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Is there a role for ‘modified VAD’ in the treatment of multiple myeloma?
VAD, (Vincristine, Doxorubicin and Dexamethasone) was initially proposed as a salvage therapy for myeloma patients in whom prior alkylating agent therapy failed, although in recent years VAD has been surpassed by novel combination therapies with new biological agents such as thalidomide (and its der...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cancer Intelligence
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223996/ https://www.ncbi.nlm.nih.gov/pubmed/22276003 http://dx.doi.org/10.3332/ecancer.2009.136 |
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author | Agazzi, A Sammassimo, S Laszlo, D Liptrott, SJ Cascio, R Alietti, A Rabascio, C Mancuso, P Pruneri, G Martinelli, G |
author_facet | Agazzi, A Sammassimo, S Laszlo, D Liptrott, SJ Cascio, R Alietti, A Rabascio, C Mancuso, P Pruneri, G Martinelli, G |
author_sort | Agazzi, A |
collection | PubMed |
description | VAD, (Vincristine, Doxorubicin and Dexamethasone) was initially proposed as a salvage therapy for myeloma patients in whom prior alkylating agent therapy failed, although in recent years VAD has been surpassed by novel combination therapies with new biological agents such as thalidomide (and its derivative, lenalidomide) and bortezomib. After the excellent results obtained by the novel agents, VAD can no longer be proposed in preparation to autologous transplantation, although there are still indications that VAD remains useful and clinically relevant in the initial treatment of symptomatic multiple myeloma. |
format | Online Article Text |
id | pubmed-3223996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Cancer Intelligence |
record_format | MEDLINE/PubMed |
spelling | pubmed-32239962012-01-24 Is there a role for ‘modified VAD’ in the treatment of multiple myeloma? Agazzi, A Sammassimo, S Laszlo, D Liptrott, SJ Cascio, R Alietti, A Rabascio, C Mancuso, P Pruneri, G Martinelli, G Ecancermedicalscience Research Article VAD, (Vincristine, Doxorubicin and Dexamethasone) was initially proposed as a salvage therapy for myeloma patients in whom prior alkylating agent therapy failed, although in recent years VAD has been surpassed by novel combination therapies with new biological agents such as thalidomide (and its derivative, lenalidomide) and bortezomib. After the excellent results obtained by the novel agents, VAD can no longer be proposed in preparation to autologous transplantation, although there are still indications that VAD remains useful and clinically relevant in the initial treatment of symptomatic multiple myeloma. Cancer Intelligence 2009-06-04 /pmc/articles/PMC3223996/ /pubmed/22276003 http://dx.doi.org/10.3332/ecancer.2009.136 Text en © the authors; licensee ecancermedicalscience. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Agazzi, A Sammassimo, S Laszlo, D Liptrott, SJ Cascio, R Alietti, A Rabascio, C Mancuso, P Pruneri, G Martinelli, G Is there a role for ‘modified VAD’ in the treatment of multiple myeloma? |
title | Is there a role for ‘modified VAD’ in the treatment of multiple myeloma? |
title_full | Is there a role for ‘modified VAD’ in the treatment of multiple myeloma? |
title_fullStr | Is there a role for ‘modified VAD’ in the treatment of multiple myeloma? |
title_full_unstemmed | Is there a role for ‘modified VAD’ in the treatment of multiple myeloma? |
title_short | Is there a role for ‘modified VAD’ in the treatment of multiple myeloma? |
title_sort | is there a role for ‘modified vad’ in the treatment of multiple myeloma? |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223996/ https://www.ncbi.nlm.nih.gov/pubmed/22276003 http://dx.doi.org/10.3332/ecancer.2009.136 |
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