Publication: The prognostic value of the novel global immune-nutrition-inflammation index (gini) in stage iiic non-small cell lung cancer patients treated with concurrent chemoradiotherapy
dc.contributor.coauthor | Topkan, Erkan | |
dc.contributor.coauthor | Pehlivan, Berrin | |
dc.contributor.coauthor | Kucuk, Ahmet | |
dc.contributor.coauthor | Ozturk, Duriye | |
dc.contributor.coauthor | Ozdemir, Beyza Sirin | |
dc.contributor.coauthor | Besen, Ali Ayberk | |
dc.contributor.coauthor | Mertsoylu, Huseyin | |
dc.contributor.department | School of Medicine | |
dc.contributor.kuauthor | Selek, Uğur | |
dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
dc.date.accessioned | 2024-12-29T09:40:24Z | |
dc.date.issued | 2023 | |
dc.description.abstract | Background: We sought to determine the prognostic value of the newly developed Global Immune-Nutrition-Inflammation Index (GINI) in patients with stage IIIC non-small cell lung cancer (NSCLC) who underwent definitive concurrent chemoradiotherapy (CCRT). Methods: This study was conducted on a cohort of 802 newly diagnosed stage IIIC NSCLC patients who underwent CCRT. The novel GINI created first here was defined as follows: GINI = [C-reactive protein × Platelets × Monocytes × Neutrophils] ÷ [Albumin × Lymphocytes]. The receiver operating characteristic (ROC) curve analysis was used to determine the optimal pre-CCRT GINI cut-off value that substantially interacts with the locoregional progression-free (LRPFS), progression-free (PFS), and overall survival (OS). Results: The optimal pre-CCRT GINI cutoff was 1562 (AUC: 76.1%; sensitivity: 72.4%; specificity: 68.2%; Youden index: 0.406). Patients presenting with a GINI ≥ 1562 had substantially shorter median LRPFS (13.3 vs. 18.4 months; p < 0.001), PFS (10.2 vs. 14.3 months; p < 0.001), and OS (19.1 vs. 37.8 months; p < 0.001) durations than those with a GINI < 1562. Results of the multivariate analysis revealed that the pre-CCRT GINI ≥ 1562 (vs. <1562), T4 tumor (vs. T3), and receiving only 1 cycle of concurrent chemotherapy (vs. 2–3 cycles) were the factors independently associated with poorer LRPS (p < 0.05 for each), PFS (p < 0.05 for each), and OS (p < 0.05 for each). Conclusion: The newly developed GINI index efficiently divided the stage IIIC NSCLSC patients into two subgroups with substantially different median and long-term survival outcomes. | |
dc.description.indexedby | WOS | |
dc.description.indexedby | PubMed | |
dc.description.issue | 18 | |
dc.description.openaccess | All Open Access | |
dc.description.openaccess | Gold Open Access | |
dc.description.openaccess | Green Open Access | |
dc.description.publisherscope | International | |
dc.description.sponsoredbyTubitakEu | N/A | |
dc.description.volume | 15 | |
dc.identifier.doi | 10.3390/cancers15184512 | |
dc.identifier.eissn | 2072-6694 | |
dc.identifier.quartile | Q1 | |
dc.identifier.uri | https://doi.org/10.3390/cancers15184512 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/23306 | |
dc.identifier.wos | 1163864300001 | |
dc.keywords | Biological marker | |
dc.keywords | Chemoradiotherapy | |
dc.keywords | Global immune-nutrition-inflammation index | |
dc.keywords | Non-small cell lung cancer | |
dc.keywords | Prognosis | |
dc.keywords | Survival | |
dc.language.iso | eng | |
dc.publisher | Multidisciplinary Digital Publishing Institute (MDPI) | |
dc.relation.ispartof | Cancers | |
dc.subject | Oncology | |
dc.title | The prognostic value of the novel global immune-nutrition-inflammation index (gini) in stage iiic non-small cell lung cancer patients treated with concurrent chemoradiotherapy | |
dc.type | Journal Article | |
dspace.entity.type | Publication | |
local.contributor.kuauthor | Selek, Uğur | |
local.publication.orgunit1 | SCHOOL OF MEDICINE | |
local.publication.orgunit2 | School of Medicine | |
relation.isOrgUnitOfPublication | d02929e1-2a70-44f0-ae17-7819f587bedd | |
relation.isOrgUnitOfPublication.latestForDiscovery | d02929e1-2a70-44f0-ae17-7819f587bedd | |
relation.isParentOrgUnitOfPublication | 17f2dc8e-6e54-4fa8-b5e0-d6415123a93e | |
relation.isParentOrgUnitOfPublication.latestForDiscovery | 17f2dc8e-6e54-4fa8-b5e0-d6415123a93e |
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