dc.contributor.author | Reckamp, KL | |
dc.contributor.author | Lin, HM | |
dc.contributor.author | Cranmer, H | |
dc.contributor.author | Wu, Y | |
dc.contributor.author | Zhang, P | |
dc.contributor.author | Walton, LJ | |
dc.contributor.author | Kay, S | |
dc.contributor.author | Cichewicz, A | |
dc.contributor.author | Neupane, B | |
dc.contributor.author | Fahrbach, K | |
dc.contributor.author | Popat, S | |
dc.contributor.author | Camidge, DR | |
dc.coverage.spatial | England | |
dc.date.accessioned | 2022-08-11T11:12:02Z | |
dc.date.available | 2022-08-11T11:12:02Z | |
dc.date.issued | 2022-05-24 | |
dc.identifier.citation | Future Oncology, 2022, 18 (20), pp. 2499 - 2510 | en_US |
dc.identifier.issn | 1479-6694 | |
dc.identifier.uri | https://repository.icr.ac.uk/handle/internal/5259 | |
dc.identifier.eissn | 1744-8301 | |
dc.identifier.eissn | 1744-8301 | |
dc.identifier.doi | 10.2217/fon-2022-0194 | |
dc.identifier.doi | 10.2217/fon-2022-0194 | |
dc.description.abstract | Aim: To conduct an indirect treatment comparison (ITC) of the relative efficacy of brigatinib and alectinib for progression-free survival in people with tyrosine kinase inhibitor (TKI)-naive ALK-positive non-small-cell lung cancer (NSCLC). Methods: Final aggregate and patient-level data from the ALTA-1L trial comparing brigatinib to crizotinib and published aggregate data from ALEX (comparing alectinib to crizotinib) were contrasted using Bucher ITC and matching-adjusted indirect comparisons (MAICs). Results: No statistically significant differences were identified between brigatinib and alectinib in reducing the risk of disease progression overall and in patients with baseline central nervous system metastases. Conclusion: Brigatinib appeared similar to alectinib in reducing risk of disease progression for people with TKI-naive ALK-positive NSCLC. | |
dc.format | Print-Electronic | |
dc.format.extent | 2499 - 2510 | |
dc.language | eng | |
dc.language.iso | eng | en_US |
dc.publisher | FUTURE MEDICINE LTD | en_US |
dc.relation.ispartof | Future Oncology | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ | en_US |
dc.subject | ALK inhibitor | |
dc.subject | Bucher ITC | |
dc.subject | NSCLC | |
dc.subject | alectinib | |
dc.subject | brigatinib | |
dc.subject | matching-adjusted indirect comparison | |
dc.subject | progression-free survival | |
dc.subject | systematic literature review | |
dc.subject | Anaplastic Lymphoma Kinase | |
dc.subject | Carbazoles | |
dc.subject | Carcinoma, Non-Small-Cell Lung | |
dc.subject | Clinical Trials as Topic | |
dc.subject | Crizotinib | |
dc.subject | Disease Progression | |
dc.subject | Humans | |
dc.subject | Lung Neoplasms | |
dc.subject | Organophosphorus Compounds | |
dc.subject | Piperidines | |
dc.subject | Protein Kinase Inhibitors | |
dc.subject | Pyrimidines | |
dc.title | Indirect comparisons of brigatinib and alectinib for front-line ALK-positive non-small-cell lung cancer. | en_US |
dc.type | Journal Article | |
dcterms.dateAccepted | 2022-04-27 | |
dc.date.updated | 2022-08-11T11:10:59Z | |
rioxxterms.version | VoR | en_US |
rioxxterms.versionofrecord | 10.2217/fon-2022-0194 | en_US |
rioxxterms.licenseref.startdate | 2022-05-24 | |
rioxxterms.type | Journal Article/Review | en_US |
pubs.author-url | https://www.ncbi.nlm.nih.gov/pubmed/35608148 | |
pubs.issue | 20 | |
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-status | Published | |
pubs.volume | 18 | |
dc.contributor.icrauthor | Popat, Sanjay | |
icr.provenance | Deposited by Mr Arek Surman on 2022-08-11. Deposit type is initial. No. of files: 1. Files: fon-2022-0194.pdf | |