Cited 27 times in
Nivolumab in advanced non-small-cell lung cancer patients who failed prior platinum-based chemotherapy
DC Field | Value | Language |
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dc.contributor.author | 김주항 | - |
dc.contributor.author | 조병철 | - |
dc.date.accessioned | 2022-08-16T01:33:32Z | - |
dc.date.available | 2022-08-16T01:33:32Z | - |
dc.date.issued | 2018-08 | - |
dc.identifier.issn | 0169-5002 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/188944 | - |
dc.description.abstract | Objectives: 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.description.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | Elsevier Scientific Publishers | - |
dc.relation.isPartOf | LUNG CANCER | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Aged, 80 and over | - |
dc.subject.MESH | Antineoplastic Agents / therapeutic use* | - |
dc.subject.MESH | Carcinoma, Non-Small-Cell Lung / drug therapy* | - |
dc.subject.MESH | Carcinoma, Non-Small-Cell Lung / epidemiology | - |
dc.subject.MESH | Carcinoma, Non-Small-Cell Lung / mortality | - |
dc.subject.MESH | Drug Resistance, Neoplasm | - |
dc.subject.MESH | Drug-Related Side Effects and Adverse Reactions / epidemiology* | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Follow-Up Studies | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Korea / epidemiology | - |
dc.subject.MESH | Lung Neoplasms / drug therapy* | - |
dc.subject.MESH | Lung Neoplasms / epidemiology | - |
dc.subject.MESH | Lung Neoplasms / mortality | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Neoplasm Recurrence, Local | - |
dc.subject.MESH | Neoplasm Staging | - |
dc.subject.MESH | Nivolumab / therapeutic use* | - |
dc.subject.MESH | Platinum Compounds / therapeutic use | - |
dc.subject.MESH | Pneumonia / epidemiology* | - |
dc.subject.MESH | Pneumonia / etiology | - |
dc.subject.MESH | Prospective Studies | - |
dc.subject.MESH | Survival Analysis | - |
dc.title | Nivolumab in advanced non-small-cell lung cancer patients who failed prior platinum-based chemotherapy | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
dc.contributor.googleauthor | Jong Seok Lee | - |
dc.contributor.googleauthor | Ki Hyeong Lee | - |
dc.contributor.googleauthor | Eun Kyung Cho | - |
dc.contributor.googleauthor | Dong-Wan Kim | - |
dc.contributor.googleauthor | Sang-We Kim | - |
dc.contributor.googleauthor | Joo-Hang Kim | - |
dc.contributor.googleauthor | Byoung Chul Cho | - |
dc.contributor.googleauthor | Jin Hyoung Kang | - |
dc.contributor.googleauthor | Ji-Youn Han | - |
dc.contributor.googleauthor | Young Joo Min | - |
dc.contributor.googleauthor | Keunchil Park | - |
dc.identifier.doi | 10.1016/j.lungcan.2018.05.023 | - |
dc.contributor.localId | A00945 | - |
dc.contributor.localId | A03822 | - |
dc.relation.journalcode | J02174 | - |
dc.identifier.eissn | 1872-8332 | - |
dc.identifier.pmid | 30032838 | - |
dc.subject.keyword | Nivolumab | - |
dc.subject.keyword | Non-small cell lung cancer | - |
dc.subject.keyword | Programmed cell death-1 | - |
dc.contributor.alternativeName | Kim, Joo Hang | - |
dc.contributor.affiliatedAuthor | 김주항 | - |
dc.contributor.affiliatedAuthor | 조병철 | - |
dc.citation.volume | 122 | - |
dc.citation.startPage | 234 | - |
dc.citation.endPage | 242 | - |
dc.identifier.bibliographicCitation | LUNG CANCER, Vol.122 : 234-242, 2018-08 | - |
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