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(18)F-Fludeoxyglucose PET/CT in SCLC: Analysis of the CONVERT Randomized Controlled Trial

INTRODUCTION: We used phase-3 CONVERT trial data to investigate the impact of fludeoxyglucose F 18 ((18)F-FDG) positron emission tomography (PET)/computed tomography (CT) in SCLC. METHODS: CONVERT randomized patients with limited-stage SCLC to twice-daily (45 Gy in 30 fractions) or once-daily (66 Gy...

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Autores principales: Manoharan, Prakash, Salem, Ahmed, Mistry, Hitesh, Gornall, Michael, Harden, Susan, Julyan, Peter, Locke, Imogen, McAleese, Jonathan, McMenemin, Rhona, Mohammed, Nazia, Snee, Michael, Woods, Sarah, Westwood, Thomas, Faivre-Finn, Corinne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6616906/
https://www.ncbi.nlm.nih.gov/pubmed/31002954
http://dx.doi.org/10.1016/j.jtho.2019.03.023
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author Manoharan, Prakash
Salem, Ahmed
Mistry, Hitesh
Gornall, Michael
Harden, Susan
Julyan, Peter
Locke, Imogen
McAleese, Jonathan
McMenemin, Rhona
Mohammed, Nazia
Snee, Michael
Woods, Sarah
Westwood, Thomas
Faivre-Finn, Corinne
author_facet Manoharan, Prakash
Salem, Ahmed
Mistry, Hitesh
Gornall, Michael
Harden, Susan
Julyan, Peter
Locke, Imogen
McAleese, Jonathan
McMenemin, Rhona
Mohammed, Nazia
Snee, Michael
Woods, Sarah
Westwood, Thomas
Faivre-Finn, Corinne
author_sort Manoharan, Prakash
collection PubMed
description INTRODUCTION: We used phase-3 CONVERT trial data to investigate the impact of fludeoxyglucose F 18 ((18)F-FDG) positron emission tomography (PET)/computed tomography (CT) in SCLC. METHODS: CONVERT randomized patients with limited-stage SCLC to twice-daily (45 Gy in 30 fractions) or once-daily (66 Gy in 33 fractions) chemoradiotherapy. Patients were divided into two groups in this unplanned analysis: those staged with conventional imaging (contrast-enhanced thorax and abdomen CT and brain imaging with or without bone scintigraphy) and those staged with (18)F-FDG PET/CT in addition. RESULTS: Data on a total of 540 patients were analyzed. Compared with patients who underwent conventional imaging (n = 231), patients also staged with (18)F-FDG PET/CT (n = 309) had a smaller gross tumor volume (p = 0.003), were less likely to have an increased pretreatment serum lactate dehydrogenase level (p = 0.035), and received more chemotherapy (p = 0.026). There were no significant differences in overall (hazard ratio = 0.87, 95% confidence interval: 0.70–1.08, p = 0.192) and progression-free survival (hazard ratio = 0.87, 95% confidence interval: 0.71–1.07], p = 0.198) between patients staged with or without (18)F-FDG PET/CT. In the conventional imaging group, we found no survival difference between patients staged with or without bone scintigraphy. Although there were no differences in delivered radiotherapy dose, (18)F-FDG PET/CT–staged patients received lower normal tissue (lung, heart, and esophagus) radiation doses. Apart from a higher incidence of late esophagitis in patients staged with conventional imaging (for grade ≥1, 19% versus 11%; [p = 0.012]), the incidence of acute and late radiotherapy-related toxicities was not different between the two groups. CONCLUSION: In CONVERT, survival outcomes were not significantly different in patients staged with or without (18)F-FDG PET/CT. However, this analysis cannot support the use or omission of (18)F-FDG PET/CT owing to study limitations.
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spelling pubmed-66169062019-07-22 (18)F-Fludeoxyglucose PET/CT in SCLC: Analysis of the CONVERT Randomized Controlled Trial Manoharan, Prakash Salem, Ahmed Mistry, Hitesh Gornall, Michael Harden, Susan Julyan, Peter Locke, Imogen McAleese, Jonathan McMenemin, Rhona Mohammed, Nazia Snee, Michael Woods, Sarah Westwood, Thomas Faivre-Finn, Corinne J Thorac Oncol Article INTRODUCTION: We used phase-3 CONVERT trial data to investigate the impact of fludeoxyglucose F 18 ((18)F-FDG) positron emission tomography (PET)/computed tomography (CT) in SCLC. METHODS: CONVERT randomized patients with limited-stage SCLC to twice-daily (45 Gy in 30 fractions) or once-daily (66 Gy in 33 fractions) chemoradiotherapy. Patients were divided into two groups in this unplanned analysis: those staged with conventional imaging (contrast-enhanced thorax and abdomen CT and brain imaging with or without bone scintigraphy) and those staged with (18)F-FDG PET/CT in addition. RESULTS: Data on a total of 540 patients were analyzed. Compared with patients who underwent conventional imaging (n = 231), patients also staged with (18)F-FDG PET/CT (n = 309) had a smaller gross tumor volume (p = 0.003), were less likely to have an increased pretreatment serum lactate dehydrogenase level (p = 0.035), and received more chemotherapy (p = 0.026). There were no significant differences in overall (hazard ratio = 0.87, 95% confidence interval: 0.70–1.08, p = 0.192) and progression-free survival (hazard ratio = 0.87, 95% confidence interval: 0.71–1.07], p = 0.198) between patients staged with or without (18)F-FDG PET/CT. In the conventional imaging group, we found no survival difference between patients staged with or without bone scintigraphy. Although there were no differences in delivered radiotherapy dose, (18)F-FDG PET/CT–staged patients received lower normal tissue (lung, heart, and esophagus) radiation doses. Apart from a higher incidence of late esophagitis in patients staged with conventional imaging (for grade ≥1, 19% versus 11%; [p = 0.012]), the incidence of acute and late radiotherapy-related toxicities was not different between the two groups. CONCLUSION: In CONVERT, survival outcomes were not significantly different in patients staged with or without (18)F-FDG PET/CT. However, this analysis cannot support the use or omission of (18)F-FDG PET/CT owing to study limitations. Elsevier 2019-07 /pmc/articles/PMC6616906/ /pubmed/31002954 http://dx.doi.org/10.1016/j.jtho.2019.03.023 Text en © 2019 International Association for the Study of Lung Cancer. Elsevier Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Manoharan, Prakash
Salem, Ahmed
Mistry, Hitesh
Gornall, Michael
Harden, Susan
Julyan, Peter
Locke, Imogen
McAleese, Jonathan
McMenemin, Rhona
Mohammed, Nazia
Snee, Michael
Woods, Sarah
Westwood, Thomas
Faivre-Finn, Corinne
(18)F-Fludeoxyglucose PET/CT in SCLC: Analysis of the CONVERT Randomized Controlled Trial
title (18)F-Fludeoxyglucose PET/CT in SCLC: Analysis of the CONVERT Randomized Controlled Trial
title_full (18)F-Fludeoxyglucose PET/CT in SCLC: Analysis of the CONVERT Randomized Controlled Trial
title_fullStr (18)F-Fludeoxyglucose PET/CT in SCLC: Analysis of the CONVERT Randomized Controlled Trial
title_full_unstemmed (18)F-Fludeoxyglucose PET/CT in SCLC: Analysis of the CONVERT Randomized Controlled Trial
title_short (18)F-Fludeoxyglucose PET/CT in SCLC: Analysis of the CONVERT Randomized Controlled Trial
title_sort (18)f-fludeoxyglucose pet/ct in sclc: analysis of the convert randomized controlled trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6616906/
https://www.ncbi.nlm.nih.gov/pubmed/31002954
http://dx.doi.org/10.1016/j.jtho.2019.03.023
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