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Tytuł pozycji:

Optimizing transfusion management of multiple myeloma patients receiving daratumumab-based regimens.

Tytuł:
Optimizing transfusion management of multiple myeloma patients receiving daratumumab-based regimens.
Autorzy:
Phou S; Department of Pathology, University of California San Diego, La Jolla, California, USA.
Costello C; Division of Blood and Marrow Transplantation, University of California San Diego, La Jolla, California, USA.
Kopko PM; Department of Pathology, University of California San Diego, La Jolla, California, USA.
Allen ES; Department of Pathology, University of California San Diego, La Jolla, California, USA.
Źródło:
Transfusion [Transfusion] 2021 Jul; Vol. 61 (7), pp. 2054-2063. Date of Electronic Publication: 2021 May 07.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Original Publication: Arlington, Va. : American Association Of Blood Banks
MeSH Terms:
Artifacts*
Blood Grouping and Crossmatching*/methods
Blood Transfusion*
Antibodies, Monoclonal/*immunology
Antineoplastic Agents, Immunological/*immunology
Antineoplastic Combined Chemotherapy Protocols/*therapeutic use
Blood Group Incompatibility/*blood
Erythrocytes/*immunology
Isoantibodies/*blood
Multiple Myeloma/*therapy
Adult ; Aged ; Aged, 80 and over ; Allografts ; Antibodies, Monoclonal/administration & dosage ; Antibodies, Monoclonal/therapeutic use ; Antineoplastic Agents, Immunological/administration & dosage ; Antineoplastic Agents, Immunological/therapeutic use ; Blood Group Antigens/immunology ; Blood Group Incompatibility/diagnosis ; Blood Group Incompatibility/epidemiology ; Combined Modality Therapy ; Dithiothreitol/pharmacology ; Erythrocytes/drug effects ; Female ; Hematopoietic Stem Cell Transplantation ; Humans ; Incidence ; Isoantibodies/biosynthesis ; Isoantibodies/immunology ; Male ; Middle Aged ; Multiple Myeloma/drug therapy ; Transplantation, Autologous
References:
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Quach H, Benson S, Haysom H, Wilkes AM, Zacher N, Cole-Sinclair M, et al. Considerations for pre-transfusion immunohaematology testing in patients receiving the anti-CD38 monoclonal antibody daratumumab for the treatment of multiple myeloma. Intern Med J. 2018;48:210-20.
Chapuy CI, Nicholson RT, Aguad MD, Chapuy B, Laubach JP, Richardson PG, et al. Resolving the daratumumab interference with blood compatibility testing. Transfusion. 2015;55:1545-54.
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Karafin MS, Westlake M, Hauser RG, Tormey CA, Norris PJ, Roubinian NH, et al. Risk factors for red blood cell alloimmunization in the recipient epidemiology and donor evaluation study (REDS-III) database. Br J Haematol. 2018;181:672-81.
Chapuy CI, Aguad MD, Nicholson RT, AuBuchon JP, Cohn CS, Delaney M, et al. International validation of a dithiothreitol (DTT)-based method to resolve the daratumumab interference with blood compatibility testing. Transfusion. 2016;56:2964-72.
Cushing MM, DeSimone RA, Goel R, Hsu YS, Parra P, Racine-Brzostek SE, et al. The impact of daratumumab on transfusion service costs. Transfusion. 2019;59:1252-8.
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Grant Information:
University of California
Contributed Indexing:
Keywords: immunohematology (RBC serology, blood groups); transfusion practices (Oncology-Hematology); transfusion service operations
Substance Nomenclature:
0 (Antibodies, Monoclonal)
0 (Antineoplastic Agents, Immunological)
0 (Blood Group Antigens)
0 (Isoantibodies)
4Z63YK6E0E (daratumumab)
T8ID5YZU6Y (Dithiothreitol)
Entry Date(s):
Date Created: 20210507 Date Completed: 20210813 Latest Revision: 20210813
Update Code:
20240104
DOI:
10.1111/trf.16425
PMID:
33960433
Czasopismo naukowe
Background: Daratumumab, a human anti-CD38 monoclonal antibody used to treat multiple myeloma, interferes with pretransfusion testing and can mask alloantibodies. Incidence of alloimmunization in patients on daratumumab has not been well characterized, and optimal transfusion guidelines regarding prophylactic antigen matching, accounting for both patient safety and efficiency, have not been well established for these patients.
Methods: Records of patients who received daratumumab between January 1, 2014 and July 2, 2019 were reviewed. Daratumumab interference with pretransfusion testing was managed by testing with reagent red blood cells (RBCs) treated with 0.2 M dithiothreitol. When daratumumab was present during antibody testing, patients were transfused with RBC units prophylactically matched for D, C, c, E, e, and K antigens per hospital policy.
Results: Out of 90 patients identified, 52 received a total of 638 RBC transfusions (average of 12.3 units per patient, SD 17.2, range 1-105, median 5 among those transfused). Alloantibodies existing before daratumumab initiation were identified in seven patients. No new alloantibodies were detected in any patients after starting daratumumab treatment.
Conclusions: The incidence of alloimmunization in patients receiving daratumumab is low. Whether this is due to the effect of daratumumab, underlying pathophysiology, or other factors, is unknown. Because these patients require a large number of RBC transfusions overall and have little observed alloimmunization, phenotype matching (beyond RhD) may be unnecessary. Since the use of dithiothreitol cannot rule out the presence of anti-K, we recommend transfusion of ABO-compatible units, prophylactically matched for the D and K antigens only.
(© 2021 AABB.)

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