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Geriatric Nutritional Risk Index as a prognostic marker in patients with extensive-stage disease small cell lung cancer: Results from a randomized controlled trial

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dc.contributor.authorLee, Gyeong-Won-
dc.contributor.authorGo, Se-Il-
dc.contributor.authorKim, Dong-Wan-
dc.contributor.authorKim, Hoon-Gu-
dc.contributor.authorKim, Joo-Hang-
dc.contributor.authorAn, Ho Jung-
dc.contributor.authorJang, Joung Soon-
dc.contributor.authorKim, Bong-Seog-
dc.contributor.authorHahn, Seokyung-
dc.contributor.authorHeo, Dae Seog-
dc.date.accessioned2022-12-26T13:16:20Z-
dc.date.available2022-12-26T13:16:20Z-
dc.date.issued2020-01-
dc.identifier.issn1759-7706-
dc.identifier.issn1759-7714-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/7092-
dc.description.abstractBackground Clinical impact of the Geriatric Nutritional Risk Index (GNRI) in patients with extensive-stage disease small cell lung cancer (ED-SCLC) have not previously been reported. Methods This study analyzed 352 patients enrolled in a previous randomized phase III trial comparing the efficacy of irinotecan plus cisplatin with that of etoposide plus cisplatin as the first-line therapy for ED-SCLC. GNRI values were calculated using serum albumin levels and actual and ideal bodyweights. Patients with a GNRI > 98, 92-98, and <92 were grouped into no, low, and moderate/major risk groups, respectively. Results The objective response rates were 63.2%, 52.6%, and 49.2% in the no, low, and moderate/major risk groups, respectively (P = 0.024). The median progression-free survival (PFS) was shorter in patients with a lower GNRI than in those with a higher GNRI (no vs. low vs. moderate/major risk group; 6.5 vs. 5.8 vs. 5.9 months, respectively; P = 0.028). There were significant differences in median overall survival (OS) according to GNRI (no vs. low vs. moderate/major risk group; 13.2 vs. 10.3 vs. 8.4 months, respectively; P < 0.001). Multivariate analysis revealed that being in the moderate/major risk group was an independent poor prognostic factor for PFS (hazard ratio [HR]: 1.300, 95% confidence interval [CI]: 1.012-1.670; P = 0.040) and OS (HR: 1.539; 95% CI: 1.069-2.216; P = 0.020). Conclusions This prospective study shows that a low GNRI value was associated with a poor prognosis, and it supports the relationship between systemic inflammation, nutritional status, and clinical outcomes in patients with ED-SCLC.Key points Significant findings of the study The lower GNRI group had a low response rate to chemotherapy for ED-SCLC. The HRs for PFS and OS were 1.300 and 1.539 in the patients with GNRI < 92. What this study adds Low GNRI is associated with poor prognosis in ED-SCLC.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherWILEY-
dc.titleGeriatric Nutritional Risk Index as a prognostic marker in patients with extensive-stage disease small cell lung cancer: Results from a randomized controlled trial-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1111/1759-7714.13229-
dc.identifier.scopusid2-s2.0-85074846303-
dc.identifier.wosid000505275100010-
dc.identifier.bibliographicCitationTHORACIC CANCER, v.11, no.1, pp 62 - 71-
dc.citation.titleTHORACIC CANCER-
dc.citation.volume11-
dc.citation.number1-
dc.citation.startPage62-
dc.citation.endPage71-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaRespiratory System-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryRespiratory System-
dc.subject.keywordPlusPHASE-III TRIAL-
dc.subject.keywordPlus1ST-LINE TREATMENT-
dc.subject.keywordPlusVASCULAR-PERMEABILITY-
dc.subject.keywordPlusCISPLATIN-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordPlusALBUMIN-
dc.subject.keywordPlusINFLAMMATION-
dc.subject.keywordPlusETOPOSIDE-
dc.subject.keywordPlusIRINOTECAN-
dc.subject.keywordPlusCACHEXIA-
dc.subject.keywordAuthorCachexia-
dc.subject.keywordAuthorinflammation-
dc.subject.keywordAuthornutrition assessment-
dc.subject.keywordAuthorsmall cell lung carcinoma-
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