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Competing Risk Bias in Prognostic Models Predicting Hepatocellular Carcinoma Occurrence: Impact on Clinical Decision-making.
Innes, Hamish; Johnson, Philip; McDonald, Scott A; Hamill, Victoria; Yeung, Alan; Dillon, John F; Hayes, Peter C; Went, April; Barclay, Stephen T; Fraser, Andrew; Bathgate, Andrew; Goldberg, David J; Hutchinson, Sharon J.
Affiliation
  • Innes H; School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, UK.
  • Johnson P; Public Health Scotland, Glasgow, UK.
  • McDonald SA; Division of Epidemiology and Public Health, University of Nottingham, Nottingham, UK.
  • Hamill V; Department of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
  • Yeung A; School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, UK.
  • Dillon JF; Public Health Scotland, Glasgow, UK.
  • Hayes PC; School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, UK.
  • Went A; Public Health Scotland, Glasgow, UK.
  • Barclay ST; School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, UK.
  • Fraser A; Public Health Scotland, Glasgow, UK.
  • Bathgate A; Division of Molecular and Clinical Medicine, School of Medicine, University of Dundee, Dundee, UK.
  • Goldberg DJ; Royal Infirmary of Edinburgh, Edinburgh, UK.
  • Hutchinson SJ; Public Health Scotland, Glasgow, UK.
Gastro Hep Adv ; 1(2): 129-136, 2022.
Article in En | MEDLINE | ID: mdl-39131124
ABSTRACT
Background and

Aims:

Existing models predicting hepatocellular carcinoma (HCC) occurrence do not account for competing risk events and, thus, may overestimate the probability of HCC. Our goal was to quantify this bias for patients with cirrhosis and cured hepatitis C.

Methods:

We analyzed a nationwide cohort of patients with cirrhosis and cured hepatitis C infection from Scotland. Two HCC prognostic models were developed (1) a Cox regression model ignoring competing risk events and (2) a Fine-Gray regression model accounting for non-HCC mortality as a competing risk. Both models included the same set of prognostic factors used by previously developed HCC prognostic models. Two predictions were calculated for each patient first, the 3-year probability of HCC predicted by model 1 and second, the 3-year probability of HCC predicted by model 2.

Results:

The study population comprised 1629 patients with cirrhosis and cured HCV, followed for 3.8 years on average. A total of 82 incident HCC events and 159 competing risk events (ie, non-HCC deaths) were observed. The mean predicted 3-year probability of HCC was 3.37% for model 1 (Cox) and 3.24% for model 2 (Fine-Gray). For most patients (76%), the difference in the 3-year probability of HCC predicted by model 1 and model 2 was minimal (ie, within 0 to ±0.3%). A total of 2.6% of patients had a large discrepancy exceeding 2%; however, these were all patients with a 3-year probability exceeding >5% in both models.

Conclusion:

Prognostic models that ignore competing risks do overestimate the future probability of developing HCC. However, the degree of overestimation-and the way it is patterned-means that the impact on HCC screening decisions is likely to be modest.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Gastro Hep Adv / Gastro Hep advances Year: 2022 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Gastro Hep Adv / Gastro Hep advances Year: 2022 Type: Article