Daratumumab for Delayed Red-Cell Engraftment after Allogeneic Transplantation
Author(s) -
Claudia I. Chapuy,
Richard M. Kaufman,
Edwin P. Alyea,
Jean M. Connors
Publication year - 2018
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa1807438
Subject(s) - daratumumab , medicine , pure red cell aplasia , abo blood group system , transplantation , multiple myeloma , immunology , antibody , monoclonal antibody , bone marrow
Daratumumab, a human IgG1κ monoclonal antibody targeting CD38, is used to treat multiple myeloma. We describe successful treatment with daratumumab in a case of treatment-refractory pure red-cell aplasia after ABO-mismatched allogeneic stem-cell transplantation. The patient was a 72-year-old man with the myelodysplastic syndrome who received a transplant from an HLA-matched, unrelated donor with a major ABO incompatibility (blood group A in the donor and blood group O in the recipient). The patient had persistent circulating anti-A antibodies and no red-cell recovery 200 days after transplantation. Standard treatments had no effect. Within 1 week after the initiation of treatment with daratumumab, he no longer required transfusions.
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