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Authors Sun Y, Li W, Li AJ, Su H, Yue J, Yu J
Received 10 October 2018
Accepted for publication 7 March 2019
Published 11 April 2019 Volume 2019:11 Pages 3153—3162
DOI https://doi.org/10.2147/CMAR.S190335
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Ms Justinn Cochran
Peer reviewer comments 3
Editor who approved publication: Dr Rituraj Purohit
Purpose: We sought
to examine the role of pretreatment systemic immune-inflammation index (SII) in
hormone receptor-negative, human epidermal growth factor receptor 2+ (HER2+)
breast cancer patients.
Patients and methods: 155 HER2+
patients treated in our hospital from September 3, 2002, to September 21, 2012,
were retrospectively enrolled. SII was established as neutrophil x
platelet/lymphocyte counts. The median value of SII was used as cut-off value.
We used the Kaplan-Meier method to evaluate the overall survival (OS),
disease-free survival (DFS), distant metastasis-free survival (DMFS). To
comparatively evaluate the survival rates between patients from two groups, we
used the log-rank test. For identifying independent factors of prognosis, we
used the Cox regression model, applying multivariate statistics.
Results: Analyses
show that HER2+ patients with high and low SII had median DFS of 15.1 and
31.5 months, respectively (P <0.001), while the median DMFS in HER2+ patients
with high SII was 18.4 and in patients with low SII was 33.0 months (P =0.001), and the
median OS were 54.5 and 71.1 months respectively in high and low SII
patients, respectively (P =0.002). Multivariate analysis had revealed increased
SII independently linked to poor DFS (HR =1.46, 95% CI: 1.01–2.11, P =0.045). The
difference between SII and DMFS bore no statistical significance. (HR =1.40,
95% CI: 0.96–2.03, P =0.078), while high SII independently predicted short
OS (HR =1.51, 95% CI: 1.02–2.25, P =0.038).
Conclusion: Our
findings suggest that increased SII independently predicts poor survival for
hormone receptor-negative, HER2+ breast cancer patients. Prospective studies
are, however, required to confirm the role of SII in the prognosis of patients
with HER2+ before clinical use.
Keywords: breast
cancer, SII, HER2, inflammation
