Renal Transplant Outcomes in Plasma Cell Dyscrasias and AL Amyloidosis after Treatment with Daratumumab

Author:

Mohidin Barian1,Needleman Amy1,Fernando Raymond2,Lowe David M.3ORCID,Wechalekar Ashutosh4,Sheaff Michael5,Salama Alan1,Jones Gareth1

Affiliation:

1. UCL Department of Renal Medicine, Royal Free Hospital, London NW3 2QG, UK

2. H&I Laboratory, Royal Free Hospital, London NW3 2QG, UK

3. UCL Institute of Immunity & Transplantation, Royal Free Hospital, London NW3 2QG, UK

4. Department of Haematology, Royal Free Hospital, London NW3 2QG, UK

5. Department of Cellular Pathology, Royal London Hospital, London NW3 2QG, UK

Abstract

Background: The morbidity and mortality from AL amyloidosis has significantly improved with the development of novel treatments. Daratumumab is a highly effective treatment for AL amyloidosis, but end-stage kidney disease is a common complication of this condition. Kidney transplantation is the ideal form of renal replacement therapy but has historically been contraindicated in this group of patients. Methods: Given the improved survival and better treatments of both conditions, we argue that it is time to reconsider transplanting these patients. Results: We report our experience of transplanting four patients with AL amyloidosis who had achieved stable remission through treatment with daratumumab. Conclusions: We highlight the key challenges involved and discuss important clinical issues for patients receiving daratumumab, particularly the difficulties with interpreting the crossmatch in light of daratumumab and immunoglobulin therapy interference. We also discuss the complexities involved in balancing the risks of infection, relapse, rejection, and immunosuppression in such patients.

Publisher

MDPI AG

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