This focused, candidate-gene analysis identifies prognostic SNP-based subgroups and a nine-SNP polygenic risk score associated with survival in cervical cancer. While this work provides a foundation for immunogenetic risk stratification, the findings are derived from a limited SNP panel in a single cohort. Future validation in larger, independent cohorts with genome-wide data is required to confirm these preliminary genetic associations and to determine their relationship to broader molecular subgroups.
Zidi et al. (Fri,) studied this question.