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Immunostimulatory AdCD40L gene therapy combined with low-dose cyclophosphamide in metastatic melanoma patients

BACKGROUND: Current approaches for treating metastatic malignant melanoma (MM) are not effective enough and are associated with serious adverse events. Due to its immunogenicity, melanoma is an attractive target for immunostimulating therapy. In this phase I/IIa study, local AdCD40L immunostimulator...

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Autores principales: Loskog, Angelica, Maleka, Aglaia, Mangsbo, Sara, Svensson, Emma, Lundberg, Christina, Nilsson, Anders, Krause, Johan, Agnarsdóttir, Margrét, Sundin, Anders, Ahlström, Håkan, Tötterman, Thomas H, Ullenhag, Gustav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4984796/
https://www.ncbi.nlm.nih.gov/pubmed/27031851
http://dx.doi.org/10.1038/bjc.2016.42
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author Loskog, Angelica
Maleka, Aglaia
Mangsbo, Sara
Svensson, Emma
Lundberg, Christina
Nilsson, Anders
Krause, Johan
Agnarsdóttir, Margrét
Sundin, Anders
Ahlström, Håkan
Tötterman, Thomas H
Ullenhag, Gustav
author_facet Loskog, Angelica
Maleka, Aglaia
Mangsbo, Sara
Svensson, Emma
Lundberg, Christina
Nilsson, Anders
Krause, Johan
Agnarsdóttir, Margrét
Sundin, Anders
Ahlström, Håkan
Tötterman, Thomas H
Ullenhag, Gustav
author_sort Loskog, Angelica
collection PubMed
description BACKGROUND: Current approaches for treating metastatic malignant melanoma (MM) are not effective enough and are associated with serious adverse events. Due to its immunogenicity, melanoma is an attractive target for immunostimulating therapy. In this phase I/IIa study, local AdCD40L immunostimulatory gene therapy was evaluated in patients with MM. METHODS: AdCD40L is an adenovirus carrying the gene for CD40 ligand. Patients that failed standard treatments were enrolled. Six patients received four weekly intratumoral AdCD40L injections. Next, nine patients received low-dose cyclophosphamide conditioning before the first and fourth AdCD40L injection. The blood samples were collected at multiple time points for chemistry, haematology and immunology evaluations. Radiology was performed at enrolment and repeated twice after the treatment. RESULTS: AdCD40L was safe with mild transient reactions. No objective responses were recorded by MRI, however, local and distant responses were seen on FDG-PET. The overall survival at 6 months was significantly better when cyclophosphamide was added to AdCD40L. The patients with the best survival developed the highest levels of activated T cells and experienced a pronounced decrease of intratumoral IL8. CONCLUSIONS: AdCD40L therapy for MM was well tolerated. Local and distant responses along with better survival in the low-dose cyclophosphamide group are encouraging.
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spelling pubmed-49847962017-04-12 Immunostimulatory AdCD40L gene therapy combined with low-dose cyclophosphamide in metastatic melanoma patients Loskog, Angelica Maleka, Aglaia Mangsbo, Sara Svensson, Emma Lundberg, Christina Nilsson, Anders Krause, Johan Agnarsdóttir, Margrét Sundin, Anders Ahlström, Håkan Tötterman, Thomas H Ullenhag, Gustav Br J Cancer Clinical Study BACKGROUND: Current approaches for treating metastatic malignant melanoma (MM) are not effective enough and are associated with serious adverse events. Due to its immunogenicity, melanoma is an attractive target for immunostimulating therapy. In this phase I/IIa study, local AdCD40L immunostimulatory gene therapy was evaluated in patients with MM. METHODS: AdCD40L is an adenovirus carrying the gene for CD40 ligand. Patients that failed standard treatments were enrolled. Six patients received four weekly intratumoral AdCD40L injections. Next, nine patients received low-dose cyclophosphamide conditioning before the first and fourth AdCD40L injection. The blood samples were collected at multiple time points for chemistry, haematology and immunology evaluations. Radiology was performed at enrolment and repeated twice after the treatment. RESULTS: AdCD40L was safe with mild transient reactions. No objective responses were recorded by MRI, however, local and distant responses were seen on FDG-PET. The overall survival at 6 months was significantly better when cyclophosphamide was added to AdCD40L. The patients with the best survival developed the highest levels of activated T cells and experienced a pronounced decrease of intratumoral IL8. CONCLUSIONS: AdCD40L therapy for MM was well tolerated. Local and distant responses along with better survival in the low-dose cyclophosphamide group are encouraging. Nature Publishing Group 2016-04-12 2016-03-31 /pmc/articles/PMC4984796/ /pubmed/27031851 http://dx.doi.org/10.1038/bjc.2016.42 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Clinical Study
Loskog, Angelica
Maleka, Aglaia
Mangsbo, Sara
Svensson, Emma
Lundberg, Christina
Nilsson, Anders
Krause, Johan
Agnarsdóttir, Margrét
Sundin, Anders
Ahlström, Håkan
Tötterman, Thomas H
Ullenhag, Gustav
Immunostimulatory AdCD40L gene therapy combined with low-dose cyclophosphamide in metastatic melanoma patients
title Immunostimulatory AdCD40L gene therapy combined with low-dose cyclophosphamide in metastatic melanoma patients
title_full Immunostimulatory AdCD40L gene therapy combined with low-dose cyclophosphamide in metastatic melanoma patients
title_fullStr Immunostimulatory AdCD40L gene therapy combined with low-dose cyclophosphamide in metastatic melanoma patients
title_full_unstemmed Immunostimulatory AdCD40L gene therapy combined with low-dose cyclophosphamide in metastatic melanoma patients
title_short Immunostimulatory AdCD40L gene therapy combined with low-dose cyclophosphamide in metastatic melanoma patients
title_sort immunostimulatory adcd40l gene therapy combined with low-dose cyclophosphamide in metastatic melanoma patients
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4984796/
https://www.ncbi.nlm.nih.gov/pubmed/27031851
http://dx.doi.org/10.1038/bjc.2016.42
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