Volume 21, Issue 3 e12873
ORIGINAL ARTICLE

Bortezomib in the treatment of antibody-mediated rejection in pediatric kidney transplant recipients: A multicenter Midwest Pediatric Nephrology Consortium study

Sarah Kizilbash

Corresponding Author

Sarah Kizilbash

University of Minnesota, Minneapolis, MN, USA

Correspondence

Sarah Kizilbash, University of Minnesota, Minneapolis, MN, USA.

Email: [email protected]

Search for more papers by this author
Donna Claes

Donna Claes

Cincinnati Children's Hospital, Cincinnati, OH, USA

Search for more papers by this author
Isa Ashoor

Isa Ashoor

Children's Hospital New Orleans, New Orleans, LA, USA

Search for more papers by this author
Ashton Chen

Ashton Chen

Wake Forest School of Medicine, Winston-Salem, NC, USA

Search for more papers by this author
Sara Jandeska

Sara Jandeska

Rush University, Chicago, IL, USA

Search for more papers by this author
Raed Bou Matar

Raed Bou Matar

Cleveland Clinic, Cleveland, OH, USA

Search for more papers by this author
Jason Misurac

Jason Misurac

University of Iowa, Iowa, IA, USA

Search for more papers by this author
Joseph Sherbotie

Joseph Sherbotie

University of Utah, Salt Lake City, UT, USA

Search for more papers by this author
Katherine Twombley

Katherine Twombley

Medical University of South Carolina, Charleston, SC, USA

Search for more papers by this author
Priya Verghese

Priya Verghese

University of Minnesota, Minneapolis, MN, USA

Search for more papers by this author
First published: 16 January 2017
Citations: 24

Abstract

Antibody-mediated rejection leads to allograft loss after kidney transplantation. Bortezomib has been used in adults for the reversal of antibody-mediated rejection; however, pediatric data are limited. This retrospective study was conducted in collaboration with the Midwest Pediatric Nephrology Consortium. Pediatric kidney transplant recipients who received bortezomib for biopsy-proven antibody-mediated rejection between 2008 and 2015 were included. The objective was to characterize the use of bortezomib in pediatric kidney transplant recipients. Thirty-three patients received bortezomib for antibody-mediated rejection at nine pediatric kidney transplant centers. Ninety percent of patients received intravenous immunoglobulin, 78% received plasmapheresis, and 78% received rituximab. After a median follow-up of 15 months, 65% of patients had a functioning graft. The estimated glomerular filtration rate improved or stabilized in 61% and 36% of patients at 3 and 12 months post-bortezomib, respectively. The estimated glomerular filtration rate at diagnosis significantly predicted estimated glomerular filtration rate at 12 months after adjusting for chronic histologic changes (P .001). Fifty-six percent of patients showed an at least 25% reduction in the mean fluorescence intensity of the immune-dominant donor-specific antibody, 1-3 months after the first dose of bortezomib. Non-life-threatening side effects were documented in 21 of 33 patients. Pediatric kidney transplant recipients tolerated bortezomib without life-threatening side effects. Bortezomib may stabilize estimated glomerular filtration rate for 3-6 months in pediatric kidney transplant recipients with antibody-mediated rejection.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.