So sánh phương pháp

	Phân tích Rủi ro Cạnh tranh Đa trung tâm	Hồi quy Cox Tỷ lệ Tử vong Tỷ lệ Tăng dần Đa trung tâm
Lĩnh vực	Dịch tễ học	Dịch tễ học
Họ	Process / pipeline	Process / pipeline
Năm ra đời	1999 (Fine-Gray); extended to multicenter settings throughout 2000s–2010s	1972 (Cox model); multicenter applications formalized 1980s–1990s
Người khởi xướng	Fine & Gray (subdistribution hazard model); Prentice et al. (cause-specific hazard model)	D. R. Cox (Cox PH model); multicenter extension developed through collaborative trial methodology
Loại	Survival / time-to-event statistical analysis	Semi-parametric survival regression for clustered data
Công trình gốc	Fine, J. P., & Gray, R. J. (1999). A proportional hazards model for the subdistribution of a competing risk. Journal of the American Statistical Association, 94(446), 496–509.	Cox, D. R. (1972). Regression models and life-tables. Journal of the Royal Statistical Society: Series B (Methodological), 34(2), 187–202.
Tên gọi khác	multicenter CRA, multi-site competing risks, multicenter cumulative incidence analysis, polycentric competing risks study	multicenter Cox regression, multisite Cox PH model, stratified Cox model across centers, multicenter survival regression
Liên quan	4	4
Tóm tắt	Multicenter competing risks analysis is a time-to-event method applied across multiple clinical centers to estimate the probability of a specific event of interest when other mutually exclusive events — competing risks — can preclude its occurrence. By pooling data from diverse sites, it achieves the sample sizes needed to model rare events and enables assessment of center-level variation in cumulative incidence and covariate effects.	Multicenter Cox proportional hazards regression extends the classic Cox PH model to studies conducted at two or more clinical sites or centers. It estimates the effect of predictors on time-to-event outcomes while explicitly accounting for clustering within centers, between-center heterogeneity, and potential differences in baseline hazard across sites. This design is standard practice in large multicenter RCTs and observational cohort studies in oncology, cardiology, and other clinical fields.