<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Dong M</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Previous studies on the systemic immune-inflammation index (SII), which is based on platelet, neutrophil and lymphocyte counts, as a prognostic marker in patients with colorectal cancer (CRC) yielded inconsistent results. The aim of this study was to evaluate the prognostic and clinicopathological role of SII in CRC &lt;i>via&lt;/i> meta-analysis.&lt;h4>Methods&lt;/h4>A comprehensive literature survey was performed on PubMed, Web of Science, Embase and the Cochrane Library databases to include studies published up to 6 April 2020. Pooled hazard ratios (HRs) and odds ratios (ORs) with 95% confidence intervals (CIs) were computed to estimate the prognostic and clinicopathological value of SII in CRC.&lt;h4>Results&lt;/h4>A total of 12 studies published between 2016 and 2019 were included in our meta-analysis. The combined analysis showed that high SII levels were significantly associated with worse overall survival (OS; HR = 1.61, 95% CI = 1.21-2.13, &lt;i>p&lt;/i> = 0.001) and progression-free survival (HR = 1.74, 95% CI = 1.26-2.39, &lt;i>p&lt;/i> = 0.001) in CRC. Moreover, elevated SII was also correlated with poor tumor differentiation (OR = 1.60, 95% CI = 1.27-2.02, &lt;i>p&lt;/i> &lt; 0.001), presence of distant metastasis (OR = 2.27, 95% CI = 1.10-4.67, &lt;i>p&lt;/i> = 0.026), ECOG PS of 1-2 (OR = 1.98, 95% CI = 1.39-2.84, &lt;i>p&lt;/i> &lt; 0.001) and tumor size ⩾5 cm (OR = 1.49, 95% CI = 1.18-1.88, &lt;i>p&lt;/i> = 0.001). However, high SII was not significantly associated with sex, tumor location, lymph node metastasis, or age in patients with CRC.&lt;h4>Conclusion&lt;/h4>Our meta-analysis indicated that high SII levels predicted poor prognosis in CRC. In addition, an elevated SII was also associated with clinical factors, implying higher malignancy of the disease.</pubmed_abstract><journal>Therapeutic advances in medical oncology</journal><pagination>1758835920937425</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7357045</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Prognostic and clinicopathological significance of systemic immune-inflammation index in colorectal cancer: a meta-analysis.</pubmed_title><pmcid>PMC7357045</pmcid><pubmed_authors>Mi Y</pubmed_authors><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Zhou Q</pubmed_authors><pubmed_authors>Gu X</pubmed_authors><pubmed_authors>Lian Y</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Wang D</pubmed_authors><pubmed_authors>Dong M</pubmed_authors><pubmed_authors>Ma T</pubmed_authors><pubmed_authors>Fan R</pubmed_authors><pubmed_authors>Shi Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prognostic and clinicopathological significance of systemic immune-inflammation index in colorectal cancer: a meta-analysis.</name><description>&lt;h4>Background&lt;/h4>Previous studies on the systemic immune-inflammation index (SII), which is based on platelet, neutrophil and lymphocyte counts, as a prognostic marker in patients with colorectal cancer (CRC) yielded inconsistent results. The aim of this study was to evaluate the prognostic and clinicopathological role of SII in CRC &lt;i>via&lt;/i> meta-analysis.&lt;h4>Methods&lt;/h4>A comprehensive literature survey was performed on PubMed, Web of Science, Embase and the Cochrane Library databases to include studies published up to 6 April 2020. Pooled hazard ratios (HRs) and odds ratios (ORs) with 95% confidence intervals (CIs) were computed to estimate the prognostic and clinicopathological value of SII in CRC.&lt;h4>Results&lt;/h4>A total of 12 studies published between 2016 and 2019 were included in our meta-analysis. The combined analysis showed that high SII levels were significantly associated with worse overall survival (OS; HR = 1.61, 95% CI = 1.21-2.13, &lt;i>p&lt;/i> = 0.001) and progression-free survival (HR = 1.74, 95% CI = 1.26-2.39, &lt;i>p&lt;/i> = 0.001) in CRC. Moreover, elevated SII was also correlated with poor tumor differentiation (OR = 1.60, 95% CI = 1.27-2.02, &lt;i>p&lt;/i> &lt; 0.001), presence of distant metastasis (OR = 2.27, 95% CI = 1.10-4.67, &lt;i>p&lt;/i> = 0.026), ECOG PS of 1-2 (OR = 1.98, 95% CI = 1.39-2.84, &lt;i>p&lt;/i> &lt; 0.001) and tumor size ⩾5 cm (OR = 1.49, 95% CI = 1.18-1.88, &lt;i>p&lt;/i> = 0.001). However, high SII was not significantly associated with sex, tumor location, lymph node metastasis, or age in patients with CRC.&lt;h4>Conclusion&lt;/h4>Our meta-analysis indicated that high SII levels predicted poor prognosis in CRC. In addition, an elevated SII was also associated with clinical factors, implying higher malignancy of the disease.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2025-04-19T18:01:41.525Z</modification><creation>2025-04-19T18:01:41.525Z</creation></dates><accession>S-EPMC7357045</accession><cross_references><pubmed>32699557</pubmed><doi>10.1177/1758835920937425</doi></cross_references></HashMap>