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dc.contributor.authorAhn, MJ
dc.contributor.authorKim, HR
dc.contributor.authorYang, JCH
dc.contributor.authorHan, J-Y
dc.contributor.authorLi, JY-C
dc.contributor.authorHochmair, MJ
dc.contributor.authorChang, G-C
dc.contributor.authorDelmonte, A
dc.contributor.authorLee, KH
dc.contributor.authorCampelo, RG
dc.contributor.authorGridelli, C
dc.contributor.authorSpira, AI
dc.contributor.authorCalifano, R
dc.contributor.authorGriesinger, F
dc.contributor.authorGhosh, S
dc.contributor.authorFelip, E
dc.contributor.authorKim, D-W
dc.contributor.authorLiu, Y
dc.contributor.authorZhang, P
dc.contributor.authorPopat, S
dc.contributor.authorCamidge, DR
dc.coverage.spatialUnited States
dc.date.accessioned2022-10-05T13:49:12Z
dc.date.available2022-10-05T13:49:12Z
dc.date.issued2022-07-21
dc.identifierS1525-7304(22)00152-8
dc.identifier.citationClinical Lung Cancer, 2022, pp. S1525-7304(22)00152-8 -en_US
dc.identifier.issn1525-7304
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5525
dc.identifier.eissn1938-0690
dc.identifier.eissn1938-0690
dc.identifier.doi10.1016/j.cllc.2022.07.008
dc.description.abstractBACKGROUND: Brigatinib is a next-generation anaplastic lymphoma kinase (ALK) inhibitor with demonstrated efficacy in locally advanced and metastatic non-small cell lung cancer (NSCLC) in crizotinib-refractory and ALK inhibitor-naive settings. This analysis assessed brigatinib in Asian vs. non-Asian patients from the first-line ALTA-1L trial. PATIENTS AND METHODS: This was a subgroup analysis from the phase III ALTA-1L trial of brigatinib vs. crizotinib in ALK inhibitor-naive ALK+ NSCLC. The primary endpoint was progression-free survival (PFS) as assessed by blinded independent review committee (BIRC). Secondary endpoints included confirmed objective response rate (ORR) and overall survival (OS) in the overall population and BIRC-assessed intracranial ORR and PFS in patients with brain metastases. RESULTS: Of the 275 randomized patients, 108 were Asian. Brigatinib showed consistent superiority in BIRC-assessed PFS vs. crizotinib in Asian (hazard ratio [HR]: 0.35 [95% CI: 0.20-0.59]; log-rank P = .0001; median 24.0 vs. 11.1 months) and non-Asian (HR: 0.56 [95% CI: 0.38-0.84]; log-rank P = .0041; median 24.7 vs. 9.4 months) patients. Results were consistent with investigator-assessed PFS and BIRC-assessed intracranial PFS. Brigatinib was well tolerated. Toxicity profiles and dose modification rates were similar between Asian and non-Asian patients. CONCLUSION: Efficacy with brigatinib was consistently better than with crizotinib in Asian and non-Asian patients with locally advanced or metastatic ALK inhibitor-naive ALK-+ NSCLC. There were no clinically notable differences in overall safety in Asian vs. non-Asian patients.
dc.formatPrint-Electronic
dc.format.extentS1525-7304(22)00152-8 -
dc.languageeng
dc.language.isoengen_US
dc.publisherElsevier BVen_US
dc.relation.ispartofClinical Lung Cancer
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectALK TKI-naive
dc.subjectAnaplastic lymphoma kinase
dc.subjectClinical trial
dc.subjectFirst line
dc.subjectTyrosine kinase inhibitor
dc.titleEfficacy and Safety of Brigatinib Compared With Crizotinib in Asian vs. Non-Asian Patients With Locally Advanced or Metastatic ALK-Inhibitor-Naive ALK+ Non-Small Cell Lung Cancer: Final Results From the Phase III ALTA-1L Study.en_US
dc.typeJournal Article
dcterms.dateAccepted2022-07-16
dc.date.updated2022-10-05T13:48:34Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1016/j.cllc.2022.07.008en_US
rioxxterms.licenseref.startdate2022-07-21
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/36038416
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/10.1016/j.cllc.2022.07.008
dc.contributor.icrauthorPopat, Sanjay
icr.provenanceDeposited by Mr Arek Surman on 2022-10-05. Deposit type is initial. No. of files: 1. Files: 1-s2.0-S1525730422001528-main.pdf


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