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PROPERTY: study protocol for a randomized, double-blind, multicenter placebo-controlled trial assessing neurotoxicity in patients with metastatic gastrointestinal cancer taking PHYCOCARE® during oxaliplatin-based chemotherapy

BACKGROUND: Chemotherapy-induced peripheral neuropathy (CIPN) is one of the most common adverse effects of antineoplastic agents, ranging in prevalence from 19% to over 85%. Clinically, CIPN is a predominantly sensory neuropathy that may be accompanied by motor and autonomic changes of varying inten...

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Autores principales: Le Gouill-Jaijarat, Christele, Péréon, Yann, Leroy, Maxime, Lépine, Olivier, Loloum, Aymeric, Peluchon, Claire, Volteau, Christelle, Martineau, Anne-Sophie, Korner, Simon, Perrault, Caroline, Benmaziane, Asmahane, Girot, Paul, Petorin, Caroline, Perret, Clément, Ligeza-Poisson, Catherine, Mayeur, Didier, Flet, Laurent, Chiffoleau, Anne, Poinas, Alexandra, Bennouna, Jaafar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854012/
https://www.ncbi.nlm.nih.gov/pubmed/36670495
http://dx.doi.org/10.1186/s13063-023-07071-z
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author Le Gouill-Jaijarat, Christele
Péréon, Yann
Leroy, Maxime
Lépine, Olivier
Loloum, Aymeric
Peluchon, Claire
Volteau, Christelle
Martineau, Anne-Sophie
Korner, Simon
Perrault, Caroline
Benmaziane, Asmahane
Girot, Paul
Petorin, Caroline
Perret, Clément
Ligeza-Poisson, Catherine
Mayeur, Didier
Flet, Laurent
Chiffoleau, Anne
Poinas, Alexandra
Bennouna, Jaafar
author_facet Le Gouill-Jaijarat, Christele
Péréon, Yann
Leroy, Maxime
Lépine, Olivier
Loloum, Aymeric
Peluchon, Claire
Volteau, Christelle
Martineau, Anne-Sophie
Korner, Simon
Perrault, Caroline
Benmaziane, Asmahane
Girot, Paul
Petorin, Caroline
Perret, Clément
Ligeza-Poisson, Catherine
Mayeur, Didier
Flet, Laurent
Chiffoleau, Anne
Poinas, Alexandra
Bennouna, Jaafar
author_sort Le Gouill-Jaijarat, Christele
collection PubMed
description BACKGROUND: Chemotherapy-induced peripheral neuropathy (CIPN) is one of the most common adverse effects of antineoplastic agents, ranging in prevalence from 19% to over 85%. Clinically, CIPN is a predominantly sensory neuropathy that may be accompanied by motor and autonomic changes of varying intensity and duration. The high prevalence of CIPN among cancer patients makes it a major problem for both patients and survivors, as well as for their health care providers, especially because there is currently no single effective method of preventing CIPN; moreover, the options for treating this syndrome are very limited. Phycocyanin, a biliprotein pigment and an important constituent of the blue-green algae Spirulina platensis, has been reported to possess significant antioxidant and radical-scavenging properties, offering protection against oxidative stress, which is one of the hypothetic mechanisms, between others, of CIPN occurrence. METHODS: Our hypothesis is that phycocyanin may give protection against oxaliplatin-induced neuropathy in the treatment of gastrointestinal cancers. Our trial will be a randomized double-blind placebo-controlled study with 110 randomized patients suffering from metastatic gastrointestinal adenocarcinoma including esogastric, colorectal, and pancreatic cancers. Patients are being followed up in the gastroenterology or oncology departments of seven French hospitals. DISCUSSION: Due to the neuropathy, patients need to avoid injury by paying careful attention to home safety; patients’ physicians often prescribe over-the-counter pain medications. If validated, our hypothesis should help to limit neurotoxicity without the need to discontinue chemotherapy. TRIAL REGISTRATION: ClinicalTrials.gov NCT05025826. First published on August 27, 2021. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13063-023-07071-z.
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spelling pubmed-98540122023-01-21 PROPERTY: study protocol for a randomized, double-blind, multicenter placebo-controlled trial assessing neurotoxicity in patients with metastatic gastrointestinal cancer taking PHYCOCARE® during oxaliplatin-based chemotherapy Le Gouill-Jaijarat, Christele Péréon, Yann Leroy, Maxime Lépine, Olivier Loloum, Aymeric Peluchon, Claire Volteau, Christelle Martineau, Anne-Sophie Korner, Simon Perrault, Caroline Benmaziane, Asmahane Girot, Paul Petorin, Caroline Perret, Clément Ligeza-Poisson, Catherine Mayeur, Didier Flet, Laurent Chiffoleau, Anne Poinas, Alexandra Bennouna, Jaafar Trials Study Protocol BACKGROUND: Chemotherapy-induced peripheral neuropathy (CIPN) is one of the most common adverse effects of antineoplastic agents, ranging in prevalence from 19% to over 85%. Clinically, CIPN is a predominantly sensory neuropathy that may be accompanied by motor and autonomic changes of varying intensity and duration. The high prevalence of CIPN among cancer patients makes it a major problem for both patients and survivors, as well as for their health care providers, especially because there is currently no single effective method of preventing CIPN; moreover, the options for treating this syndrome are very limited. Phycocyanin, a biliprotein pigment and an important constituent of the blue-green algae Spirulina platensis, has been reported to possess significant antioxidant and radical-scavenging properties, offering protection against oxidative stress, which is one of the hypothetic mechanisms, between others, of CIPN occurrence. METHODS: Our hypothesis is that phycocyanin may give protection against oxaliplatin-induced neuropathy in the treatment of gastrointestinal cancers. Our trial will be a randomized double-blind placebo-controlled study with 110 randomized patients suffering from metastatic gastrointestinal adenocarcinoma including esogastric, colorectal, and pancreatic cancers. Patients are being followed up in the gastroenterology or oncology departments of seven French hospitals. DISCUSSION: Due to the neuropathy, patients need to avoid injury by paying careful attention to home safety; patients’ physicians often prescribe over-the-counter pain medications. If validated, our hypothesis should help to limit neurotoxicity without the need to discontinue chemotherapy. TRIAL REGISTRATION: ClinicalTrials.gov NCT05025826. First published on August 27, 2021. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13063-023-07071-z. BioMed Central 2023-01-20 /pmc/articles/PMC9854012/ /pubmed/36670495 http://dx.doi.org/10.1186/s13063-023-07071-z Text en © The Author(s) 2023 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 Study Protocol
Le Gouill-Jaijarat, Christele
Péréon, Yann
Leroy, Maxime
Lépine, Olivier
Loloum, Aymeric
Peluchon, Claire
Volteau, Christelle
Martineau, Anne-Sophie
Korner, Simon
Perrault, Caroline
Benmaziane, Asmahane
Girot, Paul
Petorin, Caroline
Perret, Clément
Ligeza-Poisson, Catherine
Mayeur, Didier
Flet, Laurent
Chiffoleau, Anne
Poinas, Alexandra
Bennouna, Jaafar
PROPERTY: study protocol for a randomized, double-blind, multicenter placebo-controlled trial assessing neurotoxicity in patients with metastatic gastrointestinal cancer taking PHYCOCARE® during oxaliplatin-based chemotherapy
title PROPERTY: study protocol for a randomized, double-blind, multicenter placebo-controlled trial assessing neurotoxicity in patients with metastatic gastrointestinal cancer taking PHYCOCARE® during oxaliplatin-based chemotherapy
title_full PROPERTY: study protocol for a randomized, double-blind, multicenter placebo-controlled trial assessing neurotoxicity in patients with metastatic gastrointestinal cancer taking PHYCOCARE® during oxaliplatin-based chemotherapy
title_fullStr PROPERTY: study protocol for a randomized, double-blind, multicenter placebo-controlled trial assessing neurotoxicity in patients with metastatic gastrointestinal cancer taking PHYCOCARE® during oxaliplatin-based chemotherapy
title_full_unstemmed PROPERTY: study protocol for a randomized, double-blind, multicenter placebo-controlled trial assessing neurotoxicity in patients with metastatic gastrointestinal cancer taking PHYCOCARE® during oxaliplatin-based chemotherapy
title_short PROPERTY: study protocol for a randomized, double-blind, multicenter placebo-controlled trial assessing neurotoxicity in patients with metastatic gastrointestinal cancer taking PHYCOCARE® during oxaliplatin-based chemotherapy
title_sort property: study protocol for a randomized, double-blind, multicenter placebo-controlled trial assessing neurotoxicity in patients with metastatic gastrointestinal cancer taking phycocare® during oxaliplatin-based chemotherapy
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854012/
https://www.ncbi.nlm.nih.gov/pubmed/36670495
http://dx.doi.org/10.1186/s13063-023-07071-z
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