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Licensed Unlicensed Requires Authentication Published by De Gruyter March 24, 2016

Dynamic change of the systemic immune inflammation index predicts the prognosis of patients with hepatocellular carcinoma after curative resection

  • Bei-li Wang , Lu Tian , Xing-Hui Gao , Xiao-Lu Ma , Jiong Wu , Chun-Yan Zhang , Yan Zhou , Wei Guo EMAIL logo and Xin-Rong Yang EMAIL logo

Abstract

Background:

The aim of the study was to determine the utility of the dynamic change and serial monitoring of the systemic immune inflammation index (SII), which was based on the numbers of patients’ lymphocytes (L), platelets (P), neutrophils (N) and defined as P*N/L, for predicting prognosis of patients with hepatocellular carcinoma (HCC) after curative resection.

Methods:

We conducted a prospective study of 163 patients with HCC who underwent curative resection at Zhongshan Hospital from January 2012 to May 2013. SII was calculated using data acquired before and approximately 1 month after surgery. An optimal cutoff value stratified patients into groups with high or low SII. Patients were classified into unfavorable and favorable groups using the dynamic change of the SII. Two groups that were further divided into four categories within the entire cohort and the low-risk subgroups were serially monitored for ≥6 months. Prognostic values of the SII and other factors were determined using the Kaplan-Meier method, the Cox proportional hazards model, and the receiver operating characteristics (ROC) curve.

Results:

The favorable group was likely to have cirrhosis, and the unfavorable group was likely to have larger tumors and a higher recurrence rate. Multivariate analysis revealed that tumor size and dynamic change of the SII were independent risk factors for early recurrence. Moreover, the predictive value of the SII was retained in α-fetoprotein (AFP)-negative and HBeAg-negative-HBV-DNA <2000 IU/mL subgroups. Further, the serial changes of the SII for recurrence and no recurrence groups were statistically significant.

Conclusions:

The dynamic change and serial monitoring of the SII represent new indicators for predicting the early recurrence of HCC determining advance optimal therapy in advance.


Corresponding authors: Wei Guo, PhD, Department of Laboratory Medicine, Zhongshan Hospital, Fudan University, 136 Yi Xue Yuan Road, Shanghai 200032, P.R China, Phone/Fax: +86-21-64041990-2376, E-mail: ; and Xin-Rong Yang, MD, PhD, Liver Cancer Institute, Department of Liver Surgery, Zhongshan Hospital, Fudan University, 136 Yi Xue Yuan Road, Shanghai 200032, P.R China, Phone/Fax: +86-21-64041990-2376, E-mail:
aBei-li Wang and Lu Tian contributed equally to this work.
  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: This study was supported by grants from the National High Technology Research and Development Program (863 Program) of China (2015AA020401), National Key Sci-Tech Project (2013ZX10002010-003 and 2013ZX10002011-004), the National Natural Science Foundation of China (81572064, 81530077, 81472676 and 81372317), the Projects from the Shanghai Science and Technology Commission (14DZ1940300, 14DZ1940302, 14411970200, 134119a1201 and 14140902301), Specialized Research Fund for the Doctoral Program of Higher Education and Research Grants Council Earmarked Research Grants Joint Research Scheme (20130071140008) and the National Science & Technology Pillar Program during the 12th 5-year Plan Period (2012BAI37B01).

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Supplemental Material:

The online version of this article (DOI: 10.1515/cclm-2015-1191) offers supplementary material, available to authorized users.


Received: 2015-12-1
Accepted: 2016-2-15
Published Online: 2016-3-24
Published in Print: 2016-12-1

©2016 Walter de Gruyter GmbH, Berlin/Boston

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