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A novel allogeneic off-the-shelf dendritic cell vaccine for post-remission treatment of elderly patients with acute myeloid leukemia

In elderly acute myeloid leukemia (AML) patients post-remission treatment options are associated with high comorbidity rates and poor survival. Dendritic cell (DC)-based immunotherapy is a promising alternative treatment strategy. A novel allogeneic DC vaccine, DCP-001, was developed from an AML-der...

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Autores principales: van de Loosdrecht, Arjan A., van Wetering, Sandra, Santegoets, Saskia J. A. M., Singh, Satwinder Kaur, Eeltink, Corien M., den Hartog, Yvonne, Koppes, Malika, Kaspers, Jorn, Ossenkoppele, Gert J., Kruisbeek, Ada M., de Gruijl, Tanja D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182404/
https://www.ncbi.nlm.nih.gov/pubmed/30039426
http://dx.doi.org/10.1007/s00262-018-2198-9
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author van de Loosdrecht, Arjan A.
van Wetering, Sandra
Santegoets, Saskia J. A. M.
Singh, Satwinder Kaur
Eeltink, Corien M.
den Hartog, Yvonne
Koppes, Malika
Kaspers, Jorn
Ossenkoppele, Gert J.
Kruisbeek, Ada M.
de Gruijl, Tanja D.
author_facet van de Loosdrecht, Arjan A.
van Wetering, Sandra
Santegoets, Saskia J. A. M.
Singh, Satwinder Kaur
Eeltink, Corien M.
den Hartog, Yvonne
Koppes, Malika
Kaspers, Jorn
Ossenkoppele, Gert J.
Kruisbeek, Ada M.
de Gruijl, Tanja D.
author_sort van de Loosdrecht, Arjan A.
collection PubMed
description In elderly acute myeloid leukemia (AML) patients post-remission treatment options are associated with high comorbidity rates and poor survival. Dendritic cell (DC)-based immunotherapy is a promising alternative treatment strategy. A novel allogeneic DC vaccine, DCP-001, was developed from an AML-derived cell line that uniquely combines the positive features of allogeneic DC vaccines and expression of multi-leukemia-associated antigens. Here, we present data from a phase I study conducted with DCP-001 in 12 advanced-stage elderly AML patients. Patients enrolled were in complete remission (CR1/CR2) (n = 5) or had smoldering disease (n = 7). All patients were at high risk of relapse and ineligible for post-remission intensification therapies. A standard 3 + 3 dose escalation design with extension to six patients in the highest dose was performed. Patients received four biweekly intradermal DCP-001 injections at different dose levels (10, 25, and 50 million cells DCP-001) and were monitored for clinical and immunological responses. Primary objectives of the study (feasibility and safety) were achieved with 10/12 patients completing the vaccination program. Treatment was well tolerated. A clear-cut distinction between patients with and without detectable circulating leukemic blasts during the vaccination period was noted. Patients with no circulating blasts showed an unusually prolonged survival [median overall survival 36 months (range 7–63) from the start of vaccination] whereas patients with circulating blasts, died within 6 months. Long-term survival was correlated with maintained T cell levels and induction of multi-functional immune responses. It is concluded that DCP-001 in elderly AML patients is safe, feasible and generates both cellular and humoral immune responses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00262-018-2198-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-61824042018-10-22 A novel allogeneic off-the-shelf dendritic cell vaccine for post-remission treatment of elderly patients with acute myeloid leukemia van de Loosdrecht, Arjan A. van Wetering, Sandra Santegoets, Saskia J. A. M. Singh, Satwinder Kaur Eeltink, Corien M. den Hartog, Yvonne Koppes, Malika Kaspers, Jorn Ossenkoppele, Gert J. Kruisbeek, Ada M. de Gruijl, Tanja D. Cancer Immunol Immunother Original Article In elderly acute myeloid leukemia (AML) patients post-remission treatment options are associated with high comorbidity rates and poor survival. Dendritic cell (DC)-based immunotherapy is a promising alternative treatment strategy. A novel allogeneic DC vaccine, DCP-001, was developed from an AML-derived cell line that uniquely combines the positive features of allogeneic DC vaccines and expression of multi-leukemia-associated antigens. Here, we present data from a phase I study conducted with DCP-001 in 12 advanced-stage elderly AML patients. Patients enrolled were in complete remission (CR1/CR2) (n = 5) or had smoldering disease (n = 7). All patients were at high risk of relapse and ineligible for post-remission intensification therapies. A standard 3 + 3 dose escalation design with extension to six patients in the highest dose was performed. Patients received four biweekly intradermal DCP-001 injections at different dose levels (10, 25, and 50 million cells DCP-001) and were monitored for clinical and immunological responses. Primary objectives of the study (feasibility and safety) were achieved with 10/12 patients completing the vaccination program. Treatment was well tolerated. A clear-cut distinction between patients with and without detectable circulating leukemic blasts during the vaccination period was noted. Patients with no circulating blasts showed an unusually prolonged survival [median overall survival 36 months (range 7–63) from the start of vaccination] whereas patients with circulating blasts, died within 6 months. Long-term survival was correlated with maintained T cell levels and induction of multi-functional immune responses. It is concluded that DCP-001 in elderly AML patients is safe, feasible and generates both cellular and humoral immune responses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00262-018-2198-9) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-07-23 2018 /pmc/articles/PMC6182404/ /pubmed/30039426 http://dx.doi.org/10.1007/s00262-018-2198-9 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
van de Loosdrecht, Arjan A.
van Wetering, Sandra
Santegoets, Saskia J. A. M.
Singh, Satwinder Kaur
Eeltink, Corien M.
den Hartog, Yvonne
Koppes, Malika
Kaspers, Jorn
Ossenkoppele, Gert J.
Kruisbeek, Ada M.
de Gruijl, Tanja D.
A novel allogeneic off-the-shelf dendritic cell vaccine for post-remission treatment of elderly patients with acute myeloid leukemia
title A novel allogeneic off-the-shelf dendritic cell vaccine for post-remission treatment of elderly patients with acute myeloid leukemia
title_full A novel allogeneic off-the-shelf dendritic cell vaccine for post-remission treatment of elderly patients with acute myeloid leukemia
title_fullStr A novel allogeneic off-the-shelf dendritic cell vaccine for post-remission treatment of elderly patients with acute myeloid leukemia
title_full_unstemmed A novel allogeneic off-the-shelf dendritic cell vaccine for post-remission treatment of elderly patients with acute myeloid leukemia
title_short A novel allogeneic off-the-shelf dendritic cell vaccine for post-remission treatment of elderly patients with acute myeloid leukemia
title_sort novel allogeneic off-the-shelf dendritic cell vaccine for post-remission treatment of elderly patients with acute myeloid leukemia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182404/
https://www.ncbi.nlm.nih.gov/pubmed/30039426
http://dx.doi.org/10.1007/s00262-018-2198-9
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