DataSheet1.pdf

Abstract

Objectives: The present study aimed to identify the predictive value of inflammatory indexes stratified according to human papillomavirus (HPV) infection status in women with FIGO 2018 stage IB~IIA cervical cancer. We also explored the influences of HPV infection status on the survival of cervical cancer patients. Methods: We collected data for 583 women with stage IB~IIA cervical cancer in Sun Yat-sen University Cancer Center between 2009 and 2017. The t-test, chi-squared (χ2) test and Fisher’s exact test were applied to compare the differences of inflammatory indexes and clinicopathological features between HPV-positive and HPV-negative groups. Univariate and multivariate analyses were used to identify clinicopathological factors that were associated with the prognosis of cervical cancer patients. Results: There were no differences in overall survival (OS) and progression-free survival (PFS) between HPV-positive and HPV-negative groups. In HPV-positive group, the maximum tumor size, neoadjuvant chemotherapy and the body mass index (BMI) correlated significantly with C-reactive protein/albumin ratio (CAR). The maximum tumor size and the prognostic nutritional index (PNI) correlated significantly with the platelet lymphocyte ratio (PLR). The maximum tumor size, neoadjuvant chemotherapy and PLR correlated significantly with PNI. Univariate and multivariate analyses showed that the depth of tumor invasion (HR:3.651, 95%CI:1.464-9.103, P=0.005; HR:2.478, 95%CI:1.218-5.043, P=0.012) and CAR (HR:5.201, 95%CI:2.080-13.004, P<0.0001; HR:2.769, 95%CI:1.406-5.455, P=0.003) were independent predictors of poor OS and PFS. PNI was an independent protective factor of OS (HR:0.341, 95%CI:0.156-0.745, P=0.007). PLR was an independent factor of PFS (HR:1.991, 95%CI:1.018-3.894, P=0.044). In HPV-negative group, BMI correlated significantly with CAR. Only depth of invasion (HR:9.192, 95%CI:1.016-83.173, P=0.048) was the independent predictor of poor OS, and no inflammation indexes were independent predictors of prognosis. Conclusions: In patients with HPV-positive cervical cancer, depth of invasion, PNI and CAR are independent factors of OS, and depth of invasion, PLR and CAR are independent factors for PFS. For patients with HPV-negative disease, no inflammation indexes had predictive value for prognosis. The predictive value of inflammation indexes on prognosis is more significant in patients with HPV-positive cervical cancer. Stratification of HPV infection status promotes a more precise clinical application of inflammation indexes, thus improving their accuracy and feasibility.