Cargando…
Advantages of multi-arm non-randomised sequentially allocated cohort designs for Phase II oncology trials
BACKGROUND: Efficient trial designs are required to prioritise promising drugs within Phase II trials. Adaptive designs are examples of such designs, but their efficiency is reduced if there is a delay in assessing patient responses to treatment. METHODS: Motivated by the WIRE trial in renal cell ca...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770479/ https://www.ncbi.nlm.nih.gov/pubmed/34750494 http://dx.doi.org/10.1038/s41416-021-01613-5 |
_version_ | 1784635382516678656 |
---|---|
author | Mossop, Helen Grayling, Michael J. Gallagher, Ferdia A. Welsh, Sarah J. Stewart, Grant D. Wason, James M. S. |
author_facet | Mossop, Helen Grayling, Michael J. Gallagher, Ferdia A. Welsh, Sarah J. Stewart, Grant D. Wason, James M. S. |
author_sort | Mossop, Helen |
collection | PubMed |
description | BACKGROUND: Efficient trial designs are required to prioritise promising drugs within Phase II trials. Adaptive designs are examples of such designs, but their efficiency is reduced if there is a delay in assessing patient responses to treatment. METHODS: Motivated by the WIRE trial in renal cell carcinoma (NCT03741426), we compare three trial approaches to testing multiple treatment arms: (1) single-arm trials in sequence with interim analyses; (2) a parallel multi-arm multi-stage trial and (3) the design used in WIRE, which we call the Multi-Arm Sequential Trial with Efficient Recruitment (MASTER) design. The MASTER design recruits patients to one arm at a time, pausing recruitment to an arm when it has recruited the required number for an interim analysis. We conduct a simulation study to compare how long the three different trial designs take to evaluate a number of new treatment arms. RESULTS: The parallel multi-arm multi-stage and the MASTER design are much more efficient than separate trials. The MASTER design provides extra efficiency when there is endpoint delay, or recruitment is very quick. CONCLUSIONS: We recommend the MASTER design as an efficient way of testing multiple promising cancer treatments in non-comparative Phase II trials. |
format | Online Article Text |
id | pubmed-8770479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87704792022-02-04 Advantages of multi-arm non-randomised sequentially allocated cohort designs for Phase II oncology trials Mossop, Helen Grayling, Michael J. Gallagher, Ferdia A. Welsh, Sarah J. Stewart, Grant D. Wason, James M. S. Br J Cancer Article BACKGROUND: Efficient trial designs are required to prioritise promising drugs within Phase II trials. Adaptive designs are examples of such designs, but their efficiency is reduced if there is a delay in assessing patient responses to treatment. METHODS: Motivated by the WIRE trial in renal cell carcinoma (NCT03741426), we compare three trial approaches to testing multiple treatment arms: (1) single-arm trials in sequence with interim analyses; (2) a parallel multi-arm multi-stage trial and (3) the design used in WIRE, which we call the Multi-Arm Sequential Trial with Efficient Recruitment (MASTER) design. The MASTER design recruits patients to one arm at a time, pausing recruitment to an arm when it has recruited the required number for an interim analysis. We conduct a simulation study to compare how long the three different trial designs take to evaluate a number of new treatment arms. RESULTS: The parallel multi-arm multi-stage and the MASTER design are much more efficient than separate trials. The MASTER design provides extra efficiency when there is endpoint delay, or recruitment is very quick. CONCLUSIONS: We recommend the MASTER design as an efficient way of testing multiple promising cancer treatments in non-comparative Phase II trials. Nature Publishing Group UK 2021-11-08 2022-02-01 /pmc/articles/PMC8770479/ /pubmed/34750494 http://dx.doi.org/10.1038/s41416-021-01613-5 Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Mossop, Helen Grayling, Michael J. Gallagher, Ferdia A. Welsh, Sarah J. Stewart, Grant D. Wason, James M. S. Advantages of multi-arm non-randomised sequentially allocated cohort designs for Phase II oncology trials |
title | Advantages of multi-arm non-randomised sequentially allocated cohort designs for Phase II oncology trials |
title_full | Advantages of multi-arm non-randomised sequentially allocated cohort designs for Phase II oncology trials |
title_fullStr | Advantages of multi-arm non-randomised sequentially allocated cohort designs for Phase II oncology trials |
title_full_unstemmed | Advantages of multi-arm non-randomised sequentially allocated cohort designs for Phase II oncology trials |
title_short | Advantages of multi-arm non-randomised sequentially allocated cohort designs for Phase II oncology trials |
title_sort | advantages of multi-arm non-randomised sequentially allocated cohort designs for phase ii oncology trials |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770479/ https://www.ncbi.nlm.nih.gov/pubmed/34750494 http://dx.doi.org/10.1038/s41416-021-01613-5 |
work_keys_str_mv | AT mossophelen advantagesofmultiarmnonrandomisedsequentiallyallocatedcohortdesignsforphaseiioncologytrials AT graylingmichaelj advantagesofmultiarmnonrandomisedsequentiallyallocatedcohortdesignsforphaseiioncologytrials AT gallagherferdiaa advantagesofmultiarmnonrandomisedsequentiallyallocatedcohortdesignsforphaseiioncologytrials AT welshsarahj advantagesofmultiarmnonrandomisedsequentiallyallocatedcohortdesignsforphaseiioncologytrials AT stewartgrantd advantagesofmultiarmnonrandomisedsequentiallyallocatedcohortdesignsforphaseiioncologytrials AT wasonjamesms advantagesofmultiarmnonrandomisedsequentiallyallocatedcohortdesignsforphaseiioncologytrials |