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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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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. |
format | Online Article Text |
id | pubmed-6616906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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