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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
DC Field | Value | Language |
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dc.contributor.author | Tan, Daniel S.W. | - |
dc.contributor.author | Kim, Sang-We | - |
dc.contributor.author | Ponce Aix, Santiago | - |
dc.contributor.author | Sequist, Lecia V. | - |
dc.contributor.author | Smit, Egbert F. | - |
dc.contributor.author | Yang, James C.H. | - |
dc.contributor.author | Hida, Toyoaki | - |
dc.contributor.author | Toyozawa, Ryo | - |
dc.contributor.author | Felip, Enriqueta | - |
dc.contributor.author | Wolf, Juergen | - |
dc.contributor.author | Grohé, Christian | - |
dc.contributor.author | Leighl, Natasha B. | - |
dc.contributor.author | Riely, Gregory | - |
dc.contributor.author | Cui, Xiaoming | - |
dc.contributor.author | Zou, Mike | - |
dc.contributor.author | Ghebremariam, Samson | - |
dc.contributor.author | O'Sullivan-Djentuh, Leslie | - |
dc.contributor.author | Belli, Riccardo | - |
dc.contributor.author | Giovannini, Monica | - |
dc.contributor.author | Kim, Dong-Wan | - |
dc.date.accessioned | 2022-09-29T03:19:08Z | - |
dc.date.available | 2022-09-29T03:19:08Z | - |
dc.date.created | 2022-07-28 | - |
dc.date.created | 2022-07-28 | - |
dc.date.created | 2022-07-28 | - |
dc.date.created | 2022-07-28 | - |
dc.date.created | 2022-07-28 | - |
dc.date.created | 2022-07-28 | - |
dc.date.created | 2022-07-28 | - |
dc.date.created | 2022-07-28 | - |
dc.date.created | 2022-07-28 | - |
dc.date.issued | 2022-09 | - |
dc.identifier.citation | European Journal of Cancer, Vol.172, pp.276-286 | - |
dc.identifier.issn | 0959-8049 | - |
dc.identifier.uri | https://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.language | 영어 | - |
dc.publisher | Pergamon Press Ltd. | - |
dc.title | Nazartinib for treatment-naive EGFR-mutant non−small cell lung cancer: Results of a phase 2, single-arm, open-label study | - |
dc.title.alternative | Nazartinib for treatment-naive EGFR-mutant non-small cell lung cancer: Results of a phase 2, single-arm, open-label study | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.ejca.2022.05.023 | - |
dc.citation.journaltitle | European Journal of Cancer | - |
dc.identifier.wosid | 000829363200003 | - |
dc.identifier.scopusid | 2-s2.0-85133930125 | - |
dc.citation.endpage | 286 | - |
dc.citation.startpage | 276 | - |
dc.citation.volume | 172 | - |
dc.description.isOpenAccess | Y | - |
dc.contributor.affiliatedAuthor | Kim, Dong-Wan | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.subject.keywordPlus | BRAIN METASTASES | - |
dc.subject.keywordPlus | RESISTANCE | - |
dc.subject.keywordPlus | OSIMERTINIB | - |
dc.subject.keywordPlus | MUTATIONS | - |
dc.subject.keywordPlus | FAILURE | - |
dc.subject.keywordPlus | CHEMOTHERAPY | - |
dc.subject.keywordPlus | INHIBITORS | - |
dc.subject.keywordPlus | GEFITINIB | - |
dc.subject.keywordPlus | EGF816 | - |
dc.subject.keywordPlus | TKI | - |
dc.subject.keywordAuthor | EGFR | - |
dc.subject.keywordAuthor | Nazartinib | - |
dc.subject.keywordAuthor | NSCLC | - |
dc.subject.keywordAuthor | Third-generation EGFR-TKI | - |
dc.subject.keywordAuthor | Treatment-naive | - |
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