Heart transplant recipients experience high rates of skin cancer, likely due to greater length or dosage of immunosuppression. We review the impact of immunosuppressive medications on development of nonmelanoma skin cancer (NMSC) in heart transplant recipients. The authors searched keywords "heart transplant" and "nonmelanoma skin cancer" on PubMed in October 2022 for eligible articles available in English. Articles were selected for inclusion based on relevance to heart transplantation and NMSC. If any cited articles within included articles were related to our search they were also included. Of the 29 identified articles, 18 met the inclusion criteria with a total of 11,699 patients. Two studies found that tacrolimus and azathioprine increased the risk of NMSC. Five studies demonstrated that tacrolimus, everolimus, sirolimus, azathioprine and mycophenolate mofetil decreased the risk of NMSC. Three studies described that cyclosporine, tacrolimus, everolimus, sirolimus, azathioprine, mycophenolate mofetil and prednisone had no significant association with the development in NMSC. Two studies did not specify the correlation between immunosuppressant use and NMSC development. Ten studies did not discuss the association of immunosuppressants use with the development of NMSC. Our review highlights the commonly used immunosuppressive drugs that can impact the development of NMSC in heart transplant recipients. A management strategy in immunosuppression-associated skin cancers may ultimately involve adjusting the immunosuppressive regimen. This review serves as a summary of the most commonly used immunosuppressive drugs in heart transplant patients and their tumorigenic mechanisms to guide recommendations for dermatologic follow-up in heart transplant recipients.
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Western Univ Hlth Sci, Pomona, CA USAWestern Univ Hlth Sci, Pomona, CA USA
Cheng, Melissa A.
Mahlberg, Scott J.
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Case Western Reserve Univ, Med Ctr, Univ Hosp Cleveland, Cleveland, OH USAWestern Univ Hlth Sci, Pomona, CA USA
Mahlberg, Scott J.
Hill, Sheena T.
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Case Western Reserve Univ, Med Ctr, Univ Hosp Cleveland, Cleveland, OH USAWestern Univ Hlth Sci, Pomona, CA USA
Hill, Sheena T.
Bordeaux, Jeremy S.
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Univ Hosp Cleveland, Mohs Microg & Dermatol Surg, Med Ctr, Cleveland, OH USA
Case Western Reserve Univ, Cleveland Med Ctr, Med Ctr, Univ Hosp Cleveland,Melanoma Program, Cleveland, OH USAWestern Univ Hlth Sci, Pomona, CA USA
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Kaiser Permanente Los Angeles Med Ctr, Dept Dermatol, Los Angeles, CA USAKaiser Permanente Los Angeles Med Ctr, Dept Dermatol, Los Angeles, CA USA
Rosenthal, Amanda
Juhasz, Margit L. W.
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Kaiser Permanente Los Angeles Med Ctr, Dept Dermatol, Los Angeles, CA USA
Cedars Sinai Med Ctr, Dept Dermatol, Los Angeles, CA USAKaiser Permanente Los Angeles Med Ctr, Dept Dermatol, Los Angeles, CA USA
Juhasz, Margit L. W.
Chang, Crystal
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Kaiser Permanente Bernard J Tyson Sch Med, Pasadena, CA USAKaiser Permanente Los Angeles Med Ctr, Dept Dermatol, Los Angeles, CA USA
Chang, Crystal
Gharavi, Nima M.
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Cedars Sinai Med Ctr, Dept Dermatol, Los Angeles, CA USAKaiser Permanente Los Angeles Med Ctr, Dept Dermatol, Los Angeles, CA USA
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Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Dermatol, Boston, MA 02215 USAHarvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Dermatol, Boston, MA 02215 USA
Marcil, I
Stern, RS
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Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Dermatol, Boston, MA 02215 USAHarvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Dermatol, Boston, MA 02215 USA