Malignancy After Heart Transplantation Under Everolimus Versus Mycophenolate Mofetil Immunosuppression
Adult
Immunosuppression Therapy
Male
Adolescent
Incidence
Lymphoma, Non-Hodgkin
Infant
Kaplan-Meier Estimate
Middle Aged
Mycophenolic Acid
3. Good health
03 medical and health sciences
0302 clinical medicine
Child, Preschool
Animals
Heart Transplantation
Humans
Female
Everolimus
Child
Immunosuppressive Agents
Aged
Follow-Up Studies
DOI:
10.1016/j.transproceed.2015.12.071
Publication Date:
2016-05-24T23:36:42Z
AUTHORS (12)
ABSTRACT
With advances in immunosuppressive therapy, heart transplantation is currently recommended as the only established surgical treatment for refractory heart failure. However, chronic immunosuppression increases the risk for malignancy. Everolimus (EVR) is a potent mammalian target of rapamycin inhibitor that is used after transplantation and to treat advanced malignancies, as we have done in Taiwan after heart transplantation since 2004. Mycophenolate mofetil (MMF) and EVR are frequently used as cell-cycle inhibitors to optimize post-transplantation outcomes.We retrospectively analyzed the characteristics and outcomes of 454 patients who received either MMF (n = 232) or EVR (n = 222) after heart transplantation at the National Taiwan University Hospital from March 1, 1990, to March 1, 2015. Patient characteristics and Kaplan-Meier survival curves were compared between groups.During a median follow-up of 69.2 months, malignancy was diagnosed in 27 patients receiving MMF (n = 23) or EVR (n = 4). There was a significant difference in malignancy risk between groups (9.91% vs 1.80%, P = .001). The most common malignancies were non-Hodgkin lymphoma, skin cancers, and lung squamous cell carcinoma. The 2-year overall survival after malignancy was 50% in the EVR group and 47% in the MMF group (P = .745).EVR treatment after heart transplant is associated with a lower risk of malignancy than is MMF treatment. The 2-year survival rate after malignancy was similar between EVR and MMF groups.
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