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Multiple imputation for missing values in ordinal variables from cancer registry data when performing Cox proportional hazards regression
by
Hüsing, Anika
, Hoffmann, Wolfgang
, Hüsing, Johannes
, Kästner, Anika
, Stang, Andreas
in
Analysis
/ Bias
/ Cancer
/ Cancer therapies
/ Chemotherapy
/ Computer Simulation
/ Health care
/ Health Sciences
/ Humans
/ Imputation
/ Information management
/ Logistic Models
/ Lung cancer
/ Lung Neoplasms - epidemiology
/ Medicine
/ Medicine & Public Health
/ Methods
/ Missing data
/ Neoplasms
/ Oncology
/ Oncology, Experimental
/ Proportional Hazards Models
/ Random Forest
/ Registries
/ Registries (in medicine)
/ Registries - statistics & numerical data
/ Regression analysis
/ Simulation
/ Statistical Theory and Methods
/ Statistics for Life Sciences
/ Surgery
/ Survival analysis
/ Theory of Medicine/Bioethics
/ Variables
2026
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Multiple imputation for missing values in ordinal variables from cancer registry data when performing Cox proportional hazards regression
by
Hüsing, Anika
, Hoffmann, Wolfgang
, Hüsing, Johannes
, Kästner, Anika
, Stang, Andreas
in
Analysis
/ Bias
/ Cancer
/ Cancer therapies
/ Chemotherapy
/ Computer Simulation
/ Health care
/ Health Sciences
/ Humans
/ Imputation
/ Information management
/ Logistic Models
/ Lung cancer
/ Lung Neoplasms - epidemiology
/ Medicine
/ Medicine & Public Health
/ Methods
/ Missing data
/ Neoplasms
/ Oncology
/ Oncology, Experimental
/ Proportional Hazards Models
/ Random Forest
/ Registries
/ Registries (in medicine)
/ Registries - statistics & numerical data
/ Regression analysis
/ Simulation
/ Statistical Theory and Methods
/ Statistics for Life Sciences
/ Surgery
/ Survival analysis
/ Theory of Medicine/Bioethics
/ Variables
2026
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Multiple imputation for missing values in ordinal variables from cancer registry data when performing Cox proportional hazards regression
by
Hüsing, Anika
, Hoffmann, Wolfgang
, Hüsing, Johannes
, Kästner, Anika
, Stang, Andreas
in
Analysis
/ Bias
/ Cancer
/ Cancer therapies
/ Chemotherapy
/ Computer Simulation
/ Health care
/ Health Sciences
/ Humans
/ Imputation
/ Information management
/ Logistic Models
/ Lung cancer
/ Lung Neoplasms - epidemiology
/ Medicine
/ Medicine & Public Health
/ Methods
/ Missing data
/ Neoplasms
/ Oncology
/ Oncology, Experimental
/ Proportional Hazards Models
/ Random Forest
/ Registries
/ Registries (in medicine)
/ Registries - statistics & numerical data
/ Regression analysis
/ Simulation
/ Statistical Theory and Methods
/ Statistics for Life Sciences
/ Surgery
/ Survival analysis
/ Theory of Medicine/Bioethics
/ Variables
2026
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Multiple imputation for missing values in ordinal variables from cancer registry data when performing Cox proportional hazards regression
Journal Article
Multiple imputation for missing values in ordinal variables from cancer registry data when performing Cox proportional hazards regression
2026
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Overview
Background
Scientists working with cancer registry data are often confronted with large proportions of missing values in ordinal variables, such as tumor stage, grading or the general health status (ECOG-PS scored 0 to 5). Despite the long-standing issue, research on handling missing ordinal cancer registry data remains sparse.
Methods
A simulation study was conducted using complete lung cancer cases (2019–2022) from the North Rhine-Westphalia Cancer Registry. Missing values in ECOG-PS were generated with varying missingness mechanisms (MCAR, MAR, MNAR), missingness proportions (10% to 50%) and sample sizes (
N
= 500,
N
= 1,000,
N
= 5,000). The data were then replaced using MICE with ordinal logistic regression (POLR), multinomial regression (POLYREG), predictive mean matching (PMM), random forests (RF), and the joint model (JM). The performance parameters bias, MSE, width of the 95%CI and coverage were assessed.
Results
Severe bias, high MSE, wide 95%CI, and poor coverage were found in scenarios with sample sizes of
N
= 500 and 1,000 and 30% or more missing data with low prevalence of ECOG-PS = 4. MICE with POLYREG maintained low bias across all scenarios with
N
= 5,000, while MICE with RF and PMM performed well with up to 30%-50% missing data. MICE with POLR and the JM yielded low bias with up to 10%-20% missing data. Compared to complete case analysis, MI did not offer a systematic advantage in terms of bias or MSE compared to the MI methods evaluated.
Conclusion
Sample size and ordinal category distribution impact missing data handling in registry studies. Severe bias might be introduced when sample sizes are smaller and prevalence of categories is low, indicating finite-sample effects rather than systematic bias of the imputation methods. Among the MI methods applied, MICE with POLYREG performed best, however, further research is needed for time-to-event analyses and multivariate missingness patterns.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
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