Cancer mortality in children surviving congenital heart interventions: A study from the Pediatric Cardiac Care Consortium.

IF 2.4 3区 医学 Q2 HEMATOLOGY Pediatric Blood & Cancer Pub Date : 2024-08-13 DOI:10.1002/pbc.31271
Amanda S Thomas, Logan G Spector, Courtney McCracken, Matthew E Oster, Lazaros K Kochilas
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Abstract

Introduction: Children with congenital heart defects (CHD) have shorter life expectancy than the general population. Previous studies also suggest that patients with CHD have higher risk of cancer. This study aims to describe cancer-related mortality among patients with a history of CHD interventions using the Pediatric Cardiac Care Consortium (PCCC), a large US cohort of such patients.

Methods: We performed a retrospective cohort study of individuals (<21 years) who underwent interventions for CHD in the PCCC from 1982 to 2003. Patients surviving their first intervention were linked to the National Death Index through 2020. Multivariable models assessed risk of cancer-related death, adjusting for age, sex, race, and ethnicity. Patients with/without genetic abnormalities (mostly Down syndrome [DS]) were considered separately, due to expected differential risk in cancer.

Results: Among the 57,601 eligible patients in this study, cancer was the underlying or contributing cause of death for 208; with 20% among those with DS. Significantly increased risk of cancer-related death was apparent among patients with DS compared to the non-genetic group (aHR: 3.63, 95% confidence interval [CI]: 2.52-5.24, p < .001). For the group with non-genetic abnormalities, the highest association with cancer-related death compared to those with mild CHD was found among those with more severe CHD (severe two-ventricle aHR: 1.82, 95% CI: 1.04-3.20, p = .036, single-ventricle aHR: 4.68, 95% CI: 2.77-7.91, p < .001).

Conclusions: Patients with more severe forms of CHD are at increased risk for cancer-related death. Despite our findings, we are unable to distinguish whether having CHD raises the risk of cancer or reduces survival.

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先天性心脏病介入术后存活儿童的癌症死亡率:儿科心脏护理联盟的一项研究。
导言:患有先天性心脏缺陷(CHD)的儿童的预期寿命比普通人短。以往的研究还表明,先天性心脏病患者罹患癌症的风险较高。本研究的目的是利用儿科心脏护理联盟(PCCC)这一美国大型此类患者队列来描述有先天性心脏病干预史的患者的癌症相关死亡率:我们对患者进行了一项回顾性队列研究(Results:在这项研究的 57,601 名符合条件的患者中,208 人的根本死因或诱因是癌症;其中 20% 是 DS 患者。与非遗传组相比,DS 患者癌症相关死亡风险明显增加(aHR:3.63,95% 置信区间 [CI]:2.52-5.24,p 结论:与非遗传组相比,DS 患者癌症相关死亡风险明显增加(aHR:3.63,95% 置信区间 [CI]:2.52-5.24,p 结论):患有较严重先天性心脏病的患者发生癌症相关死亡的风险较高。尽管我们有这样的发现,但仍无法区分患有先天性心脏病是会增加患癌风险还是会降低生存率。
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来源期刊
Pediatric Blood & Cancer
Pediatric Blood & Cancer 医学-小儿科
CiteScore
4.90
自引率
9.40%
发文量
546
审稿时长
1.5 months
期刊介绍: Pediatric Blood & Cancer publishes the highest quality manuscripts describing basic and clinical investigations of blood disorders and malignant diseases of childhood including diagnosis, treatment, epidemiology, etiology, biology, and molecular and clinical genetics of these diseases as they affect children, adolescents, and young adults. Pediatric Blood & Cancer will also include studies on such treatment options as hematopoietic stem cell transplantation, immunology, and gene therapy.
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