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Combination Early-Phase Trials of Anticancer Agents in Children and Adolescents

There is an increasing need to evaluate innovative drugs for childhood cancer using combination strategies. Strong biological rationale and clinical experience suggest that multiple agents will be more efficacious than monotherapy for most diseases and may overcome resistance mechanisms and increase...

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Autores principales: Moreno, Lucas, DuBois, Steven G., Glade Bender, Julia, Mauguen, Audrey, Bird, Nick, Buenger, Vickie, Casanova, Michela, Doz, François, Fox, Elizabeth, Gore, Lia, Hawkins, Douglas S., Izraeli, Shai, Jones, David T.W., Kearns, Pamela R., Molenaar, Jan J., Nysom, Karsten, Pfister, Stefan, Reaman, Gregory, Smith, Malcolm, Weigel, Brenda, Vassal, Gilles, Zwaan, Christian Michel, Paoletti, Xavier, Iasonos, Alexia, Pearson, Andrew D.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10414747/
https://www.ncbi.nlm.nih.gov/pubmed/37015036
http://dx.doi.org/10.1200/JCO.22.02430
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author Moreno, Lucas
DuBois, Steven G.
Glade Bender, Julia
Mauguen, Audrey
Bird, Nick
Buenger, Vickie
Casanova, Michela
Doz, François
Fox, Elizabeth
Gore, Lia
Hawkins, Douglas S.
Izraeli, Shai
Jones, David T.W.
Kearns, Pamela R.
Molenaar, Jan J.
Nysom, Karsten
Pfister, Stefan
Reaman, Gregory
Smith, Malcolm
Weigel, Brenda
Vassal, Gilles
Zwaan, Christian Michel
Paoletti, Xavier
Iasonos, Alexia
Pearson, Andrew D.J.
author_facet Moreno, Lucas
DuBois, Steven G.
Glade Bender, Julia
Mauguen, Audrey
Bird, Nick
Buenger, Vickie
Casanova, Michela
Doz, François
Fox, Elizabeth
Gore, Lia
Hawkins, Douglas S.
Izraeli, Shai
Jones, David T.W.
Kearns, Pamela R.
Molenaar, Jan J.
Nysom, Karsten
Pfister, Stefan
Reaman, Gregory
Smith, Malcolm
Weigel, Brenda
Vassal, Gilles
Zwaan, Christian Michel
Paoletti, Xavier
Iasonos, Alexia
Pearson, Andrew D.J.
author_sort Moreno, Lucas
collection PubMed
description There is an increasing need to evaluate innovative drugs for childhood cancer using combination strategies. Strong biological rationale and clinical experience suggest that multiple agents will be more efficacious than monotherapy for most diseases and may overcome resistance mechanisms and increase synergy. The process to evaluate these combination trials needs to maximize efficiency and should be agreed by all stakeholders. METHODS: After a review of existing combination trial methodologies, regulatory requirements, and current results, a consensus among stakeholders was achieved. RESULTS: Combinations of anticancer therapies should be developed on the basis of mechanism of action and robust preclinical evaluation, and may include data from adult clinical trials. The general principle for combination early-phase studies is that, when possible, clinical trials should be dose- and schedule-confirmatory rather than dose-exploratory, and every effort should be made to optimize doses early. Efficient early-phase combination trials should be seamless, including dose confirmation and randomized expansion. Dose evaluation designs for combinations depend on the extent of previous knowledge. If not previously evaluated, limited evaluation of monotherapy should be included in the same clinical trial as the combination. Randomized evaluation of a new agent plus standard therapy versus standard therapy is the most effective approach to isolate the effect and toxicity of the novel agent. Platform trials may be valuable in the evaluation of combination studies. Patient advocates and regulators should be engaged with investigators early in a proposed clinical development pathway and trial design must consider regulatory requirements. CONCLUSION: An optimized, agreed approach to the design and evaluation of early-phase pediatric combination trials will accelerate drug development and benefit all stakeholders, most importantly children and adolescents with cancer.
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spelling pubmed-104147472023-08-11 Combination Early-Phase Trials of Anticancer Agents in Children and Adolescents Moreno, Lucas DuBois, Steven G. Glade Bender, Julia Mauguen, Audrey Bird, Nick Buenger, Vickie Casanova, Michela Doz, François Fox, Elizabeth Gore, Lia Hawkins, Douglas S. Izraeli, Shai Jones, David T.W. Kearns, Pamela R. Molenaar, Jan J. Nysom, Karsten Pfister, Stefan Reaman, Gregory Smith, Malcolm Weigel, Brenda Vassal, Gilles Zwaan, Christian Michel Paoletti, Xavier Iasonos, Alexia Pearson, Andrew D.J. J Clin Oncol Special Articles There is an increasing need to evaluate innovative drugs for childhood cancer using combination strategies. Strong biological rationale and clinical experience suggest that multiple agents will be more efficacious than monotherapy for most diseases and may overcome resistance mechanisms and increase synergy. The process to evaluate these combination trials needs to maximize efficiency and should be agreed by all stakeholders. METHODS: After a review of existing combination trial methodologies, regulatory requirements, and current results, a consensus among stakeholders was achieved. RESULTS: Combinations of anticancer therapies should be developed on the basis of mechanism of action and robust preclinical evaluation, and may include data from adult clinical trials. The general principle for combination early-phase studies is that, when possible, clinical trials should be dose- and schedule-confirmatory rather than dose-exploratory, and every effort should be made to optimize doses early. Efficient early-phase combination trials should be seamless, including dose confirmation and randomized expansion. Dose evaluation designs for combinations depend on the extent of previous knowledge. If not previously evaluated, limited evaluation of monotherapy should be included in the same clinical trial as the combination. Randomized evaluation of a new agent plus standard therapy versus standard therapy is the most effective approach to isolate the effect and toxicity of the novel agent. Platform trials may be valuable in the evaluation of combination studies. Patient advocates and regulators should be engaged with investigators early in a proposed clinical development pathway and trial design must consider regulatory requirements. CONCLUSION: An optimized, agreed approach to the design and evaluation of early-phase pediatric combination trials will accelerate drug development and benefit all stakeholders, most importantly children and adolescents with cancer. Wolters Kluwer Health 2023-06-20 2023-04-04 /pmc/articles/PMC10414747/ /pubmed/37015036 http://dx.doi.org/10.1200/JCO.22.02430 Text en © 2023 by American Society of Clinical Oncology https://creativecommons.org/licenses/by-nc-nd/4.0/Creative Commons Attribution Non-Commercial No Derivatives 4.0 License: https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Special Articles
Moreno, Lucas
DuBois, Steven G.
Glade Bender, Julia
Mauguen, Audrey
Bird, Nick
Buenger, Vickie
Casanova, Michela
Doz, François
Fox, Elizabeth
Gore, Lia
Hawkins, Douglas S.
Izraeli, Shai
Jones, David T.W.
Kearns, Pamela R.
Molenaar, Jan J.
Nysom, Karsten
Pfister, Stefan
Reaman, Gregory
Smith, Malcolm
Weigel, Brenda
Vassal, Gilles
Zwaan, Christian Michel
Paoletti, Xavier
Iasonos, Alexia
Pearson, Andrew D.J.
Combination Early-Phase Trials of Anticancer Agents in Children and Adolescents
title Combination Early-Phase Trials of Anticancer Agents in Children and Adolescents
title_full Combination Early-Phase Trials of Anticancer Agents in Children and Adolescents
title_fullStr Combination Early-Phase Trials of Anticancer Agents in Children and Adolescents
title_full_unstemmed Combination Early-Phase Trials of Anticancer Agents in Children and Adolescents
title_short Combination Early-Phase Trials of Anticancer Agents in Children and Adolescents
title_sort combination early-phase trials of anticancer agents in children and adolescents
topic Special Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10414747/
https://www.ncbi.nlm.nih.gov/pubmed/37015036
http://dx.doi.org/10.1200/JCO.22.02430
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