Department of Molecular and Clinical Medicine, University of Gothenburg, Goteborg, Sweden
Department of Medicine, Geriatrics and Emergency Medicine, Region Västra Götaland, Sahlgrenska University Hospital, Goteborg, Sweden.
BMJ Open. 2024 Apr 17;14(4):e083237. doi: 10.1136/bmjopen-2023-083237.
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.
Registry-based cohort study.
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.
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.
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.
先天性心脏病(CHD)患者的癌症风险增加。本研究旨在确定 CHD 患者与非 CHD 对照者相比的癌症相关死亡率,比较癌症诊断和死亡年龄,并探讨最致命的癌症诊断。
基于登记的队列研究。
使用瑞典健康登记册确定 1970 年至 2017 年间出生的 CHD 患者。每个患者都按照出生年份和性别与 10 名非 CHD 对照者相匹配。包括在瑞典出生并被诊断患有癌症的患者。
在 67814 例 CHD 患者中,有 758 例(1.1%)发生癌症,其中 139 例(18.3%)死亡-其中 41 例死亡发生在有遗传综合征的患者中。癌症是 71.9%病例的死亡原因。在所有 CHD 患者中,癌症占死亡人数的 1.8%。排除有遗传综合征和移植受者的患者后,CHD 患者癌症与对照组的死亡率无显著差异(调整后的 HR 1.17;95%CI 0.93 至 1.49)。CHD 患者的癌症诊断中位年龄较低-13.0 岁(IQR 2.9-30.0),而对照组为 24.6 岁(IQR 8.6-35.1)。CHD 患者的死亡中位年龄为 15.1 岁(IQR 3.6-30.7),而对照组为 18.5 岁(IQR 6.1-32.7)。最致命的三种癌症诊断为定义不明确、继发性和未特指、眼部和中枢神经系统肿瘤以及血液恶性肿瘤。
癌症相关死亡占所有 CHD 患者所有死亡人数的 1.8%。在患有癌症的 CHD 患者中,有 18.3%死亡,其中 71.9%的病例是癌症引起的。尽管 CHD 患者癌症风险增加,但调整后并排除有遗传综合征和移植受者的患者后,其诊断后死亡率与非 CHD 患者无显著差异。然而,有遗传综合征和并发癌症的 CHD 患者似乎是一个脆弱群体。