Advantages of multi-arm non-randomised sequentially allocated cohort designs for Phase II oncology trials.
dc.contributor.author | Mossop, Helen | |
dc.contributor.author | Grayling, Michael J | |
dc.contributor.author | Gallagher, Ferdia | |
dc.contributor.author | Welsh, Sarah | |
dc.contributor.author | Stewart, Grant | |
dc.contributor.author | Wason, James MS | |
dc.date.accessioned | 2021-10-20T23:30:17Z | |
dc.date.available | 2021-10-20T23:30:17Z | |
dc.date.issued | 2021-11-08 | |
dc.identifier.issn | 0007-0920 | |
dc.identifier.uri | https://www.repository.cam.ac.uk/handle/1810/329684 | |
dc.description.abstract | 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. | |
dc.description.sponsorship | Cancer Research UK Cambridge Centre [C9685/A25177] | |
dc.language | eng | |
dc.publisher | Springer Science and Business Media LLC | |
dc.rights | All rights reserved | |
dc.rights.uri | http://www.rioxx.net/licenses/all-rights-reserved | |
dc.title | Advantages of multi-arm non-randomised sequentially allocated cohort designs for Phase II oncology trials. | |
dc.type | Article | |
prism.publicationDate | 2021 | |
prism.publicationName | Br J Cancer | |
dc.identifier.doi | 10.17863/CAM.77130 | |
dcterms.dateAccepted | 2021-10-21 | |
rioxxterms.versionofrecord | 10.1038/s41416-021-01613-5 | |
rioxxterms.version | AM | |
rioxxterms.licenseref.uri | http://www.rioxx.net/licenses/all-rights-reserved | |
rioxxterms.licenseref.startdate | 2021-11-08 | |
dc.contributor.orcid | Grayling, Michael J [0000-0002-0680-6668] | |
dc.contributor.orcid | Gallagher, Ferdia [0000-0003-4784-5230] | |
dc.contributor.orcid | Welsh, Sarah [0000-0001-5690-2677] | |
dc.contributor.orcid | Stewart, Grant [0000-0003-3188-9140] | |
dc.contributor.orcid | Wason, James MS [0000-0002-4691-126X] | |
dc.identifier.eissn | 1532-1827 | |
rioxxterms.type | Journal Article/Review | |
pubs.funder-project-id | MRC (MR/T024097/1) | |
pubs.funder-project-id | Cancer Research UK (C96/A25177) | |
cam.issuedOnline | 2021-11-08 | |
cam.orpheus.success | Mon Nov 22 07:30:40 GMT 2021 - Embargo updated | |
cam.orpheus.counter | 4 | |
rioxxterms.freetoread.startdate | 2022-05-08 |
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