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Incidence and survival of pediatric and adult hepatocellular carcinoma, United States, 2001-2020.
Arnett, Azlann; Siegel, David A; Dai, Shifan; Thompson, Trevor D; Foster, Jennifer; di Pierro, Erika J; Momin, Behnoosh; Lupo, Philip J; Heczey, Andras.
Afiliação
  • Arnett A; Cancer and Hematology Centers, Texas Children's Hospital, Houston, Texas.
  • Siegel DA; Division of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
  • Dai S; Division of Cancer Prevention and Control, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Thompson TD; Cyberdata Technologies, Inc., Herndon, Virginia.
  • Foster J; Division of Cancer Prevention and Control, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • di Pierro EJ; Cancer and Hematology Centers, Texas Children's Hospital, Houston, Texas.
  • Momin B; Division of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
  • Lupo PJ; Cancer and Hematology Centers, Texas Children's Hospital, Houston, Texas.
  • Heczey A; Division of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
medRxiv ; 2024 Apr 05.
Article em En | MEDLINE | ID: mdl-38633779
ABSTRACT
Importance Hepatocellular carcinoma accounts for approximately 80% of liver neoplasms. Globally, hepatocellular carcinoma ranks as the third most lethal cancer, with the number of deaths expected to further increase by 2040. In adults, disparities in incidence and survival are well described while pediatric epidemiology is not well characterized.

Objective:

To describe incidence and survival for pediatric (ages 0-19 years) hepatocellular carcinoma cases and compare these measures to adults (ages ≥20 years) diagnosed with hepatocellular carcinoma. We evaluated demographic factors and clinical characteristics that influence incidence and outcomes.

Design:

Population-based cohort study.

Setting:

Incidence data from the US Cancer Statistics database from 2003 to 2020 and 5-year relative survival from the National Program of Cancer Registries from 2001 to 2019, covering 97% and 83% of the US population, respectively.

Participants:

355,349 US Cancer Statistics and 257,406 the National Program of Cancer Registries patients were identified using ICD-O-3 C22.0 and 8170-5 codes. Main Outcomes and

Measures:

Incidence annual percent change (APC) and average APC (AAPC) using joinpoint regression. Five-year relative survival. All-cause survival estimated using multivariate Cox modeling. Corresponding 95% confidence intervals (CI) were calculated.

Results:

Incidence rate per 100,000 persons was 0.056 (95%CI0.052-0.060) for pediatric cases and 7.793 (7.767-7.819) for adults. Incidence was stable in the pediatric population (0.3 AAPC, -1.1-1.7). In contrast, after periods of increase, incidence declined in adults after 2015 (-1.5 APC). Relative survival increased over time for both pediatric and adult ages and was higher for children and adolescents (46.4%, 95%CI42.4-50.3) than adults (20.7%, 95%CI20.5-20.9) overall and when stratified by stage. Regression modeling showed that non-Hispanic Black race and ethnicity was associated with higher risk of death in children and adolescents (1.48, 95%CI1.07-2.05) and adults (1.11, 95%CI1.09-1.12) compared to non-Hispanic white race and ethnicity. Conclusions and Relevance Between 2003 and 2020 in the United States, pediatric incidence was stable while incidence in adults began to decline after 2015. Survival was higher across all stages for children and adolescents compared to adults. Non-Hispanic Black race and ethnicity showed a higher risk of death for both age groups. Further studies could explore the factors that influence these outcome disparities.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: MedRxiv Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: MedRxiv Ano de publicação: 2024 Tipo de documento: Article