The impact of rituximab in ABO-incompatible pediatric living donor liver transplantation: the experience of a single center

Pediatr Transplant. 2015 May;19(3):279-86. doi: 10.1111/petr.12445. Epub 2015 Feb 18.

Abstract

Previous studies have demonstrated the safety of ABO-incompatible pediatric LDLT using preoperative plasmapheresis and rituximab; however, no reports have described the timing and dosage of rituximab administration for pediatric LDLT. This study aimed to describe a safe and effective dosage and timing of rituximab for patients undergoing pediatric ABO-incompatible LDLT based on the experience of our single center. A total of 192 LDLTs in 187 patients were examined. These cases included 29 ABO-incompatible LDLTs in 28 patients. Rituximab was used beginning in January 2004 in recipients older than two yr of age (first period: 375 mg/m(2) in two cases; second period: 50 mg/m(2) in two cases; and 200 mg/m(2) in eight cases). Two patients who received 375 mg/m(2) rituximab died of Pneumocystis carinii pneumonia and hemophagocytic syndrome. One patient who received 50 mg/m(2) rituximab required retransplantation as a consequence of antibody-mediated complications. All eight patients administered 200 mg/m(2) survived, and the mean CD20(+) lymphocyte count was 0.1% at the time of LDLT. In the preoperative management of patients undergoing pediatric ABO-incompatible LDLT, the administration of 200 mg/m(2) rituximab three wk prior to LDLT was safe and effective.

Keywords: ABO-incompatibility; living donor liver transplantation; pediatric transplantation; rituximab.

MeSH terms

  • ABO Blood-Group System / immunology*
  • Blood Group Incompatibility / immunology*
  • Child
  • Child, Preschool
  • Female
  • Graft Survival
  • Humans
  • Immunosuppressive Agents / therapeutic use*
  • Infant
  • Liver Failure / surgery
  • Liver Transplantation / methods*
  • Living Donors
  • Lymphohistiocytosis, Hemophagocytic / diagnosis
  • Male
  • Plasmapheresis
  • Pneumonia, Pneumocystis / diagnosis
  • Postoperative Period
  • Reoperation
  • Rituximab / therapeutic use*
  • Time Factors
  • Treatment Outcome

Substances

  • ABO Blood-Group System
  • Immunosuppressive Agents
  • Rituximab