Post-transplant lymphoproliferative disorders in children: The role of chemotherapy in the era of rituximab

S. Gallego*, A. Llort, L. Gros, J. Sanchez De Toledo, J. Bueno, A. Moreno, J. Nieto, J. Sanchez De Toledo

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

26 Citations (Scopus)


PTLD are the most frequent neoplasms in children postorgan transplantation. We describe our experience in the treatment of 14 children (three with early and 11 with late-onset disease) treated with a step-wise protocol developed at our institution. Treatment consisted of reducing immunosuppressants, followed by rituximab and chemotherapy if required. Rituximab, incorporated into the protocol in 2001, has been determinant for the total chemotherapy burden patients need to achieve remission. In seven patients who did not receive rituximab, anthracycline total dose ranged from 160 to 240 mg/m2, while only one of the patients receiving rituximab required DOXO (range: 0-120 mg/m2) (p = 0.003). The use of alkylating agents was also notably lower in patients receiving rituximab (median dose = 1200 mg/m2) compared with those who did not receive rituximab (median dose = 5800 mg/m 2) (p = 0.006). Twelve patients are in remission and two died, one from refractory disease and the other from septic shock. Two-year OS and EFS were 85.7% and 57%, respectively. In conclusion, our experience with the use of rituximab in children with PTLD after solid organ transplantation appeared to be associated with a lesser requirement for alkylating agents and anthracyclines compared with historical subjects, suggesting a reduction in the side effects of these agents.

Original languageAmerican English
Pages (from-to)61-66
Number of pages6
JournalPediatric Transplantation
Issue number1
Publication statusPublished - Feb 2010


  • Chemotherapy
  • Children
  • Post-transplant lymphoproliferative disorders
  • Rituximab


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