Table 3.
Author (Year) |
Reference | Patients (n) | Study Design | Cut-Off Value | Main Findings |
---|---|---|---|---|---|
Chovanec (2018) | [50] | 171 | Retrospective translational | 1003 | SII > 1003 highly correlated with intermediate and poor IGCCCG risk groups, bulky retroperitoneal lymphadenopathy, and elevated tumor markers SII > 1003 was associated with poor OS The combination of low PD-L1 expression and elevated SII correlated with poor prognosis |
Fankhauser (2018) | [40] | 146 | Retrospective cohort |
1428 | SII > 1428 was significantly associated with poor OS |
Imamoglu (2019) | [45] | 112 | Retrospective cohort |
672 | SII > 672 was associated with an advanced disease stage |
Cursano (2020) | [42] | 62 | Retrospective cohort |
844 | SII > 844 highly correlated with worse OS and PFS SII > 844 was associated with poor response to CHT |
Yoshinaga (2020) | [47] | 63 | Retrospective cohort |
- | SII was not associated with OS |
Bumbasirevic (2022) | [39] | 88 | Prospective cohort |
683.21 | Median SII values were significantly lower in Stage I patients compared with Stage II and III patients SII > 683.21 was associated of metastatic disease development SII was associated with 8-hydroxydeoxyguanosine, a representative byproduct of oxidative DNA damage |
Kalavska (2022) | [49] | 51 | Retrospective cohort |
1003 | SII > 1003 was associated with an increased percentage of neutrophils and decreased percentage of lymphocytes |
SII, systemic immune-inflammation index; IGCCCG, International Germ Cell Cancer Collaborative Group; OS, overall survival; PFS, progression-free survival; CHT, chemotherapy; PD-L1, programmed death-ligand 1.