Literature DB >> 22489700

Efficacy and safety of Id-protein-loaded dendritic cell vaccine in patients with multiple myeloma--phase II study results.

L Zahradova1, K Mollova, D Ocadlikova, L Kovarova, Z Adam, M Krejci, L Pour, A Krivanova, V Sandecka, R Hajek.   

Abstract

UNLABELLED: In a phase II clinical study, pretreated multiple myeloma patients with relapsing or stable disease received autologous anticancer vaccine containing dendritic cells loaded with Id-protein. Patients received a total of 6 vaccine doses intradermally in monthly intervals. No clinical responses were observed. During the follow-up with a median of 33.1 months (range: 11-43 months), the disease remained stable in 7/11 (64%) of patients. Immune responses measured by ELISpot were noted in 3/11 (27%) and DTH skin test for Id-protein was positive in 8/11 (73%) of patients; out of those, 1/11 (9%) and 5/11 (46%), respectively, had preexisting immune response to Id-protein before the vaccination began. Outcomes were compared to those of a control group of 13 patients. A trend to lower cumulative incidence of progression in the vaccinated group was observed at 12 months from the first vaccination (p= 0.099). More patients from the control group compared to vaccinated patients required active anticancer therapy [4/11 (36%) vs. 8/13 (62%)]. Vaccines based on dendritic cells loaded with Id-protein are safe and induce specific immune response in multiple myeloma patients. Our results suggest that the vaccination could stabilize the disease in approximately two-thirds of patients. KEYWORDS: dendritic cells, immunotherapy, anticancer vaccines, Id-protein, multiple myeloma.

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Year:  2012        PMID: 22489700     DOI: 10.4149/neo_2012_057

Source DB:  PubMed          Journal:  Neoplasma        ISSN: 0028-2685            Impact factor:   2.575


  10 in total

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2.  Mouse dendritic cell migration in abdominal lymph nodes by intraperitoneal administration.

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3.  Identification of human leucocyte antigen (HLA)-A*0201-restricted cytotoxic T lymphocyte epitopes derived from HLA-DOβ as a novel target for multiple myeloma.

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9.  Compromised functionality of monocyte-derived dendritic cells in multiple myeloma patients may limit their use in cancer immunotherapy.

Authors:  Prajakta Shinde; Sophia Fernandes; Sameer Melinkeri; Vaijayanti Kale; Lalita Limaye
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Review 10.  Dendritic Cell-Based Immunotherapy in Multiple Myeloma: Challenges, Opportunities, and Future Directions.

Authors:  Emma Verheye; Jesús Bravo Melgar; Sofie Deschoemaeker; Geert Raes; Anke Maes; Elke De Bruyne; Eline Menu; Karin Vanderkerken; Damya Laoui; Kim De Veirman
Journal:  Int J Mol Sci       Date:  2022-01-14       Impact factor: 5.923

  10 in total

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