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Dose-dense and less dose-intense Total Therapy 5 for gene expression profiling-defined high-risk multiple myeloma
Multiple myeloma (MM) is a heterogeneous disease with high-risk patients progressing rapidly despite treatment. Various definitions of high-risk MM are used and we reported that gene expression profile (GEP)-defined high risk was a major predictor of relapse. In spite of our best efforts, the majori...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030385/ https://www.ncbi.nlm.nih.gov/pubmed/27471869 http://dx.doi.org/10.1038/bcj.2016.64 |
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author | Jethava, Y Mitchell, A Zangari, M Waheed, S Schinke, C Thanendrarajan, S Sawyer, J Alapat, D Tian, E Stein, C Khan, R Heuck, C J Petty, N Avery, D Steward, D Smith, R Bailey, C Epstein, J Yaccoby, S Hoering, A Crowley, J Morgan, G Barlogie, B van Rhee, F |
author_facet | Jethava, Y Mitchell, A Zangari, M Waheed, S Schinke, C Thanendrarajan, S Sawyer, J Alapat, D Tian, E Stein, C Khan, R Heuck, C J Petty, N Avery, D Steward, D Smith, R Bailey, C Epstein, J Yaccoby, S Hoering, A Crowley, J Morgan, G Barlogie, B van Rhee, F |
author_sort | Jethava, Y |
collection | PubMed |
description | Multiple myeloma (MM) is a heterogeneous disease with high-risk patients progressing rapidly despite treatment. Various definitions of high-risk MM are used and we reported that gene expression profile (GEP)-defined high risk was a major predictor of relapse. In spite of our best efforts, the majority of GEP70 high-risk patients relapse and we have noted higher relapse rates during drug-free intervals. This prompted us to explore the concept of less intense drug dosing with shorter intervals between courses with the aim of preventing inter-course relapse. Here we report the outcome of the Total Therapy 5 trial, where this concept was tested. This regimen effectively reduced early mortality and relapse but failed to improve progression-free survival and overall survival due to relapse early during maintenance. |
format | Online Article Text |
id | pubmed-5030385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50303852016-09-26 Dose-dense and less dose-intense Total Therapy 5 for gene expression profiling-defined high-risk multiple myeloma Jethava, Y Mitchell, A Zangari, M Waheed, S Schinke, C Thanendrarajan, S Sawyer, J Alapat, D Tian, E Stein, C Khan, R Heuck, C J Petty, N Avery, D Steward, D Smith, R Bailey, C Epstein, J Yaccoby, S Hoering, A Crowley, J Morgan, G Barlogie, B van Rhee, F Blood Cancer J Original Article Multiple myeloma (MM) is a heterogeneous disease with high-risk patients progressing rapidly despite treatment. Various definitions of high-risk MM are used and we reported that gene expression profile (GEP)-defined high risk was a major predictor of relapse. In spite of our best efforts, the majority of GEP70 high-risk patients relapse and we have noted higher relapse rates during drug-free intervals. This prompted us to explore the concept of less intense drug dosing with shorter intervals between courses with the aim of preventing inter-course relapse. Here we report the outcome of the Total Therapy 5 trial, where this concept was tested. This regimen effectively reduced early mortality and relapse but failed to improve progression-free survival and overall survival due to relapse early during maintenance. Nature Publishing Group 2016-07 2016-07-29 /pmc/articles/PMC5030385/ /pubmed/27471869 http://dx.doi.org/10.1038/bcj.2016.64 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Jethava, Y Mitchell, A Zangari, M Waheed, S Schinke, C Thanendrarajan, S Sawyer, J Alapat, D Tian, E Stein, C Khan, R Heuck, C J Petty, N Avery, D Steward, D Smith, R Bailey, C Epstein, J Yaccoby, S Hoering, A Crowley, J Morgan, G Barlogie, B van Rhee, F Dose-dense and less dose-intense Total Therapy 5 for gene expression profiling-defined high-risk multiple myeloma |
title | Dose-dense and less dose-intense Total Therapy 5 for gene expression profiling-defined high-risk multiple myeloma |
title_full | Dose-dense and less dose-intense Total Therapy 5 for gene expression profiling-defined high-risk multiple myeloma |
title_fullStr | Dose-dense and less dose-intense Total Therapy 5 for gene expression profiling-defined high-risk multiple myeloma |
title_full_unstemmed | Dose-dense and less dose-intense Total Therapy 5 for gene expression profiling-defined high-risk multiple myeloma |
title_short | Dose-dense and less dose-intense Total Therapy 5 for gene expression profiling-defined high-risk multiple myeloma |
title_sort | dose-dense and less dose-intense total therapy 5 for gene expression profiling-defined high-risk multiple myeloma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030385/ https://www.ncbi.nlm.nih.gov/pubmed/27471869 http://dx.doi.org/10.1038/bcj.2016.64 |
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