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Home›Epidemiology›Multicenter Competing Risks Analysis
Process / pipelineClinical / epidemiology

Multicenter Competing Risks Analysis

Also known as: multicenter CRA, multi-site competing risks, multicenter cumulative incidence analysis, polycentric competing risks study

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.

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Multicenter Competing Risks Analysis
Cox proportional hazardsKaplan-Meier AnalysisMulticenter cohort studyMulticenter Cox proporti…

When to use it

Use multicenter competing risks analysis when: (1) the primary outcome can be precluded by one or more alternative events (e.g., cause-specific mortality, graft failure when death before graft failure is a competing risk); (2) single-center sample sizes are insufficient for the event rate; and (3) generalizability across patient populations or healthcare systems is a study aim. This design is particularly valuable for rare diseases, post-marketing safety studies, and registry-based comparative effectiveness research. Do NOT use it when all patients experience the same type of event with no competing risks — standard survival analysis suffices. Do NOT apply the Fine-Gray model for etiological questions about risk factor effects; use cause-specific hazard models instead. Do NOT ignore center heterogeneity in analysis.

Strengths & limitations

Strengths
  • Correctly estimates the absolute probability of the event of interest in the presence of competing events, avoiding the overestimation bias of Kaplan-Meier.
  • Pooling across centers yields sufficient power to study rare outcomes and to estimate covariate effects in subgroups.
  • Enables assessment of center-level variation in cumulative incidence, supporting quality improvement and comparative effectiveness analyses.
  • Well-supported by mature statistical theory (Aalen-Johansen estimator, Fine-Gray model) and widely available software (R cmprsk, SAS, Stata stcompet).
  • Provides results directly interpretable as absolute probabilities, which are more clinically meaningful than hazard ratios alone.
Limitations
  • Requires strict harmonization of event definitions and follow-up rules across centers; even small definitional differences can bias pooled estimates.
  • Cluster adjustment methods (stratification, frailty models) add analytical complexity and require decisions that affect results.
  • The Fine-Gray model's subdistribution hazard has a complex interpretation and does not estimate the cause-specific hazard; both models should typically be reported.
  • Data sharing across institutions raises privacy, regulatory, and logistical barriers that can delay or limit the study.
  • Proportionality assumptions of regression models must be verified for each event type and center.

Frequently asked

Why can I not just use Kaplan-Meier and treat competing events as censored?

Kaplan-Meier assumes that censored individuals have the same future risk as those still under observation. Competing events violate this assumption because a patient who dies from another cause truly cannot experience the primary event. Treating them as censored overestimates the cumulative incidence of the primary event. The Aalen-Johansen estimator and the Fine-Gray model avoid this by explicitly accounting for the probability mass absorbed by competing events.

When should I use the Fine-Gray model versus the cause-specific Cox model?

Use the Fine-Gray subdistribution hazard model when your primary question is about absolute risk — the probability that a patient with given characteristics will experience the event by a particular time, factoring in competing risks. Use cause-specific Cox models when your question is etiological — whether a risk factor accelerates the biological process leading to the event, independent of competing events. In most multicenter clinical studies, both should be reported.

How should I account for center effects?

The most common approaches are stratification (allowing each center its own baseline hazard), inclusion of a center fixed effect as a covariate, robust sandwich standard errors clustered at the center level, and random-effects frailty models. Stratification is preferred when center-specific baseline hazards are expected to differ substantially; frailty models are preferred when the number of centers is large and center effects are of scientific interest.

What sample size is needed for a multicenter competing risks study?

Sample size depends on the expected cumulative incidence of the primary event (not the overall event rate), the number of covariates in the model, and the degree of clustering. Rules of thumb from cause-specific Cox regression (roughly 10–15 events per covariate) provide a starting point, but simulation-based power calculations using the Fine-Gray model are preferred when competing event rates are substantial.

Can I use federated or distributed analysis instead of pooling individual patient data?

Yes. Meta-analytic approaches (analyzing center-level summary statistics and pooling estimates) and federated learning frameworks that compute gradients or sufficient statistics locally are viable when data sharing is legally or logistically infeasible. However, federated approaches for the Fine-Gray model require specialized algorithms and may lose some efficiency relative to individual patient data pooling.

Sources

  1. 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. DOI: 10.1080/01621459.1999.10474144 ↗
  2. Austin, P. C., Lee, D. S., & Fine, J. P. (2016). Introduction to the analysis of survival data in the presence of competing risks. Circulation, 133(6), 601–609. DOI: 10.1161/CIRCULATIONAHA.115.017719 ↗

How to cite this page

ScholarGate. (2026, June 3). Multicenter Competing Risks Analysis. ScholarGate. https://scholargate.app/en/epidemiology/multicenter-competing-risks-analysis

Related methods

Cox proportional hazardsKaplan-Meier AnalysisMulticenter cohort studyMulticenter Cox proportional hazards

Which method?

Set this method beside its closest kin and read them side by side — the library lays the books on the table; the choice is yours.

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Similar methods

Prospective Competing Risks AnalysisRetrospective competing risks analysisRisk-adjusted competing risks analysisCompeting Risks AnalysisMatched Competing Risks AnalysisAdaptive Competing Risks AnalysisFine-Gray Competing Risks ModelMeta-analytic competing risks analysis

Related reference concepts

Competing RisksSurvival Analysis and Time-to-Event MethodsCox Regression ModelsCensoring and Follow-Up DataKaplan-Meier Survival CurvesProportional Hazards Assumption

Spotted an issue on this page? Report or suggest a fix →

ScholarGate — Multicenter Competing Risks Analysis (Multicenter Competing Risks Analysis). Retrieved 2026-07-21 from https://scholargate.app/en/epidemiology/multicenter-competing-risks-analysis · Dataset: https://doi.org/10.5281/zenodo.20539026
Quick facts
Originator
Fine & Gray (subdistribution hazard model); Prentice et al. (cause-specific hazard model)
Year
1999 (Fine-Gray); extended to multicenter settings throughout 2000s–2010s
Type
Survival / time-to-event statistical analysis
DataType
Time-to-event data with event type indicators, center identifiers, and covariates from multiple clinical sites
Subfamily
Clinical / epidemiology
Related methods
Cox proportional hazardsKaplan-Meier AnalysisMulticenter cohort studyMulticenter Cox proportional hazards
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