Abstract
Consecutive patients who presented with biopsy-proven AMR and donor-specific anti-HLA antibodies (DSA) at a single institution between July 2011 and February 2015 were included. They received rituximab 375mg/m<sup>2</sup> on day1, bortezomib 1.3mg/m<sup>2</sup> and methylprednisolone on days 1, 4, 8, 11, and plasmapheresis on days -1, 4, 8, 11, 14, 15, 17, with herpes zoster prophylaxis. The primary outcome was graft survival independent of dialysis. Patients were prospectively assessed with serial monitoring of renal function and proteinuria, and neuropathy symptoms. Toxicity determination was made by medical record review for hospitalizations within 3months of therapy, or documentation of opportunistic infection. Eleven patients were treated for late AMR (diagnosed at a median of 38months post renal transplant) with this bortezomib-based protocol; 2 patients underwent the regimen twice. Of the 11patients, 9 have functioning allografts (82% graft survival) with a median creatinine of 2.1mg/dL (range 1.1-3.4mg/dL), at a median follow-up of 50months after AMR therapy (range 24-63months). One patient was re-transplanted at 4years post AMR treatment with no AMR recurrence to date at 2-years' follow-up, and a second patient re-initiated dialysis at 2years post AMR treatment. Patient survival is 91% (10/11): 1 patient relocated out of state and was reported to have died from complications of hypertensive encephalopathy. The majority of patients (7/11) had several class I and classII DSA specificities; of these, 4 patients had negative classI DSA but persistent classII DSAs at 2-3 months post therapy. Only 1 patient who was positive for classII DSAs alone (DR53 and DQ2) converted to negative DSA, although DSA testing was delayed to 2years' follow-up. Two patients were hospitalized within 1 month of the protocol, 1 for ileus and 1 for urinary tract infection and ruptured ovarian cyst. One other patient had herpes zoster. Renal allograft survival was 82% at 4years after bortezomib-based therapy for late onset AMR; toxicity profile of this regimen was acceptable. Eradication of DSAs may not be necessary for meaningful and durable renal response. .
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