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Nazartinib for treatment-naive EGFR-mutant non−small cell lung cancer: Results of a phase 2, single-arm, open-label study : Nazartinib for treatment-naive EGFR-mutant non-small cell lung cancer: Results of a phase 2, single-arm, open-label study

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dc.contributor.authorTan, Daniel S.W.-
dc.contributor.authorKim, Sang-We-
dc.contributor.authorPonce Aix, Santiago-
dc.contributor.authorSequist, Lecia V.-
dc.contributor.authorSmit, Egbert F.-
dc.contributor.authorYang, James C.H.-
dc.contributor.authorHida, Toyoaki-
dc.contributor.authorToyozawa, Ryo-
dc.contributor.authorFelip, Enriqueta-
dc.contributor.authorWolf, Juergen-
dc.contributor.authorGrohé, Christian-
dc.contributor.authorLeighl, Natasha B.-
dc.contributor.authorRiely, Gregory-
dc.contributor.authorCui, Xiaoming-
dc.contributor.authorZou, Mike-
dc.contributor.authorGhebremariam, Samson-
dc.contributor.authorO'Sullivan-Djentuh, Leslie-
dc.contributor.authorBelli, Riccardo-
dc.contributor.authorGiovannini, Monica-
dc.contributor.authorKim, Dong-Wan-
dc.date.accessioned2022-09-29T03:19:08Z-
dc.date.available2022-09-29T03:19:08Z-
dc.date.created2022-07-28-
dc.date.created2022-07-28-
dc.date.created2022-07-28-
dc.date.created2022-07-28-
dc.date.created2022-07-28-
dc.date.created2022-07-28-
dc.date.created2022-07-28-
dc.date.created2022-07-28-
dc.date.issued2022-09-
dc.identifier.citationEuropean Journal of Cancer, Vol.172, pp.276-286-
dc.identifier.issn0959-8049-
dc.identifier.urihttps://hdl.handle.net/10371/184697-
dc.description.abstract© 2022Introduction: Nazartinib, a novel third-generation EGFR-tyrosine kinase inhibitor, previously demonstrated antitumor activity and manageable safety in patients with EGFR-mutant advanced non−small cell lung cancer (NSCLC) who received ≤ 3 prior lines of systemic therapy. Herein, we report phase 2 efficacy and safety of first-line nazartinib. Methods: This single-arm, open-label, global study enrolled treatment-naive adult patients with stage IIIB/IV NSCLC harboring EGFR-activating mutations (eg, L858R and/or ex19del). Patients with neurologically stable and controlled brain metastases were also eligible. Patients received oral nazartinib 150 mg once daily. The primary endpoint was Blinded Independent Review Committee (BIRC)-assessed overall response rate (ORR) per RECIST v1.1. Results: Forty-five patients received ≥ 1 dose of nazartinib. The median follow-up time from enrollment to data cutoff (November 1, 2019) was 30 months (range: 25–34). The BIRC-assessed ORR was 69% (95% CI, 53–82). The median progression-free survival (PFS) was 18 months (95% CI, 15-not estimable [NE]). The median overall survival was NE. In patients with baseline brain metastases (n = 18), the ORR and median PFS (95% CIs) were 67% (41–87) and 17 months (11–21). Seventeen of 18 patients had brain metastases as non-target lesions; the CNS lesions were absent/normalized in 9 of 17 (53%). Only 2 of 27 patients without baseline brain metastases developed new brain metastases postbaseline. Most frequent adverse events (≥ 25%, any grade, all-causality) were diarrhea (47%), maculopapular rash (38%), pyrexia (29%), cough, and stomatitis (27% each). Conclusions: First-line nazartinib demonstrated promising efficacy, including clinically meaningful antitumor activity in the brain, and manageable safety in patients with EGFR-mutant NSCLC. Trial registration: ClinicalTrials.gov https://clinicaltrials.gov/ct2/show/NCT02108964.-
dc.language영어-
dc.publisherPergamon Press Ltd.-
dc.titleNazartinib for treatment-naive EGFR-mutant non−small cell lung cancer: Results of a phase 2, single-arm, open-label study-
dc.title.alternativeNazartinib for treatment-naive EGFR-mutant non-small cell lung cancer: Results of a phase 2, single-arm, open-label study-
dc.typeArticle-
dc.identifier.doi10.1016/j.ejca.2022.05.023-
dc.citation.journaltitleEuropean Journal of Cancer-
dc.identifier.wosid000829363200003-
dc.identifier.scopusid2-s2.0-85133930125-
dc.citation.endpage286-
dc.citation.startpage276-
dc.citation.volume172-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorKim, Dong-Wan-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusBRAIN METASTASES-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusOSIMERTINIB-
dc.subject.keywordPlusMUTATIONS-
dc.subject.keywordPlusFAILURE-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.subject.keywordPlusINHIBITORS-
dc.subject.keywordPlusGEFITINIB-
dc.subject.keywordPlusEGF816-
dc.subject.keywordPlusTKI-
dc.subject.keywordAuthorEGFR-
dc.subject.keywordAuthorNazartinib-
dc.subject.keywordAuthorNSCLC-
dc.subject.keywordAuthorThird-generation EGFR-TKI-
dc.subject.keywordAuthorTreatment-naive-
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