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Infection Risk Associated with Daratumumab

BACKGROUND: Daratumumab is an IgG kappa monoclonal antibody (mAB) against CD38 which is expressed on myeloma cells. It has recently been approved for treatment of patients with relapsed refractory multiple myeloma. Our objective was to identify the potential infectious complications associated with...

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Autores principales: Johnsrud, Joyce J, Susanibar, Sandra, Jo-Kamimoto, Jorge, Johnsrud, Andrew J, Kothari, Atul, Burgess, Mary J, Schinke, Carolina, Thanendrarajan, Sharmilan, Zangari, Maurizio, Davies, Faith, Morgan, Gareth, Vanrhee, Frits, Crescencio, Juan Carlos Rico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630755/
http://dx.doi.org/10.1093/ofid/ofx163.1884
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author Johnsrud, Joyce J
Susanibar, Sandra
Jo-Kamimoto, Jorge
Johnsrud, Andrew J
Kothari, Atul
Burgess, Mary J
Schinke, Carolina
Thanendrarajan, Sharmilan
Zangari, Maurizio
Davies, Faith
Morgan, Gareth
Vanrhee, Frits
Crescencio, Juan Carlos Rico
author_facet Johnsrud, Joyce J
Susanibar, Sandra
Jo-Kamimoto, Jorge
Johnsrud, Andrew J
Kothari, Atul
Burgess, Mary J
Schinke, Carolina
Thanendrarajan, Sharmilan
Zangari, Maurizio
Davies, Faith
Morgan, Gareth
Vanrhee, Frits
Crescencio, Juan Carlos Rico
author_sort Johnsrud, Joyce J
collection PubMed
description BACKGROUND: Daratumumab is an IgG kappa monoclonal antibody (mAB) against CD38 which is expressed on myeloma cells. It has recently been approved for treatment of patients with relapsed refractory multiple myeloma. Our objective was to identify the potential infectious complications associated with daratumumab use. METHODS: We conducted a retrospective analysis of myeloma patients who received daratumumab at our institution from October 2015 to December 2016. Patients were divided into four groups based on administration regimen of daratumumab: (1) single agent with dexamethasone; (2) triple therapy with proteasome inhibitor (PI), immune-modulating drug (IMiD), mitogen-activated protein kinase (MEK) inhibitor or mAB; (3) quadruple therapy with IMiD + PI ± mAB or cyclophosphamide; (4) with high-dose chemotherapy. For each group, we evaluated the incidence of infection, neutropenia (defined as ANC <1,000), hospitalization, and 90-day survival. RESULTS: A total of 171 patients (63% male, 37% female) were included in the study and received a total of 343 cycles of daratumumab. Median age was 68 years. A total of 151 infections occurred in 121 of the 343 cycles (40% bacterial; 52% viral). There was a significant association between development of infection and chemotherapy regimen used (χ(2) = 17, P ≤ 0.001). Patients developed neutropenia in 129 of 254 cycles (51%). There was a significant association between the development of neutropenia and chemotherapy regimen used (χ(2) = 43.51, P < 0.00001). Discontinuation of chemotherapy occurred in 65 cycles (19%), mainly due to progression of disease (54%). Eighty subjects (23%) required hospitalization, infection being the main cause (51%). Ninety-day survival was 91.8%. CONCLUSION: Infection is common among myeloma patients who receive daratumumab. Myeloma patients who receive daratumumab in conjunction with multidrug chemotherapy regimens have an increased risk of infection and neutropenia. Because daratumumab is given predominantly as outpatient therapy, a greater understanding of the potential immunomodulatory effects of daratumumab will lead to increased vigilance in identifying and treating clinically significant infections. DISCLOSURES: F. Davies, Janssen: Consultant, Speaker honorarium. G. Morgan, Janssen: Consultant and Research Contractor, Research support and Speaker honorarium.
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spelling pubmed-56307552017-11-07 Infection Risk Associated with Daratumumab Johnsrud, Joyce J Susanibar, Sandra Jo-Kamimoto, Jorge Johnsrud, Andrew J Kothari, Atul Burgess, Mary J Schinke, Carolina Thanendrarajan, Sharmilan Zangari, Maurizio Davies, Faith Morgan, Gareth Vanrhee, Frits Crescencio, Juan Carlos Rico Open Forum Infect Dis Abstracts BACKGROUND: Daratumumab is an IgG kappa monoclonal antibody (mAB) against CD38 which is expressed on myeloma cells. It has recently been approved for treatment of patients with relapsed refractory multiple myeloma. Our objective was to identify the potential infectious complications associated with daratumumab use. METHODS: We conducted a retrospective analysis of myeloma patients who received daratumumab at our institution from October 2015 to December 2016. Patients were divided into four groups based on administration regimen of daratumumab: (1) single agent with dexamethasone; (2) triple therapy with proteasome inhibitor (PI), immune-modulating drug (IMiD), mitogen-activated protein kinase (MEK) inhibitor or mAB; (3) quadruple therapy with IMiD + PI ± mAB or cyclophosphamide; (4) with high-dose chemotherapy. For each group, we evaluated the incidence of infection, neutropenia (defined as ANC <1,000), hospitalization, and 90-day survival. RESULTS: A total of 171 patients (63% male, 37% female) were included in the study and received a total of 343 cycles of daratumumab. Median age was 68 years. A total of 151 infections occurred in 121 of the 343 cycles (40% bacterial; 52% viral). There was a significant association between development of infection and chemotherapy regimen used (χ(2) = 17, P ≤ 0.001). Patients developed neutropenia in 129 of 254 cycles (51%). There was a significant association between the development of neutropenia and chemotherapy regimen used (χ(2) = 43.51, P < 0.00001). Discontinuation of chemotherapy occurred in 65 cycles (19%), mainly due to progression of disease (54%). Eighty subjects (23%) required hospitalization, infection being the main cause (51%). Ninety-day survival was 91.8%. CONCLUSION: Infection is common among myeloma patients who receive daratumumab. Myeloma patients who receive daratumumab in conjunction with multidrug chemotherapy regimens have an increased risk of infection and neutropenia. Because daratumumab is given predominantly as outpatient therapy, a greater understanding of the potential immunomodulatory effects of daratumumab will lead to increased vigilance in identifying and treating clinically significant infections. DISCLOSURES: F. Davies, Janssen: Consultant, Speaker honorarium. G. Morgan, Janssen: Consultant and Research Contractor, Research support and Speaker honorarium. Oxford University Press 2017-10-04 /pmc/articles/PMC5630755/ http://dx.doi.org/10.1093/ofid/ofx163.1884 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Johnsrud, Joyce J
Susanibar, Sandra
Jo-Kamimoto, Jorge
Johnsrud, Andrew J
Kothari, Atul
Burgess, Mary J
Schinke, Carolina
Thanendrarajan, Sharmilan
Zangari, Maurizio
Davies, Faith
Morgan, Gareth
Vanrhee, Frits
Crescencio, Juan Carlos Rico
Infection Risk Associated with Daratumumab
title Infection Risk Associated with Daratumumab
title_full Infection Risk Associated with Daratumumab
title_fullStr Infection Risk Associated with Daratumumab
title_full_unstemmed Infection Risk Associated with Daratumumab
title_short Infection Risk Associated with Daratumumab
title_sort infection risk associated with daratumumab
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630755/
http://dx.doi.org/10.1093/ofid/ofx163.1884
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