Seminars in Pediatric Surgery
Volume 15, Issue 3 , Pages 179-187, August 2006

Malignancy in pediatric transplant recipients

  • Joseph F. Buell, MD

      Affiliations

    • The Israel Penn International Transplant Tumor Registry, Division of Transplantation, University of Cincinnati, Cincinnati, Ohio
    • Corresponding Author InformationAddress reprint requests and correspondence: Joseph F. Buell, MD, University of Cincinnati, The Israel Penn International Tranpslant Tumor Registry, Division of Transplantation, 231 Albert Sabin Way, Cincinnati, OH 45267.
  • ,
  • Thomas G. Gross, MD, PhD

      Affiliations

    • Division of Pediatric Hematology Oncology, Columbus Children’s Hospital, Columbus, Ohio
  • ,
  • Mark J. Thomas, MD

      Affiliations

    • The Israel Penn International Transplant Tumor Registry, Division of Transplantation, University of Cincinnati, Cincinnati, Ohio
  • ,
  • Guy Neff, MD

      Affiliations

    • The Israel Penn International Transplant Tumor Registry, Division of Transplantation, University of Cincinnati, Cincinnati, Ohio
  • ,
  • Chandar Muthiah

      Affiliations

    • The Israel Penn International Transplant Tumor Registry, Division of Transplantation, University of Cincinnati, Cincinnati, Ohio
  • ,
  • Rita Alloway, PharmD

      Affiliations

    • The Israel Penn International Transplant Tumor Registry, Division of Transplantation, University of Cincinnati, Cincinnati, Ohio
  • ,
  • Frederick C. Ryckman, MD

      Affiliations

    • Division of Pediatric Surgery, Cincinnati’s Children’s Hospital, Cincinnati, Ohio.
  • ,
  • Gregory M. Tiao, MD

      Affiliations

    • The Israel Penn International Transplant Tumor Registry, Division of Transplantation, University of Cincinnati, Cincinnati, Ohio
  • ,
  • E. Steve Woodle, MD

      Affiliations

    • The Israel Penn International Transplant Tumor Registry, Division of Transplantation, University of Cincinnati, Cincinnati, Ohio

Malignancy is a well defined complication of chronic immunosuppression. Post transplant malignancies appear to be related to cumulative doses of immunosuppression, and in pediatric patients, acute infection of previously naive patients. The most commonly encountered malignancy in this age population is Post Transplant Lymphoproliferative Disorder (PTLD). PTLD is not a single entity but rather represents a continuum of disease. Treatment of PTLD should be initiated with immunosuppression reduction. Standard dose chemotherapy leads to significant morbidity. With the introduction of anti-CD20 antibody treatment with rituximab, chemotherapy has become second line therapy. The occurrence of solid malignancy appears to be associated with chronic immunosuppression. These cancers include those of skin, gynecologic organs, and the rectum, all of which appear to have the strongest association with viral mediators. Several strategies have been postulated to minimize the occurrence of malignancy. These include ganciclovir prophylaxis for the prevention of PTLD and the use of mychophenolic acid and TOR inhibitor maintenance to diminish the incidence of PTLD and solid malignancies. This leaves transplant physicians with several new and novel immunosuppressive agents with uncertain oncologic potentials that will need to be examined over the next decade.

Index words:  Pediatric solid organ transplantation , Chronic immunosuppression , Malignancy in transplant recipients , Lymphoproliferative disorder , Epstein–Barr virus , Viral inducement

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PII: S1055-8586(06)00029-1

doi:10.1053/j.sempedsurg.2006.03.005

Seminars in Pediatric Surgery
Volume 15, Issue 3 , Pages 179-187, August 2006