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Authors Chen Z, Wang K, Lu H, Xue D, Fan M, Zhuang Q, Yin S, He X, Xu R
Received 9 September 2018
Accepted for publication 28 November 2018
Published 18 January 2019 Volume 2019:11 Pages 909—919
DOI https://doi.org/10.2147/CMAR.S186976
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Amy Norman
Peer reviewer comments 2
Editor who approved publication: Dr Chien-Feng Li
Purpose: In the
present study, we aimed to evaluate the prognostic significance of the systemic
inflammation response index (SIRI), which was defined based on peripheral blood
counts of neutrophils, lymphocytes, and monocytes, in patients with localized
or locally advanced clear cell renal cell carcinoma (CCRCC).
Patients and methods: The
prognostic value of SIRI was evaluated in a primary cohort consisting of 414
patients with localized or locally advanced CCRCC and then further validated in
an independent cohort composed of 168 patients.
Results: Kaplan–Meier
survival analyses of both cohorts revealed that CCRCC patients with high SIRI
levels exhibited poorer overall survival (OS) and cancer-specific survival
(CSS) compared with those with low SIRI levels. Furthermore, univariate and
multivariate analyses identified SIRI as a significant independent predictor
for both OS (HR: 4.853; 95% CI: 2.362–9.972; P <0.001) and CSS
(HR: 5.913; 95% CI: 2.681–13.040; P <0.001). Following propensity score matching
analysis, SIRI remained an excellent predictor for both OS and CSS. The area
under the curve for SIRI was larger than that of the platelet-to-lymphocyte
ratio (PLR), neutrophil-to-lymphocyte ratio (NLR), monocyte-to-lymphocyte ratio
(MLR), and Memorial Sloan Kettering Cancer Center (MSKCC) prognostic score in
both cohorts.
Conclusion: SIRI
might be a better prognostic predictor than PLR, NLR, MLR, and MSKCC score in
patients with localized or locally advanced CCRCC.
Institutional review board approval number: (2010)
Scientific Research Project No. 39
Keywords: systemic
inflammation response index, prognosis, clear cell renal cell carcinoma, PSM
