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A multi-centre randomized controlled trial investigating Consolidation Chemotherapy with and without oxaliplatin in distal rectal cancer and Watch & Wait

BACKGROUND: Neoadjuvant chemoradiation(nCRT) has been considered the preferred initial treatment strategy for distal rectal cancer. Advantages of this approach include improved local control after radical surgery but also the opportunity for organ preserving strategies (Watch and Wait-WW). Consolida...

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Autores principales: Habr-Gama, Angelita, São Julião, Guilherme Pagin, Ortega, Cinthia D., Vailati, Bruna Borba, Araujo, Sergio, Jorge, Thiago, Sabbaga, Jorge, Rossi, Gustavo L., D’Alpino, Renata, Kater, Fabio Roberto, Aguilar, Patricia Bailão, Mattacheo, Adrian, Perez, Rodrigo Oliva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10268479/
https://www.ncbi.nlm.nih.gov/pubmed/37316784
http://dx.doi.org/10.1186/s12885-023-10984-2
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author Habr-Gama, Angelita
São Julião, Guilherme Pagin
Ortega, Cinthia D.
Vailati, Bruna Borba
Araujo, Sergio
Jorge, Thiago
Sabbaga, Jorge
Rossi, Gustavo L.
D’Alpino, Renata
Kater, Fabio Roberto
Aguilar, Patricia Bailão
Mattacheo, Adrian
Perez, Rodrigo Oliva
author_facet Habr-Gama, Angelita
São Julião, Guilherme Pagin
Ortega, Cinthia D.
Vailati, Bruna Borba
Araujo, Sergio
Jorge, Thiago
Sabbaga, Jorge
Rossi, Gustavo L.
D’Alpino, Renata
Kater, Fabio Roberto
Aguilar, Patricia Bailão
Mattacheo, Adrian
Perez, Rodrigo Oliva
author_sort Habr-Gama, Angelita
collection PubMed
description BACKGROUND: Neoadjuvant chemoradiation(nCRT) has been considered the preferred initial treatment strategy for distal rectal cancer. Advantages of this approach include improved local control after radical surgery but also the opportunity for organ preserving strategies (Watch and Wait-WW). Consolidation chemotherapy(cCT) regimens using fluoropyrimidine-based with or without oxalipatin following nCRT have demonstrated to increase complete response and organ preservation rates among these patients. However, the benefit of adding oxaliplatin to cCT compared to fluoropirimidine alone regimens in terms of primary tumor response remains unclear. Since oxalipatin-treatment may be associated with considerable toxicity, it becomes imperative to understand the benefit of its incorporation into standard cCT regimens in terms of primary tumor response. The aim of the present trial is to compare the outcomes of 2 different cCT regimens following nCRT (fluoropyrimidine-alone versus fluoropyrimidine + oxaliplatin) for patients with distal rectal cancer. METHODS: In this multi-centre study, patients with magnetic resonance-defined distal rectal tumors will be randomized on a 1:1 ratio to receive long-course chemoradiation (54 Gy) followed by cCT with fluoropyrimidine alone versus fluoropyrimidine + oxaliplatin. Magnetic resonance(MR) will be analyzed centrally prior to patient inclusion and randomization. mrT2-3N0-1 tumor located no more than 1 cm above the anorectal ring determined by sagittal views on MR will be eligible for the study. Tumor response will be assessed after 12 weeks from radiotherapy(RT) completion. Patients with clinical complete response (clinical, endoscopic and radiological) may be enrolled in an organ-preservation program(WW). The primary endpoint of this trial is decision to organ-preservation surveillance (WW) at 18 weeks from RT completion. Secondary endpoints are 3-year surgery-free survival, TME-free survival, distant metastases-free survival, local regrowth-free survival and colostomy-free survival. DISCUSSION: Long-course nCRT with cCT is associated with improved complete response rates and may be a very attractive alternative to increase the chances for organ-preservation strategies. Fluoropyrimidine-based cCT with or without oxaliplatin has never been investigated in the setting of a randomized trial to compare clinical response rates and the possibility of organ-preservation. The outcomes of this study may significantly impact clinical practice of patients with distal rectal cancer interested in organ-preservation. TRIAL REGISTRATION: www.clinicaltrials.gov NCT05000697; registered on August 11(th), 2021.
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spelling pubmed-102684792023-06-15 A multi-centre randomized controlled trial investigating Consolidation Chemotherapy with and without oxaliplatin in distal rectal cancer and Watch & Wait Habr-Gama, Angelita São Julião, Guilherme Pagin Ortega, Cinthia D. Vailati, Bruna Borba Araujo, Sergio Jorge, Thiago Sabbaga, Jorge Rossi, Gustavo L. D’Alpino, Renata Kater, Fabio Roberto Aguilar, Patricia Bailão Mattacheo, Adrian Perez, Rodrigo Oliva BMC Cancer Study Protocol BACKGROUND: Neoadjuvant chemoradiation(nCRT) has been considered the preferred initial treatment strategy for distal rectal cancer. Advantages of this approach include improved local control after radical surgery but also the opportunity for organ preserving strategies (Watch and Wait-WW). Consolidation chemotherapy(cCT) regimens using fluoropyrimidine-based with or without oxalipatin following nCRT have demonstrated to increase complete response and organ preservation rates among these patients. However, the benefit of adding oxaliplatin to cCT compared to fluoropirimidine alone regimens in terms of primary tumor response remains unclear. Since oxalipatin-treatment may be associated with considerable toxicity, it becomes imperative to understand the benefit of its incorporation into standard cCT regimens in terms of primary tumor response. The aim of the present trial is to compare the outcomes of 2 different cCT regimens following nCRT (fluoropyrimidine-alone versus fluoropyrimidine + oxaliplatin) for patients with distal rectal cancer. METHODS: In this multi-centre study, patients with magnetic resonance-defined distal rectal tumors will be randomized on a 1:1 ratio to receive long-course chemoradiation (54 Gy) followed by cCT with fluoropyrimidine alone versus fluoropyrimidine + oxaliplatin. Magnetic resonance(MR) will be analyzed centrally prior to patient inclusion and randomization. mrT2-3N0-1 tumor located no more than 1 cm above the anorectal ring determined by sagittal views on MR will be eligible for the study. Tumor response will be assessed after 12 weeks from radiotherapy(RT) completion. Patients with clinical complete response (clinical, endoscopic and radiological) may be enrolled in an organ-preservation program(WW). The primary endpoint of this trial is decision to organ-preservation surveillance (WW) at 18 weeks from RT completion. Secondary endpoints are 3-year surgery-free survival, TME-free survival, distant metastases-free survival, local regrowth-free survival and colostomy-free survival. DISCUSSION: Long-course nCRT with cCT is associated with improved complete response rates and may be a very attractive alternative to increase the chances for organ-preservation strategies. Fluoropyrimidine-based cCT with or without oxaliplatin has never been investigated in the setting of a randomized trial to compare clinical response rates and the possibility of organ-preservation. The outcomes of this study may significantly impact clinical practice of patients with distal rectal cancer interested in organ-preservation. TRIAL REGISTRATION: www.clinicaltrials.gov NCT05000697; registered on August 11(th), 2021. BioMed Central 2023-06-14 /pmc/articles/PMC10268479/ /pubmed/37316784 http://dx.doi.org/10.1186/s12885-023-10984-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Study Protocol
Habr-Gama, Angelita
São Julião, Guilherme Pagin
Ortega, Cinthia D.
Vailati, Bruna Borba
Araujo, Sergio
Jorge, Thiago
Sabbaga, Jorge
Rossi, Gustavo L.
D’Alpino, Renata
Kater, Fabio Roberto
Aguilar, Patricia Bailão
Mattacheo, Adrian
Perez, Rodrigo Oliva
A multi-centre randomized controlled trial investigating Consolidation Chemotherapy with and without oxaliplatin in distal rectal cancer and Watch & Wait
title A multi-centre randomized controlled trial investigating Consolidation Chemotherapy with and without oxaliplatin in distal rectal cancer and Watch & Wait
title_full A multi-centre randomized controlled trial investigating Consolidation Chemotherapy with and without oxaliplatin in distal rectal cancer and Watch & Wait
title_fullStr A multi-centre randomized controlled trial investigating Consolidation Chemotherapy with and without oxaliplatin in distal rectal cancer and Watch & Wait
title_full_unstemmed A multi-centre randomized controlled trial investigating Consolidation Chemotherapy with and without oxaliplatin in distal rectal cancer and Watch & Wait
title_short A multi-centre randomized controlled trial investigating Consolidation Chemotherapy with and without oxaliplatin in distal rectal cancer and Watch & Wait
title_sort multi-centre randomized controlled trial investigating consolidation chemotherapy with and without oxaliplatin in distal rectal cancer and watch & wait
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10268479/
https://www.ncbi.nlm.nih.gov/pubmed/37316784
http://dx.doi.org/10.1186/s12885-023-10984-2
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