Key result
Post-transplant statin use linked to ~67% lower risk of any malignancy.
Why the study?
Cancer remains a leading cause of death late after heart transplantation despite newer immunosuppressive agents, and the impact of statin therapy on cancer risk and mortality is unclear.
Does statin therapy reduce the occurrence of any malignancy in patients who survived the first year after heart transplantation?
Cohort (n=255)
No
Does statin therapy reduce the occurrence of any malignancy in patients who survived the first year after heart transplantation?
In heart transplant recipients, statin therapy is associated with a significantly reduced risk of developing malignancies and improved overall survival.
Answers are grounded in this paper and cite their sources.
May support statin consideration post-heart transplant for malignancy risk; hypothesis-generating and requires randomized confirmation before practice change.
Background—Although newer immunosuppressive agents, such as mTOR (mammalian target of rapamycin) inhibitors, have lowered the occurrence of malignancies after transplantation, cancer is still a leading cause of death late after heart transplantation. Statins may have an impact on clinical outcomes beyond their lipid-lowering effects. The aim of the present study was to delineate whether statin therapy has an impact on cancer risk and total mortality after heart transplantation.Methods and Results—A total of 255 patients who underwent heart transplantation at the University Hospital Zurich between 1985 and 2007 and survived the first year were included in the present study. The primary outcome measure was the occurrence of any malignancy; the secondary end point was overall survival. During follow-up, a malignancy was diagnosed in 108 patients (42%). The cumulative incidence of tumors 8 years after transplantation was reduced in patients receiving a statin (34% versus 13%; 95% confidence interval, 0.25–0.43 versus 0.07–0.18;P<0.003). Statin use was associated with improved cancer-free and overall survival (bothP<0.0001). A Cox regression model that analyzed the time to tumor formation with or without statin therapy, adjusted for age, male sex, type of cardiomyopathy, and immunosuppressive therapy (including switch to mTOR inhibitors or tacrolimus), demonstrated a superior survival in the statin group. Statins reduced the hazard of occurrence of any malignancy by 67% (hazard ratio, 0.33; 95% confidence interval, 0.21–0.51;P<0.0001).Conclusions—Although it is not possible to adjust for all potential confounders because of the very long follow-up period, this registry suggests that statin use is associated with improved cancer-free and overall survival after cardiac transplantation. These data will need to be confirmed in a prospective trial.
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Fröhlich et al. (2012) conducted a cohort in Heart transplantation (n=255). Statin therapy vs. No statin therapy was evaluated on Occurrence of any malignancy (HR 0.33, 95% CI 0.21-0.51, p=<0.0001). Statin use after heart transplantation was associated with a 67% reduction in the hazard of any malignancy (HR 0.33; 95% CI 0.21-0.51; P<0.0001) and improved cancer-free and overall survival.
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