Efficacy, Outcomes, and Cost-Effectiveness of Desensitization Using IVIG and Rituximab
Authors:
- 27 March 2013
- journal article
- research article
- Published by Wolters Kluwer Health in Transplantation
- Vol. 95 (6) , 852-858
Abstract
Background Transplantation rates are very low for the broadly sensitized patient (panel reactive antibody [PRA]>80%; HS). Here, we examine the efficacy, outcomes, and cost-effectiveness of desensitization using high-dose intravenous immunoglobulin (IVIG) and rituximab to improve transplantation rates in HS patients. Methods From July 2006 to December 2011, 207 HS (56 living donors/151 deceased donors) patients (donor-specific antibody positive, PRA>80%) were desensitized using IVIG and rituximab. After desensitization, responsive patients proceeded to transplantation with an acceptable crossmatch. Cost and outcomes of desensitization were compared with dialysis. Results Of the 207 treated patients, 146 (71%) were transplanted. At 48 months, patient and graft survival by Kaplan–Meier were 95% and 87.5%, respectively. The total 3-year cost for patients treated in the desensitization arm was $219,914 per patient compared with $238,667 per patient treated in the dialysis arm. Thus, each patient treated with desensitization is estimated to save the U.S. healthcare system $18,753 in 2011 USD. Overall, estimated patient survival at the end of 3 years was 96.6% for patients in the desensitization arm of the model (based on Cedars-Sinai survival rate) compared with 79.0% for an age, end-stage renal disease etiology, and PRA matched group of patients remaining on dialysis during the study period. Conclusions We conclude that desensitization with IVIG+rituximab is clinically and cost-effective, with both financial savings and an estimated 17.6% greater probability of 3-year survival associated with desensitization versus dialysis alone. However, the benefits of desensitization and transplantation are limited by organ availability and allocation policies.Keywords
This publication has 17 references indexed in Scilit:
- Infectious Complications in Kidney-Transplant Recipients Desensitized with Rituximab and Intravenous ImmunoglobulinClinical Journal of the American Society of Nephrology, 2011
- Understanding the Causes of Kidney Transplant Failure: The Dominant Role of Antibody-Mediated Rejection and NonadherenceAmerican Journal of Transplantation, 2011
- Desensitization in HLA-Incompatible Kidney Recipients and SurvivalNew England Journal of Medicine, 2011
- Use of Intravenous Immune Globulin and Rituximab for Desensitization of Highly Human Leukocyte Antigen-Sensitized Patients Awaiting Kidney TransplantationTransplantation, 2010
- Evidence for Antibody-Mediated Injury as a Major Determinant of Late Kidney Allograft FailureTransplantation, 2010
- Acute Hemolysis After High-Dose Intravenous Immunoglobulin Therapy in Highly HLA Sensitized PatientsClinical Journal of the American Society of Nephrology, 2009
- Antibody-Mediated Microcirculation Injury Is the Major Cause of Late Kidney Transplant FailureAmerican Journal of Transplantation, 2009
- Rituximab and Intravenous Immune Globulin for Desensitization during Renal TransplantationNew England Journal of Medicine, 2008
- Analysis of Subcutaneous (SQ) Alemtuzumab Induction Therapy in Highly Sensitized Patients Desensitized With IVIG and RituximabAmerican Journal of Transplantation, 2008
- Safety and Adverse Events Profiles of Intravenous Gammaglobulin Products Used for ImmunomodulationClinical Journal of the American Society of Nephrology, 2006