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Outcomes after cancer diagnosis in children and adult patients with congenital heart disease in Sweden: a registry-based cohort study.
Karazisi, Christina; Dellborg, Mikael; Mellgren, Karin; Giang, Kok Wai; Skoglund, Kristofer; Eriksson, Peter; Mandalenakis, Zacharias.
Afiliación
  • Karazisi C; Department of Molecular and Clinical Medicine, University of Gothenburg, Goteborg, Sweden christina.karazisi@vgregion.se.
  • Dellborg M; Department of Medicine, Geriatrics and Emergency Medicine, Region Västra Götaland, Sahlgrenska University Hospital, Goteborg, Sweden.
  • Mellgren K; Department of Molecular and Clinical Medicine, University of Gothenburg, Goteborg, Sweden.
  • Giang KW; Department of Medicine, Geriatrics and Emergency Medicine, Region Västra Götaland, Sahlgrenska University Hospital, Goteborg, Sweden.
  • Skoglund K; Adult Congenital Heart Disease Unit, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Eriksson P; Department of Pediatric Oncology, Sahlgrenska University Hospital, Goteborg, Sweden.
  • Mandalenakis Z; Department of Molecular and Clinical Medicine, University of Gothenburg, Goteborg, Sweden.
BMJ Open ; 14(4): e083237, 2024 Apr 17.
Article en En | MEDLINE | ID: mdl-38631823
ABSTRACT

OBJECTIVE:

Patients with congenital heart disease (CHD) have an increased cancer risk. The aim of this study was to determine cancer-related mortality in CHD patients compared with non-CHD controls, compare ages at cancer diagnosis and death, and explore the most fatal cancer diagnoses.

DESIGN:

Registry-based cohort study. SETTING AND

PARTICIPANTS:

CHD patients born between 1970 and 2017 were identified using Swedish Health Registers. Each was matched by birth year and sex with 10 non-CHD controls. Included were those born in Sweden with a cancer diagnosis.

RESULTS:

Cancer developed in 758 out of 67814 CHD patients (1.1%), with 139 deaths (18.3%)-of which 41 deaths occurred in patients with genetic syndromes. Cancer was the cause of death in 71.9% of cases. Across all CHD patients, cancer accounted for 1.8% of deaths. Excluding patients with genetic syndromes and transplant recipients, mortality risk between CHD patients with cancer and controls showed no significant difference (adjusted HR 1.17; 95% CI 0.93 to 1.49). CHD patients had a lower median age at cancer diagnosis-13.0 years (IQR 2.9-30.0) in CHD versus 24.6 years (IQR 8.6-35.1) in controls. Median age at death was 15.1 years (IQR 3.6-30.7) in CHD patients versus 18.5 years (IQR 6.1-32.7) in controls. The top three fatal cancer diagnoses were ill-defined, secondary and unspecified, eye and central nervous system tumours and haematological malignancies.

CONCLUSIONS:

Cancer-related deaths constituted 1.8% of all mortalities across all CHD patients. Among CHD patients with cancer, 18.3% died, with cancer being the cause in 71.9% of cases. Although CHD patients have an increased cancer risk, their mortality risk post-diagnosis does not significantly differ from non-CHD patients after adjustements and exclusion of patients with genetic syndromes and transplant recipients. However, CHD patients with genetic syndromes and concurrent cancer appear to be a vulnerable group.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cardiopatías Congénitas / Neoplasias Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans País/Región como asunto: Europa Idioma: En Revista: BMJ Open Año: 2024 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cardiopatías Congénitas / Neoplasias Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans País/Región como asunto: Europa Idioma: En Revista: BMJ Open Año: 2024 Tipo del documento: Article País de afiliación: Suecia