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 carc...

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Vydáno v:British journal of cancer Ročník 126; číslo 2; s. 204 - 210
Hlavní autoři: Mossop, Helen, Grayling, Michael J., Gallagher, Ferdia A., Welsh, Sarah J., Stewart, Grant D., Wason, James M. S.
Médium: Journal Article
Jazyk:angličtina
Vydáno: London Nature Publishing Group UK 01.02.2022
Nature Publishing Group
Témata:
692/308/2779/109/2425
692/308/2779/777
Adaptive Clinical Trials as Topic - methods
Biomedical and Life Sciences
Biomedicine
Cancer Research
Cancer therapies
Clinical trials
Clinical Trials, Phase II as Topic - methods
Cohort Studies
Computer Simulation - standards
Drug Resistance
Efficiency
Epidemiology
Humans
Hypotheses
Kidney cancer
Medical Oncology - methods
Molecular Medicine
Neoplasms - drug therapy
Neoplasms - pathology
Non-Randomized Controlled Trials as Topic - methods
Oncology
Patients
Recruitment
Renal cell carcinoma
Research Design - standards
Response rates
Sample Size
Simulation
Surgery
Treatment Outcome
ISSN:0007-0920, 1532-1827, 1532-1827
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Shrnutí: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.
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ISSN:0007-0920
1532-1827
1532-1827
DOI:10.1038/s41416-021-01613-5