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Role of (18)FDG PET/CT metabolic parameters in predicting hematological toxicity during chemoradiotherapy for locally advanced cervical cancer

PURPOSE: The aim of this study is to evaluate the value of (18)FDG PET/CT metabolic parameters in predicting hematological toxicity (HT) during chemoradiotherapy (CRT) for locally advanced cervical cancer (LACC). METHODS AND MATERIALS: Forty-one patients with LACC undergoing concurrent CRT were retr...

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Autores principales: Meng, Tianyu, Meng, Xiangxi, Xu, Xiaoxia, Li, Xiaofan, Yang, Zhi, Li, Nan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433863/
https://www.ncbi.nlm.nih.gov/pubmed/36059649
http://dx.doi.org/10.3389/fonc.2022.956652
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author Meng, Tianyu
Meng, Xiangxi
Xu, Xiaoxia
Li, Xiaofan
Yang, Zhi
Li, Nan
author_facet Meng, Tianyu
Meng, Xiangxi
Xu, Xiaoxia
Li, Xiaofan
Yang, Zhi
Li, Nan
author_sort Meng, Tianyu
collection PubMed
description PURPOSE: The aim of this study is to evaluate the value of (18)FDG PET/CT metabolic parameters in predicting hematological toxicity (HT) during chemoradiotherapy (CRT) for locally advanced cervical cancer (LACC). METHODS AND MATERIALS: Forty-one patients with LACC undergoing concurrent CRT were retrospectively analyzed. The correlations among age, body mass index, FIGO stage, differentiation, maximum diameter of primary lesion, parametrial invasion, lymph node metastasis, pelvic active bone marrow volume (BM(ACT)), BM(ACT) volume percentage (BM(ACT)%), maximum standardized uptake value (SUVmax), metabolic tumor volume (MTV), total lesion glycolysis (TLG), and HT were analyzed using hypothesis testing and logistic regression. A p-value< 0.05 was considered significant unless otherwise specified. RESULTS: Among the 41 patients, 19 had grade 3–4 HT and 22 had grade 0–2 HT. Only SUVmax (Z = −1.961, p = 0.050) and BM(ACT)% (χ2 = 7.769, p = 0.020) showed statistically significant difference in univariate analysis. In logistic regression, grade 3–4 HT was not associated with SUVmax. The probability of HT occurrence in<30% BM(ACT)% was 0.071 times less than in 30%–40% BM(ACT)% (p = 0.010, OR = 0.071, 95% CI = 0.010–0.532), and the probability of HT occurrence in >40% BM(ACT)% was 0.148 times less than in 30%–40% BM(ACT)% (p = 0.037, OR = 0.148, 95% CI = 0.025–0.892). CONCLUSION: Baseline (18)FDG PET/CT BM(ACT)% could help predict the severity of HT during CRT for LACC.
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spelling pubmed-94338632022-09-02 Role of (18)FDG PET/CT metabolic parameters in predicting hematological toxicity during chemoradiotherapy for locally advanced cervical cancer Meng, Tianyu Meng, Xiangxi Xu, Xiaoxia Li, Xiaofan Yang, Zhi Li, Nan Front Oncol Oncology PURPOSE: The aim of this study is to evaluate the value of (18)FDG PET/CT metabolic parameters in predicting hematological toxicity (HT) during chemoradiotherapy (CRT) for locally advanced cervical cancer (LACC). METHODS AND MATERIALS: Forty-one patients with LACC undergoing concurrent CRT were retrospectively analyzed. The correlations among age, body mass index, FIGO stage, differentiation, maximum diameter of primary lesion, parametrial invasion, lymph node metastasis, pelvic active bone marrow volume (BM(ACT)), BM(ACT) volume percentage (BM(ACT)%), maximum standardized uptake value (SUVmax), metabolic tumor volume (MTV), total lesion glycolysis (TLG), and HT were analyzed using hypothesis testing and logistic regression. A p-value< 0.05 was considered significant unless otherwise specified. RESULTS: Among the 41 patients, 19 had grade 3–4 HT and 22 had grade 0–2 HT. Only SUVmax (Z = −1.961, p = 0.050) and BM(ACT)% (χ2 = 7.769, p = 0.020) showed statistically significant difference in univariate analysis. In logistic regression, grade 3–4 HT was not associated with SUVmax. The probability of HT occurrence in<30% BM(ACT)% was 0.071 times less than in 30%–40% BM(ACT)% (p = 0.010, OR = 0.071, 95% CI = 0.010–0.532), and the probability of HT occurrence in >40% BM(ACT)% was 0.148 times less than in 30%–40% BM(ACT)% (p = 0.037, OR = 0.148, 95% CI = 0.025–0.892). CONCLUSION: Baseline (18)FDG PET/CT BM(ACT)% could help predict the severity of HT during CRT for LACC. Frontiers Media S.A. 2022-08-18 /pmc/articles/PMC9433863/ /pubmed/36059649 http://dx.doi.org/10.3389/fonc.2022.956652 Text en Copyright © 2022 Meng, Meng, Xu, Li, Yang and Li 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
Meng, Tianyu
Meng, Xiangxi
Xu, Xiaoxia
Li, Xiaofan
Yang, Zhi
Li, Nan
Role of (18)FDG PET/CT metabolic parameters in predicting hematological toxicity during chemoradiotherapy for locally advanced cervical cancer
title Role of (18)FDG PET/CT metabolic parameters in predicting hematological toxicity during chemoradiotherapy for locally advanced cervical cancer
title_full Role of (18)FDG PET/CT metabolic parameters in predicting hematological toxicity during chemoradiotherapy for locally advanced cervical cancer
title_fullStr Role of (18)FDG PET/CT metabolic parameters in predicting hematological toxicity during chemoradiotherapy for locally advanced cervical cancer
title_full_unstemmed Role of (18)FDG PET/CT metabolic parameters in predicting hematological toxicity during chemoradiotherapy for locally advanced cervical cancer
title_short Role of (18)FDG PET/CT metabolic parameters in predicting hematological toxicity during chemoradiotherapy for locally advanced cervical cancer
title_sort role of (18)fdg pet/ct metabolic parameters in predicting hematological toxicity during chemoradiotherapy for locally advanced cervical cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433863/
https://www.ncbi.nlm.nih.gov/pubmed/36059649
http://dx.doi.org/10.3389/fonc.2022.956652
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