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The optimal timing of FDG-PET/CT in non-small cell lung cancer diagnosis and staging in an Australian centre
BACKGROUND: Clinical practice guidelines and re-imbursement schedules vary in the recommended timing of FDG-PET/CT in the diagnostic evaluation of suspected or confirmed lung cancer. The aim was to estimate the probability of requiring more than one invasive test to complete diagnosis and staging in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252249/ https://www.ncbi.nlm.nih.gov/pubmed/34210303 http://dx.doi.org/10.1186/s12890-021-01564-w |
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author | Johnson, Anne Norman, Richard Piccolo, Francesco Manners, David |
author_facet | Johnson, Anne Norman, Richard Piccolo, Francesco Manners, David |
author_sort | Johnson, Anne |
collection | PubMed |
description | BACKGROUND: Clinical practice guidelines and re-imbursement schedules vary in the recommended timing of FDG-PET/CT in the diagnostic evaluation of suspected or confirmed lung cancer. The aim was to estimate the probability of requiring more than one invasive test to complete diagnosis and staging in non-small cell lung cancer if FDG-PET/CT was used prior to initial biopsy (FDG-PET/CT First) compared to current Australian funding criteria (CT First). METHODS: Single-centre retrospective study of individuals with pathologically confirmed NSCLC without evidence of metastatic disease on baseline computed tomography (CT) of the chest. Decision tree analysis based on diagnosis and staging approaches estimated the probability of requiring more than one invasive biopsy. A Monte Carlo analysis with 1000 simulations was used to estimate decision tree precision. RESULTS: After exclusions, 115 patients were included with median (IQR) age of 71 (63–79) and 55.6% were male. The majority of cases were early stage (Stage I 43.5%, Stage II 19.1%) and adenocarcinoma (65.2%) histological subtype. The estimated probability of requiring more than one invasive biopsy with FDG-PET/CT prior was 0.12 compared to 0.19 when using the base case CT First scenario. Using the Monte Carlo analysis, the mean (95% CI) probability using the FDG-PET First approach was 0.15 (95%CI 0.12–0.20) versus 0.20 (95% CI 0.15–0.27) for the CT First approach. Only 7.8% had CT Chest-occult metastatic disease on FDG-PET that was accessible by percutaneous biopsy. CONCLUSION: FDG-PET/CT performed prior to initial biopsy may reduce the proportion of people with NSCLC who require more than one biopsy attempt, but the clinical significance and overall cost-utility requires evaluation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12890-021-01564-w. |
format | Online Article Text |
id | pubmed-8252249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82522492021-07-06 The optimal timing of FDG-PET/CT in non-small cell lung cancer diagnosis and staging in an Australian centre Johnson, Anne Norman, Richard Piccolo, Francesco Manners, David BMC Pulm Med Research BACKGROUND: Clinical practice guidelines and re-imbursement schedules vary in the recommended timing of FDG-PET/CT in the diagnostic evaluation of suspected or confirmed lung cancer. The aim was to estimate the probability of requiring more than one invasive test to complete diagnosis and staging in non-small cell lung cancer if FDG-PET/CT was used prior to initial biopsy (FDG-PET/CT First) compared to current Australian funding criteria (CT First). METHODS: Single-centre retrospective study of individuals with pathologically confirmed NSCLC without evidence of metastatic disease on baseline computed tomography (CT) of the chest. Decision tree analysis based on diagnosis and staging approaches estimated the probability of requiring more than one invasive biopsy. A Monte Carlo analysis with 1000 simulations was used to estimate decision tree precision. RESULTS: After exclusions, 115 patients were included with median (IQR) age of 71 (63–79) and 55.6% were male. The majority of cases were early stage (Stage I 43.5%, Stage II 19.1%) and adenocarcinoma (65.2%) histological subtype. The estimated probability of requiring more than one invasive biopsy with FDG-PET/CT prior was 0.12 compared to 0.19 when using the base case CT First scenario. Using the Monte Carlo analysis, the mean (95% CI) probability using the FDG-PET First approach was 0.15 (95%CI 0.12–0.20) versus 0.20 (95% CI 0.15–0.27) for the CT First approach. Only 7.8% had CT Chest-occult metastatic disease on FDG-PET that was accessible by percutaneous biopsy. CONCLUSION: FDG-PET/CT performed prior to initial biopsy may reduce the proportion of people with NSCLC who require more than one biopsy attempt, but the clinical significance and overall cost-utility requires evaluation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12890-021-01564-w. BioMed Central 2021-07-01 /pmc/articles/PMC8252249/ /pubmed/34210303 http://dx.doi.org/10.1186/s12890-021-01564-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Johnson, Anne Norman, Richard Piccolo, Francesco Manners, David The optimal timing of FDG-PET/CT in non-small cell lung cancer diagnosis and staging in an Australian centre |
title | The optimal timing of FDG-PET/CT in non-small cell lung cancer diagnosis and staging in an Australian centre |
title_full | The optimal timing of FDG-PET/CT in non-small cell lung cancer diagnosis and staging in an Australian centre |
title_fullStr | The optimal timing of FDG-PET/CT in non-small cell lung cancer diagnosis and staging in an Australian centre |
title_full_unstemmed | The optimal timing of FDG-PET/CT in non-small cell lung cancer diagnosis and staging in an Australian centre |
title_short | The optimal timing of FDG-PET/CT in non-small cell lung cancer diagnosis and staging in an Australian centre |
title_sort | optimal timing of fdg-pet/ct in non-small cell lung cancer diagnosis and staging in an australian centre |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252249/ https://www.ncbi.nlm.nih.gov/pubmed/34210303 http://dx.doi.org/10.1186/s12890-021-01564-w |
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