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dc.contributor.authorPopat, S
dc.contributor.authorLiu, SV
dc.contributor.authorScheuer, N
dc.contributor.authorHsu, GG
dc.contributor.authorLockhart, A
dc.contributor.authorRamagopalan, SV
dc.contributor.authorGriesinger, F
dc.contributor.authorSubbiah, V
dc.coverage.spatialEngland
dc.date.accessioned2022-09-06T13:07:34Z
dc.date.available2022-09-06T13:07:34Z
dc.date.issued2022-06-17
dc.identifierARTN 3500
dc.identifier10.1038/s41467-022-30908-1
dc.identifier.citationNature Communications, 2022, 13 (1), pp. 3500 -en_US
dc.identifier.issn2041-1723
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5428
dc.identifier.eissn2041-1723
dc.identifier.eissn2041-1723
dc.identifier.doi10.1038/s41467-022-30908-1
dc.description.abstractAs advanced non-small cell lung cancer (aNSCLC) is being increasingly divided into rare oncogene-driven subsets, conducting randomised trials becomes challenging. Using real-world data (RWD) to construct control arms for single-arm trials provides an option for comparative data. However, non-randomised treatment comparisons have the potential to be biased and cause concern for decision-makers. Using the example of pralsetinib from a RET fusion-positive aNSCLC single-arm trial (NCT03037385), we demonstrate a relative survival benefit when compared to pembrolizumab monotherapy and pembrolizumab with chemotherapy RWD cohorts. Quantitative bias analyses show that results for the RWD-trial comparisons are robust to data missingness, potential poorer outcomes in RWD and residual confounding. Overall, the study provides evidence in favour of pralsetinib as a first-line treatment for RET fusion-positive aNSCLC. The quantification of potential bias performed in this study can be used as a template for future studies of this nature.
dc.formatElectronic
dc.format.extent3500 -
dc.languageeng
dc.language.isoengen_US
dc.publisherNATURE PORTFOLIOen_US
dc.relation.ispartofNature Communications
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectCarcinoma, Non-Small-Cell Lung
dc.subjectHumans
dc.subjectLung Neoplasms
dc.subjectPyrazoles
dc.subjectPyridines
dc.subjectPyrimidines
dc.titleAddressing challenges with real-world synthetic control arms to demonstrate the comparative effectiveness of Pralsetinib in non-small cell lung cancer.en_US
dc.typeJournal Article
dcterms.dateAccepted2022-05-25
dc.date.updated2022-09-06T13:03:49Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1038/s41467-022-30908-1en_US
rioxxterms.licenseref.startdate2022-06-17
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/35715405
pubs.issue1
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology/Thoracic Oncology (hon.)
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1038/s41467-022-30908-1
pubs.volume13
dc.contributor.icrauthorPopat, Sanjay
icr.provenanceDeposited by Mr Arek Surman on 2022-09-06. Deposit type is initial. No. of files: 1. Files: Addressing challenges with real-world synthetic control arms to demonstrate the comparative effectiveness of Pralsetinib in .pdf


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