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Nivolumab in advanced non-small-cell lung cancer patients who failed prior platinum-based chemotherapy

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dc.contributor.authorLee, Jong Seok-
dc.contributor.authorLee, Ki Hyeong-
dc.contributor.authorCho, Eun Kyung-
dc.contributor.authorKim, Dong-Wan-
dc.contributor.authorKim, Sang-We-
dc.contributor.authorKim, Joo-Hang-
dc.contributor.authorCho, Byoung Chul-
dc.contributor.authorKang, Jin Hyoung-
dc.contributor.authorHan, Ji-Youn-
dc.contributor.authorMin, Young Joo-
dc.contributor.authorPark, Keunchil-
dc.date.accessioned2020-04-27T11:03:44Z-
dc.date.available2020-04-27T11:03:44Z-
dc.date.created2019-06-26-
dc.date.issued2018-08-
dc.identifier.citationLung Cancer, Vol.122, pp.234-242-
dc.identifier.issn0169-5002-
dc.identifier.other76823-
dc.identifier.urihttps://hdl.handle.net/10371/165235-
dc.description.abstractObjectives: To investigate the efficacy and safety of nivolumab in Korean patients with stage IIIB/IV or recurrent non-small-cell lung cancer (NSCLC) who failed platinum-based chemotherapy. Materials and methods: In this multicenter, open-label, Phase II study, 100 patients with stage IIIB or IV squamous (n = 44) or non-squamous (n = 56) NSCLC received nivolumab 3 mg/kg every 2 weeks for 6 weeks per treatment cycle. Patients continued treatment until disease progression or intolerable adverse events (AEs), and then entered a follow-up phase. The primary efficacy endpoint was the centrally assessed objective response rate (ORR). Results: The ORR was 20.0% (95% confidence interval [CI]: 13.3-28.9%) in the total population, 15.9% (7/44 patients; 95% CI: 7.9-29.4%) in patients with squamous NSCLC, and 23.2% (13/56 patients; 95% CI: 14.1-35.8%) in patients with non-squamous NSCLC. Median overall survival was 13.9 (95% CI: 10.8-18.5) months in the total population, 12.3 (95% CI: 8.2-18.5) months in squamous NSCLC, and 16.3 (95% CI: 10.8,) months in non-squamous NSCLC. Median progression-free survival was 2.8 (95% CI: 1.4-5.7), 2.6 (95% CI: 1.3-5.7), and 5.3 (95% CI: 1.4-7.1) months in the total, squamous, and non-squamous NSCLC populations, respectively. The median duration of response was 11.7 (95% CI: 5.6,), 12.0 (95% CI: 4.8,-), and 12.1 (95% CI: 3.0,-) months in the total, squamous, and non-squamous NSCLC populations, respectively. The most frequent AEs were decreased appetite, dyspnea, and cough in 43 (43.0%), 32 (32.0%), and 29 (29.0%) patients, respectively. The most common Grade >= 3 AE was pneumonia, occurring in 7.0% of patients. Common treatment -related AEs included decreased appetite (14.0%) and pruritus (6.0%), neither of which was Grade >= 3. Conclusion: The efficacy and safety of nivolumab in Korean patients with advanced or recurrent squamous or non-squamous NSCLC are consistent with previous reports.-
dc.language영어-
dc.publisherElsevier BV-
dc.titleNivolumab in advanced non-small-cell lung cancer patients who failed prior platinum-based chemotherapy-
dc.typeArticle-
dc.contributor.AlternativeAuthor김동완-
dc.contributor.AlternativeAuthor이종석-
dc.identifier.doi10.1016/j.lungcan.2018.05.023-
dc.citation.journaltitleLung Cancer-
dc.identifier.wosid000440769900038-
dc.identifier.scopusid2-s2.0-85049013316-
dc.citation.endpage242-
dc.citation.startpage234-
dc.citation.volume122-
dc.identifier.sci000440769900038-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorLee, Jong Seok-
dc.contributor.affiliatedAuthorKim, Dong-Wan-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusRANDOMIZED CONTROLLED-TRIAL-
dc.subject.keywordPlusANTI-PD-1 ANTIBODY-
dc.subject.keywordPlusSOLID TUMORS-
dc.subject.keywordPlus2ND-LINE TREATMENT-
dc.subject.keywordPlusPHASE-III-
dc.subject.keywordPlusDOCETAXEL-
dc.subject.keywordPlusSAFETY-
dc.subject.keywordPlusBMS-936558-
dc.subject.keywordPlusCARCINOMA-
dc.subject.keywordAuthorNivolumab-
dc.subject.keywordAuthorNon-small cell lung cancer-
dc.subject.keywordAuthorProgrammed cell death-1-
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