenbo
Wang, Chao
Zeng, Chen
Zhai, Yifei
Fang, Qigen
Dai, Liyuan
author_facet Zhang, Songtao
Zhang, Runfang
Gong, Wenbo
Wang, Chao
Zeng, Chen
Zhai, Yifei
Fang, Qigen
Dai, Liyuan
author_sort Zhang, Songtao
collection PubMed
description BACKGROUND: This study aims to assess the association between positron emission tomography-computed tomography (PET-CT) parameters and the response to immune checkpoint inhibitors in unresectable head and neck squamous cell carcinoma (HNSCC). METHODS: A total of 105 patients receiving immunotherapy (pembrolizumab or sintilimab with/without cisplatin) were retrospectively enrolled in this study; pretreatment data regarding metabolic tumor volume (MTV) and maximum standardized uptake value (SUVmax) were collected. The primary interest of the study was objective response rate (ORR), and the secondary was progression−free survival (PFS). RESULTS: The mean total MTV was 40.6 cm(3) (range: 8.5–100.3), ORRs in tumors with total MTV of ≥40.6 and <40.6 cm(3) were 43.1% and 23.1%, respectively; the difference was statistically significant (p = 0.018). Survival analysis indicated similar PFS rates in the two groups (p = 0.057). The mean total SUVmax was 12.5, ORRs in tumors with total SUVmax ≥12.5 and <12.5 were 40.0% and 26.0%, respectively; the difference was not significant (p = 0.092). Survival analysis reported patients with total SUVmax of ≥12.5 had significantly worse PFS (p = 0.001) than patients with total SUVmax of <12.5. CONCLUSIONS: In HNSCC, total MTV ≥40.6 cm(3) translated into improved clinical response but not into better PFS; total SUVmax had no effect on clinical response, but total SUVmax ≥12.5 was associated with worse PFS.
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spelling pubmed-85061132021-10-13 Positron Emission Tomography-Computed Tomography Parameters Predict Efficacy of Immunotherapy in Head and Neck Squamous Cell Carcinomas Zhang, Songtao Zhang, Runfang Gong, Wenbo Wang, Chao Zeng, Chen Zhai, Yifei Fang, Qigen Dai, Liyuan Front Oncol Oncology BACKGROUND: This study aims to assess the association between positron emission tomography-computed tomography (PET-CT) parameters and the response to immune checkpoint inhibitors in unresectable head and neck squamous cell carcinoma (HNSCC). METHODS: A total of 105 patients receiving immunotherapy (pembrolizumab or sintilimab with/without cisplatin) were retrospectively enrolled in this study; pretreatment data regarding metabolic tumor volume (MTV) and maximum standardized uptake value (SUVmax) were collected. The primary interest of the study was objective response rate (ORR), and the secondary was progression−free survival (PFS). RESULTS: The mean total MTV was 40.6 cm(3) (range: 8.5–100.3), ORRs in tumors with total MTV of ≥40.6 and <40.6 cm(3) were 43.1% and 23.1%, respectively; the difference was statistically significant (p = 0.018). Survival analysis indicated similar PFS rates in the two groups (p = 0.057). The mean total SUVmax was 12.5, ORRs in tumors with total SUVmax ≥12.5 and <12.5 were 40.0% and 26.0%, respectively; the difference was not significant (p = 0.092). Survival analysis reported patients with total SUVmax of ≥12.5 had significantly worse PFS (p = 0.001) than patients with total SUVmax of <12.5. CONCLUSIONS: In HNSCC, total MTV ≥40.6 cm(3) translated into improved clinical response but not into better PFS; total SUVmax had no effect on clinical response, but total SUVmax ≥12.5 was associated with worse PFS. Frontiers Media S.A. 2021-09-28 /pmc/articles/PMC8506113/ /pubmed/34650916 http://dx.doi.org/10.3389/fonc.2021.728040 Text en Copyright © 2021 Zhang, Zhang, Gong, Wang, Zeng, Zhai, Fang and Dai https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Zhang, Songtao
Zhang, Runfang
Gong, Wenbo
Wang, Chao
Zeng, Chen
Zhai, Yifei
Fang, Qigen
Dai, Liyuan
Positron Emission Tomography-Computed Tomography Parameters Predict Efficacy of Immunotherapy in Head and Neck Squamous Cell Carcinomas
title Positron Emission Tomography-Computed Tomography Parameters Predict Efficacy of Immunotherapy in Head and Neck Squamous Cell Carcinomas
title_full Positron Emission Tomography-Computed Tomography Parameters Predict Efficacy of Immunotherapy in Head and Neck Squamous Cell Carcinomas
title_fullStr Positron Emission Tomography-Computed Tomography Parameters Predict Efficacy of Immunotherapy in Head and Neck Squamous Cell Carcinomas
title_full_unstemmed Positron Emission Tomography-Computed Tomography Parameters Predict Efficacy of Immunotherapy in Head and Neck Squamous Cell Carcinomas
title_short Positron Emission Tomography-Computed Tomography Parameters Predict Efficacy of Immunotherapy in Head and Neck Squamous Cell Carcinomas
title_sort positron emission tomography-computed tomography parameters predict efficacy of immunotherapy in head and neck squamous cell carcinomas
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506113/
https://www.ncbi.nlm.nih.gov/pubmed/34650916
http://dx.doi.org/10.3389/fonc.2021.728040
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