The Prognostic Significance of Novel Pancreas Cancer Prognostic Index in Unresectable Locally Advanced Pancreas Cancers Treated with Definitive Concurrent Chemoradiotherapy

dc.contributor.authorTopkan, Erkan
dc.contributor.authorSelek, Ugur
dc.contributor.authorPehlivan, Berrin
dc.contributor.authorKucuk, Ahmet
dc.contributor.authorHaksoyler, Veysel
dc.contributor.authorDurankus, Nulifer Kilic
dc.contributor.authorSezen, Duygu
dc.contributor.authorBolukbasi, Yasemin
dc.contributor.orcID0000-0001-8087-3140en_US
dc.contributor.orcID0000-0001-8120-7123en_US
dc.contributor.orcID0000-0002-4505-2280en_US
dc.contributor.pubmedID34511977en_US
dc.contributor.researcherIDO-5474-2014en_US
dc.contributor.researcherIDAAG-2213-2021en_US
dc.date.accessioned2022-08-23T07:47:40Z
dc.date.available2022-08-23T07:47:40Z
dc.date.issued2021
dc.description.abstractPurpose: We evaluated the prognostic quality of the novel pancreas cancer prognostic index (PCPI), a combination of CA 19-9 and systemic inflammation response index (SIRI), on the outcomes of locally advanced pancreas adenocarcinoma (LAPAC) patients who received concurrent chemoradiotherapy (C-CRT). Methods: This retrospective analysis covered 152 unresectable LAPAC patients treated from 2007 to 2019. Receiver operating characteristic (ROC) curve analysis was used to define ideal cutoff thresholds for the pretreatment CA 19-9 and SIRI measurements, indivi-dually. The associations between the PCPI groups and progression -free-(PFS) and overall survival (OS) comprised the respective primary and secondary endpoints. Results: The ROC curve analysis distinguished the respective rounded optimal cutoffs at 91 U/m/ L (< versus >= 90) and 1.8 (< versus >= 1.8) for CA 19-9 and SIRI, arranging the study cohort into two significantly different survival groups for each, with resultant four likely groups: Group-1: CA 19-9<90 U/m/L and SIRI<1.8, Group-2: CA 19-9<90 U/m/L but SIRI >= 1.8, Group-3: CA 19-9 >= 90 U/ m/L but SIRI<1.8, and Group-4: CA 19-9 >= 90 U/m/L and SIRI >= 1.8. Since the PFS (P=0.79) and OS (P=0.86) estimates of the groups 2 and 3 were statistically indistinct, we merged them as one group and created the novel three-tiered PCPI: PCPI-1: CA 19-9<90 U/m/L and SIRI<1.8, PCPI-2: CA 19-9<90 U/m/L but SIRI >= 1.8 or CA 19-9 >= 90 U/m/L but SIRI<1.8, and PCPI-3: CA 19-9 >= 90 U/m/L and SIRI >= 1.8, respectively. Comparative analyses unveiled that the PCPI-1 and PCPI-3 groups had the respective best and worst PFS (17.0 versus 7.5 versus 4.4 months; P<0.001) and OS (26.1 versus 15.1 versus 7.4 months; P<0.001) outcomes, while the PCPI-2 group posed in between. The multivariate analysis outcomes confirmed the novel three tired PCPI's independent prognostic significance on either of the PFS [HR: 5.38 (95% confidence interval (CI): 4.96-5.80); P<0.001)] and OS [HR: 5.67 (95% CI: 5.19-6.15); P<0.001] endpoints, separately. Conclusion: The new PCPI introduced here can be used as an independent and reliable prog-nostic indicator to divide LAPAC patients into three subgroups with discrete survival results.en_US
dc.identifier.eissn1178-7031en_US
dc.identifier.endpage4444en_US
dc.identifier.scopus2-s2.0-85115027820en_US
dc.identifier.startpage4433en_US
dc.identifier.urihttps://www.dovepress.com/the-prognostic-significance-of-novel-pancreas-cancer-prognostic-index--peer-reviewed-fulltext-article-JIR
dc.identifier.urihttp://hdl.handle.net/11727/7386
dc.identifier.volume14en_US
dc.identifier.wos000692999300001en_US
dc.language.isoengen_US
dc.relation.isversionof10.2147/JIR.S329611en_US
dc.relation.journalJOURNAL OF INFLAMMATION RESEARCHen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectlocally advanced pancreas canceren_US
dc.subjectconcurrent chemoradiotherapyen_US
dc.subjectprognosisen_US
dc.subjectsurvival outcomesen_US
dc.subjectpancreas cancer prognostic indexen_US
dc.titleThe Prognostic Significance of Novel Pancreas Cancer Prognostic Index in Unresectable Locally Advanced Pancreas Cancers Treated with Definitive Concurrent Chemoradiotherapyen_US
dc.typearticleen_US

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