Publication: Novel Somay's GLUCAR index efficiently predicts survival outcomes in locally advanced pancreas cancer patients receiving definitive chemoradiotherapy: a propensity-score-matched cohort analysis
dc.contributor.coauthor | Topkan, Erkan | |
dc.contributor.coauthor | Öztürk, Düriye | |
dc.contributor.department | KUH (Koç University Hospital) | |
dc.contributor.department | School of Medicine | |
dc.contributor.kuauthor | Durankuş, Nilüfer Kılıç | |
dc.contributor.kuauthor | Selek, Uğur | |
dc.contributor.kuauthor | Şenyürek, Şükran | |
dc.contributor.schoolcollegeinstitute | KUH (KOÇ UNIVERSITY HOSPITAL) | |
dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
dc.date.accessioned | 2024-12-29T09:38:36Z | |
dc.date.issued | 2024 | |
dc.description.abstract | Background: Propensity score matching (PSM) was used to investigate the prognostic value of a novel GLUCAR index [Glucose x (C-reactive protein divided by albumin)] in unresectable locally advanced pancreatic cancer (LA-NPC) patients who received definitive concurrent chemoradiotherapy (CCRT). Methods: The PSM analysis comprised 142 LA-PAC patients subjected to definitive CCRT. Receiver operating characteristic (ROC) curve analysis was utilized to identify relevant pre-CCRT cutoffs that could effectively stratify survival results. The primary and secondary objectives were the correlations between the pre-CCRT GLUCAR measures and overall survival (OS) and progression-free survival (PFS). Results: The ROC analysis revealed significance at 43.3 for PFS [area under the curve (AUC): 85.1%;sensitivity: 76.8%;specificity: 74.2%;J-index: 0.510)] and 42.8 for OS (AUC: 81.8%;sensitivity: 74.2%;specificity: 71.7%;J-index: 0.459). Given that these cutoff points were close, the standard cutoff point, 42.8, was selected for further analysis. Comparative survival analyses showed that pre-CCRT GLUCAR >= 42.8 (n = 71) measures were associated with significantly shorter median PFS (4.7 vs. 15.8 months;p < 0.001) and OS (10.1 vs. 25.4 months;p < 0.001) durations compared to GLUCAR < 42.8 measures (n = 71). The multivariate analysis results confirmed the independent significance of the GLUCAR index on PFS (p < 0.001) and OS (p < 0.001) outcomes. Conclusions: Elevated pre-CCRT GLUCAR levels are robustly and independently linked to significantly poorer PFS and OS outcomes in unresectable LA-PAC patients treated with definitive CCRT. | |
dc.description.indexedby | WOS | |
dc.description.indexedby | Scopus | |
dc.description.indexedby | PubMed | |
dc.description.issue | 7 | |
dc.description.openaccess | Green Published, gold | |
dc.description.publisherscope | International | |
dc.description.sponsoredbyTubitakEu | N/A | |
dc.description.volume | 14 | |
dc.identifier.doi | 10.3390/jpm14070746 | |
dc.identifier.eissn | 2075-4426 | |
dc.identifier.quartile | Q1 | |
dc.identifier.scopus | 2-s2.0-85199538637 | |
dc.identifier.uri | https://doi.org/10.3390/jpm14070746 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/22747 | |
dc.identifier.wos | 1278445800001 | |
dc.keywords | Pancreatic cancer | |
dc.keywords | Prognosis | |
dc.keywords | Glucose | |
dc.keywords | C-reactive protein-to-albumin ratio | |
dc.keywords | GLUCAR index | |
dc.language.iso | eng | |
dc.publisher | MDPI | |
dc.relation.ispartof | Journal of Personalized Medicine | |
dc.subject | Health care sciences and services | |
dc.subject | Medicine | |
dc.subject | General medicine | |
dc.subject | Internal medicine | |
dc.title | Novel Somay's GLUCAR index efficiently predicts survival outcomes in locally advanced pancreas cancer patients receiving definitive chemoradiotherapy: a propensity-score-matched cohort analysis | |
dc.type | Journal Article | |
dspace.entity.type | Publication | |
local.contributor.kuauthor | Şenyürek, Şükran | |
local.contributor.kuauthor | Durankuş, Nilüfer Kılıç | |
local.contributor.kuauthor | Selek, Uğur | |
local.publication.orgunit1 | SCHOOL OF MEDICINE | |
local.publication.orgunit1 | KUH (KOÇ UNIVERSITY HOSPITAL) | |
local.publication.orgunit2 | KUH (Koç University Hospital) | |
local.publication.orgunit2 | School of Medicine | |
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relation.isOrgUnitOfPublication | d02929e1-2a70-44f0-ae17-7819f587bedd | |
relation.isOrgUnitOfPublication.latestForDiscovery | f91d21f0-6b13-46ce-939a-db68e4c8d2ab | |
relation.isParentOrgUnitOfPublication | 055775c9-9efe-43ec-814f-f6d771fa6dee | |
relation.isParentOrgUnitOfPublication | 17f2dc8e-6e54-4fa8-b5e0-d6415123a93e | |
relation.isParentOrgUnitOfPublication.latestForDiscovery | 055775c9-9efe-43ec-814f-f6d771fa6dee |
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