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Research · 03 of 05

Childhood cancer survivors had two and a half times the cardiovascular risk of peers

Treat childhood cancer survivorship as a lifelong cardiovascular risk and hand it over at transition.

Design
Systematic review and meta-analysis of cohort studies
Population
39 cohorts: 536,399 CAYA cancer survivors and 1,810,572 cancer-free peers
Primary outcome
Incident cardiovascular disease
Effect
RR 1.99 (1.66–2.40); childhood cancer RR 2.48 (1.87–3.27); young adult RR 1.61 (1.37–1.88)

A meta-analysis in JAMA Pediatrics (28 September) pooled 39 cohort studies including 536,399 people who had cancer in childhood, adolescence or young adulthood and 1.8 million cancer-free peers.

Survivors had about twice the risk of cardiovascular disease overall (RR 1.99, 95% CI 1.66 to 2.40), an estimated 90 extra events per 1,000 survivors. The relative risk was higher for cancer in childhood (RR 2.48) than in young adulthood (RR 1.61). It narrowed with longer follow-up but remained raised beyond 20 years, and held in high-quality and population-based analyses.

For paediatricians and the GPs who inherit these patients, the message is that cardiovascular risk follows a childhood cancer into adult life. Survivorship care should include blood pressure, lipids, glucose and weight, and knowledge of which treatments — anthracyclines and chest radiation in particular — carry specific cardiac surveillance needs.

  • Keep a treatment summary for every childhood cancer survivor, including anthracycline dose and radiation fields.
  • Check blood pressure, lipids, glucose and weight regularly through survivorship.
  • Follow survivorship guidance for echocardiographic surveillance after cardiotoxic treatment.
  • Hand over cardiovascular risk explicitly at transition to adult care.

Why it matters

Risk persists for decades, well past the point when survivors leave paediatric follow-up.

The statistics, in plain English

A risk ratio of 1.99 means about double the rate. The 90 extra events per 1,000 is an absolute estimate over the studies' follow-up and depends on baseline risk. These are cohort data, so part of the excess may reflect factors other than the cancer treatment.

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