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Total neoadjuvant therapy in rectal cancer: a network meta-analysis of randomized trials

PURPOSE: To assess the efficacy of total neoadjuvant therapy (TNT) for rectal carcinoma in comparison with conventional chemoradiotherapy (CRT). METHODS: A systematic review was performed according to the PRISMA guidelines. A Bayesian network meta-analysis was done using NetMetaXL and WinBUGS. This...

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Autores principales: Sychev, Sergey, Ponomarenko, Aleksey, Chernyshov, Stanislav, Alekseev, Mikhail, Mamedli, Zaman, Kuzmichev, Dmitriy, Polynovskiy, Andrey, Rybakov, Evgeny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Coloproctology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10475801/
https://www.ncbi.nlm.nih.gov/pubmed/37038270
http://dx.doi.org/10.3393/ac.2022.00920.0131
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author Sychev, Sergey
Ponomarenko, Aleksey
Chernyshov, Stanislav
Alekseev, Mikhail
Mamedli, Zaman
Kuzmichev, Dmitriy
Polynovskiy, Andrey
Rybakov, Evgeny
author_facet Sychev, Sergey
Ponomarenko, Aleksey
Chernyshov, Stanislav
Alekseev, Mikhail
Mamedli, Zaman
Kuzmichev, Dmitriy
Polynovskiy, Andrey
Rybakov, Evgeny
author_sort Sychev, Sergey
collection PubMed
description PURPOSE: To assess the efficacy of total neoadjuvant therapy (TNT) for rectal carcinoma in comparison with conventional chemoradiotherapy (CRT). METHODS: A systematic review was performed according to the PRISMA guidelines. A Bayesian network meta-analysis was done using NetMetaXL and WinBUGS. This study was registered in PROSPERO on March 3, 2022 (No. CRD-42022307867). RESULTS: Outcomes of 2,719 patients from 10 randomized trials between 2010 and 2022 were selected. Of these 1,191 (44%) had conventional long-course CRT (50–54 Gy) and capecitabine, 506 (18%) had induction chemotherapy followed by CRT (50–54 Gy) and capecitabine (iTNT), 230 (9%) had long-course CRT (50–54 Gy) followed by consolidation chemotherapy (cTNT), and 792 (29%) undergone modified short-course radiotherapy (25 Gy) with subsequent chemotherapy (mTNT). Total pathologic complete response (pCR) was 20% in the iTNT group, 21% in the mTNT group, 22% in the cTNT group, and 12% in the CRT group. Statistically significant difference in pCR rates was detected when comparing iTNT with CRT (odds ratio [OR], 1.76; 95% credible interval [CrI], 1.06–2.8), mTNT with CRT (OR, 1.90; 95% CrI, 1.25–2.74), and cTNT with CRT groups (OR, 2.54; 95% CrI, 1.26–5.08). No differences were found in R0 resection rates. No significant difference was found in long-term outcomes. CONCLUSION: The early administration of systemic chemotherapy in the TNT regimen has improved short-term outcomes, though long-term results are underreported. Randomized trials with survival as the endpoint are necessary to evaluate the possible advantages of TNT modes.
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spelling pubmed-104758012023-09-05 Total neoadjuvant therapy in rectal cancer: a network meta-analysis of randomized trials Sychev, Sergey Ponomarenko, Aleksey Chernyshov, Stanislav Alekseev, Mikhail Mamedli, Zaman Kuzmichev, Dmitriy Polynovskiy, Andrey Rybakov, Evgeny Ann Coloproctol Review PURPOSE: To assess the efficacy of total neoadjuvant therapy (TNT) for rectal carcinoma in comparison with conventional chemoradiotherapy (CRT). METHODS: A systematic review was performed according to the PRISMA guidelines. A Bayesian network meta-analysis was done using NetMetaXL and WinBUGS. This study was registered in PROSPERO on March 3, 2022 (No. CRD-42022307867). RESULTS: Outcomes of 2,719 patients from 10 randomized trials between 2010 and 2022 were selected. Of these 1,191 (44%) had conventional long-course CRT (50–54 Gy) and capecitabine, 506 (18%) had induction chemotherapy followed by CRT (50–54 Gy) and capecitabine (iTNT), 230 (9%) had long-course CRT (50–54 Gy) followed by consolidation chemotherapy (cTNT), and 792 (29%) undergone modified short-course radiotherapy (25 Gy) with subsequent chemotherapy (mTNT). Total pathologic complete response (pCR) was 20% in the iTNT group, 21% in the mTNT group, 22% in the cTNT group, and 12% in the CRT group. Statistically significant difference in pCR rates was detected when comparing iTNT with CRT (odds ratio [OR], 1.76; 95% credible interval [CrI], 1.06–2.8), mTNT with CRT (OR, 1.90; 95% CrI, 1.25–2.74), and cTNT with CRT groups (OR, 2.54; 95% CrI, 1.26–5.08). No differences were found in R0 resection rates. No significant difference was found in long-term outcomes. CONCLUSION: The early administration of systemic chemotherapy in the TNT regimen has improved short-term outcomes, though long-term results are underreported. Randomized trials with survival as the endpoint are necessary to evaluate the possible advantages of TNT modes. Korean Society of Coloproctology 2023-08 2023-04-11 /pmc/articles/PMC10475801/ /pubmed/37038270 http://dx.doi.org/10.3393/ac.2022.00920.0131 Text en © 2023 Korean Society of Coloproctology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Sychev, Sergey
Ponomarenko, Aleksey
Chernyshov, Stanislav
Alekseev, Mikhail
Mamedli, Zaman
Kuzmichev, Dmitriy
Polynovskiy, Andrey
Rybakov, Evgeny
Total neoadjuvant therapy in rectal cancer: a network meta-analysis of randomized trials
title Total neoadjuvant therapy in rectal cancer: a network meta-analysis of randomized trials
title_full Total neoadjuvant therapy in rectal cancer: a network meta-analysis of randomized trials
title_fullStr Total neoadjuvant therapy in rectal cancer: a network meta-analysis of randomized trials
title_full_unstemmed Total neoadjuvant therapy in rectal cancer: a network meta-analysis of randomized trials
title_short Total neoadjuvant therapy in rectal cancer: a network meta-analysis of randomized trials
title_sort total neoadjuvant therapy in rectal cancer: a network meta-analysis of randomized trials
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10475801/
https://www.ncbi.nlm.nih.gov/pubmed/37038270
http://dx.doi.org/10.3393/ac.2022.00920.0131
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