Low Systemic Inflammation Response Index Predicts Good Prognosis in Locally Advanced Pancreatic Carcinoma Patients Treated with Concurrent Chemoradiotherapy

Author:

Topkan Erkan1ORCID,Mertsoylu Huseyin2ORCID,Kucuk Ahmet3ORCID,Besen Ali Ayberk2ORCID,Sezer Ahmet2,Sezen Duygu4,Bolukbasi Yasemin4,Selek Ugur45ORCID,Pehlivan Berrin6

Affiliation:

1. Department of Radiation Oncology, Baskent University Medical Faculty, Adana, Turkey

2. Department of Medical Oncology, Baskent University Medical Faculty, Adana, Turkey

3. Mersin City Education and Research Hospital, Radiation Oncology Clinics, Mersin, Turkey

4. Department of Radiation Oncology, Koc University School of Medicine, Istanbul, Turkey

5. Department of Radiation Oncology, The University of Texas, MD Anderson Cancer Center, Houston, TX, USA

6. Department of Radiation Oncology, Bahcesehir University, Istanbul/, Turkey

Abstract

Background. We investigated the prognostic significance of pretreatment systemic inflammation response index (SIRI) in locally advanced pancreatic carcinoma (LAPC) patients treated with concurrent chemoradiotherapy (CRT). Methods. Present retrospective cohort analysis investigated consecutive 154 LAPC patients who received radical CRT. The SIRI was defined as: SIRI=neutrophil×monocyte/lymphocytecounts. Ideal SIRI cutoff(s) influencing overall survival (OS) and progression-free survival (PFS) results were sought by using receiver operating characteristic (ROC) curve analysis. The primary endpoint was the interaction between the SIRI and OS results. Results. The median follow-up, PFS, and OS durations were 14.3 (range: 2.9-74.6), 7.9 [%95 confidence interval (CI): 5.7-10.1), and 14.7 months (%95 CI: 11.4-18.0) for the entire cohort, respectively. ROC curve analyses determined the ideal SIRI cutoff that exhibiting a significant link with OS and PFS outcomes at the rounded 1.6 point (AUC: 74.3%; sensitivity: 73.8%; specificity: 70.1%).The SIRI <1.6 patients (N=58) had significantly superior median PFS (13.8 versus 6.7 months; P<0.001) and OS (28.6 versus 12.6 months; P<0.001) lengths than SIRI ≥1.6 patients (N=96), respectively. Although the N0 (versus N1; P<0.05) and CA 19-9 ≤90 U/mL (versus >90 U/mL) appeared as the other significant associates of better OS and PFS in univariate analyses, yet the results of multivariate analyses confirmed the SIRI <1.6 as the independent indicator of superior OS and PFS (P<0.001 for each). Conclusion. Pretreatment SIRI is a novel independent prognosticator that may further enhance the conventional tumor-node-metastases staging system in a more precise prediction of the OS and PFS outcomes of LAPC patients after radical CRT.

Publisher

Hindawi Limited

Subject

Gastroenterology,Hepatology

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