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Surgery and adjuvant dendritic cell-based tumour vaccination for patients with relapsed malignant glioma, a feasibility study
Patients with relapsed malignant glioma have a poor prognosis. We developed a strategy of vaccination using autologous mature dendritic cells loaded with autologous tumour homogenate. In total, 12 patients with a median age of 36 years (range: 11–78) were treated. All had relapsing malignant glioma....
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409960/ https://www.ncbi.nlm.nih.gov/pubmed/15477864 http://dx.doi.org/10.1038/sj.bjc.6602195 |
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author | Rutkowski, S De Vleeschouwer, S Kaempgen, E Wolff, J E A Kühl, J Demaerel, P Warmuth-Metz, M Flamen, P Van Calenbergh, F Plets, C Sörensen, N Opitz, A Van Gool, S W |
author_facet | Rutkowski, S De Vleeschouwer, S Kaempgen, E Wolff, J E A Kühl, J Demaerel, P Warmuth-Metz, M Flamen, P Van Calenbergh, F Plets, C Sörensen, N Opitz, A Van Gool, S W |
author_sort | Rutkowski, S |
collection | PubMed |
description | Patients with relapsed malignant glioma have a poor prognosis. We developed a strategy of vaccination using autologous mature dendritic cells loaded with autologous tumour homogenate. In total, 12 patients with a median age of 36 years (range: 11–78) were treated. All had relapsing malignant glioma. After surgery, vaccines were given at weeks 1 and 3, and later every 4 weeks. A median of 5 (range: 2–7) vaccines was given. There were no serious adverse events except in one patient with gross residual tumour prior to vaccination, who repetitively developed vaccine-related peritumoral oedema. Minor toxicities were recorded in four out of 12 patients. In six patients with postoperative residual tumour, vaccination induced one stable disease during 8 weeks, and one partial response. Two of six patients with complete resection are in CCR for 3 years. Tumour vaccination for patients with relapsed malignant glioma is feasible and likely beneficial for patients with minimal residual tumour burden. |
format | Text |
id | pubmed-2409960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-24099602009-09-10 Surgery and adjuvant dendritic cell-based tumour vaccination for patients with relapsed malignant glioma, a feasibility study Rutkowski, S De Vleeschouwer, S Kaempgen, E Wolff, J E A Kühl, J Demaerel, P Warmuth-Metz, M Flamen, P Van Calenbergh, F Plets, C Sörensen, N Opitz, A Van Gool, S W Br J Cancer Clinical Patients with relapsed malignant glioma have a poor prognosis. We developed a strategy of vaccination using autologous mature dendritic cells loaded with autologous tumour homogenate. In total, 12 patients with a median age of 36 years (range: 11–78) were treated. All had relapsing malignant glioma. After surgery, vaccines were given at weeks 1 and 3, and later every 4 weeks. A median of 5 (range: 2–7) vaccines was given. There were no serious adverse events except in one patient with gross residual tumour prior to vaccination, who repetitively developed vaccine-related peritumoral oedema. Minor toxicities were recorded in four out of 12 patients. In six patients with postoperative residual tumour, vaccination induced one stable disease during 8 weeks, and one partial response. Two of six patients with complete resection are in CCR for 3 years. Tumour vaccination for patients with relapsed malignant glioma is feasible and likely beneficial for patients with minimal residual tumour burden. Nature Publishing Group 2004-11-01 2004-10-12 /pmc/articles/PMC2409960/ /pubmed/15477864 http://dx.doi.org/10.1038/sj.bjc.6602195 Text en Copyright © 2004 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Rutkowski, S De Vleeschouwer, S Kaempgen, E Wolff, J E A Kühl, J Demaerel, P Warmuth-Metz, M Flamen, P Van Calenbergh, F Plets, C Sörensen, N Opitz, A Van Gool, S W Surgery and adjuvant dendritic cell-based tumour vaccination for patients with relapsed malignant glioma, a feasibility study |
title | Surgery and adjuvant dendritic cell-based tumour vaccination for patients with relapsed malignant glioma, a feasibility study |
title_full | Surgery and adjuvant dendritic cell-based tumour vaccination for patients with relapsed malignant glioma, a feasibility study |
title_fullStr | Surgery and adjuvant dendritic cell-based tumour vaccination for patients with relapsed malignant glioma, a feasibility study |
title_full_unstemmed | Surgery and adjuvant dendritic cell-based tumour vaccination for patients with relapsed malignant glioma, a feasibility study |
title_short | Surgery and adjuvant dendritic cell-based tumour vaccination for patients with relapsed malignant glioma, a feasibility study |
title_sort | surgery and adjuvant dendritic cell-based tumour vaccination for patients with relapsed malignant glioma, a feasibility study |
topic | Clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409960/ https://www.ncbi.nlm.nih.gov/pubmed/15477864 http://dx.doi.org/10.1038/sj.bjc.6602195 |
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