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Translation of IDEA trial results into clinical practice: Analysis of the implementation of a new guideline for colon cancer

The IDEA trial showed no clinical relevant differences in efficacy between 3 and 6 months of oxaliplatin‐based adjuvant chemotherapy (ACT) in colon cancer (CC), while toxicity was substantially lower in the 3 months regimen. Therefore, in 2017 the Dutch colorectal cancer guideline was revised and cu...

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Autores principales: van Rooijen, Karlijn L., Derksen, Jeroen W. G., Verkooijen, Helena M., Vink, Geraldine R., Koopman, Miriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545923/
https://www.ncbi.nlm.nih.gov/pubmed/35657640
http://dx.doi.org/10.1002/ijc.34149
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author van Rooijen, Karlijn L.
Derksen, Jeroen W. G.
Verkooijen, Helena M.
Vink, Geraldine R.
Koopman, Miriam
author_facet van Rooijen, Karlijn L.
Derksen, Jeroen W. G.
Verkooijen, Helena M.
Vink, Geraldine R.
Koopman, Miriam
author_sort van Rooijen, Karlijn L.
collection PubMed
description The IDEA trial showed no clinical relevant differences in efficacy between 3 and 6 months of oxaliplatin‐based adjuvant chemotherapy (ACT) in colon cancer (CC), while toxicity was substantially lower in the 3 months regimen. Therefore, in 2017 the Dutch colorectal cancer guideline was revised and currently recommends 3 months of oxaliplatin‐based ACT. Furthermore, the definition of high‐risk stage II CC was restricted to pT4 tumors. We analyzed changes in ACT between 2015 and 2019. From the Netherlands Cancer Registry all 16 721 patients ≥18 years with resected high‐risk stage II and stage III CC during 2015 to 2019 were selected. Differences in patient and treatment characteristics were analyzed per calendar year according to stage and age. Mean duration of oxaliplatin‐based ACT decreased from 18.6 (±8.0) to 9.5 (±3.8) weeks between 2015 and 2019. In patients receiving ACT (n = 8170), the proportion treated with oxaliplatin increased from 74% to 83%. The proportion of patients receiving ACT was stable, 61% to 69% in stage III and 26% to 29% in pT4 stage II. ACT in previous high‐risk pT3N0 disease decreased from 15% to 3%. Use of oxaliplatin increased from 27% to 49% in patients aged ≥75 years. The revised guideline was rapidly implemented and led to an increase in oxaliplatin‐based ACT in the elderly and increased guideline‐adherence in high‐risk stage II CC.
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spelling pubmed-95459232022-10-14 Translation of IDEA trial results into clinical practice: Analysis of the implementation of a new guideline for colon cancer van Rooijen, Karlijn L. Derksen, Jeroen W. G. Verkooijen, Helena M. Vink, Geraldine R. Koopman, Miriam Int J Cancer Cancer Epidemiology The IDEA trial showed no clinical relevant differences in efficacy between 3 and 6 months of oxaliplatin‐based adjuvant chemotherapy (ACT) in colon cancer (CC), while toxicity was substantially lower in the 3 months regimen. Therefore, in 2017 the Dutch colorectal cancer guideline was revised and currently recommends 3 months of oxaliplatin‐based ACT. Furthermore, the definition of high‐risk stage II CC was restricted to pT4 tumors. We analyzed changes in ACT between 2015 and 2019. From the Netherlands Cancer Registry all 16 721 patients ≥18 years with resected high‐risk stage II and stage III CC during 2015 to 2019 were selected. Differences in patient and treatment characteristics were analyzed per calendar year according to stage and age. Mean duration of oxaliplatin‐based ACT decreased from 18.6 (±8.0) to 9.5 (±3.8) weeks between 2015 and 2019. In patients receiving ACT (n = 8170), the proportion treated with oxaliplatin increased from 74% to 83%. The proportion of patients receiving ACT was stable, 61% to 69% in stage III and 26% to 29% in pT4 stage II. ACT in previous high‐risk pT3N0 disease decreased from 15% to 3%. Use of oxaliplatin increased from 27% to 49% in patients aged ≥75 years. The revised guideline was rapidly implemented and led to an increase in oxaliplatin‐based ACT in the elderly and increased guideline‐adherence in high‐risk stage II CC. John Wiley & Sons, Inc. 2022-06-21 2022-10-15 /pmc/articles/PMC9545923/ /pubmed/35657640 http://dx.doi.org/10.1002/ijc.34149 Text en © 2022 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Cancer Epidemiology
van Rooijen, Karlijn L.
Derksen, Jeroen W. G.
Verkooijen, Helena M.
Vink, Geraldine R.
Koopman, Miriam
Translation of IDEA trial results into clinical practice: Analysis of the implementation of a new guideline for colon cancer
title Translation of IDEA trial results into clinical practice: Analysis of the implementation of a new guideline for colon cancer
title_full Translation of IDEA trial results into clinical practice: Analysis of the implementation of a new guideline for colon cancer
title_fullStr Translation of IDEA trial results into clinical practice: Analysis of the implementation of a new guideline for colon cancer
title_full_unstemmed Translation of IDEA trial results into clinical practice: Analysis of the implementation of a new guideline for colon cancer
title_short Translation of IDEA trial results into clinical practice: Analysis of the implementation of a new guideline for colon cancer
title_sort translation of idea trial results into clinical practice: analysis of the implementation of a new guideline for colon cancer
topic Cancer Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545923/
https://www.ncbi.nlm.nih.gov/pubmed/35657640
http://dx.doi.org/10.1002/ijc.34149
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