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Thalidomide and dexamethasone vs. bortezomib and dexamethasone for melphalan refractory myeloma: a randomized study
OBJECTIVES: Thalidomide and bortezomib have been frequently used for second-line therapy in patients with myeloma relapsing after or refractory to initial melphalan-based treatment, but no randomized trials have been published comparing these two treatment alternatives. METHODS: Thalidomide- and bor...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492844/ https://www.ncbi.nlm.nih.gov/pubmed/22404182 http://dx.doi.org/10.1111/j.1600-0609.2012.01775.x |
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author | Hjorth, Martin Hjertner, Øyvind Knudsen, Lene Meldgaard Gulbrandsen, Nina Holmberg, Erik Pedersen, Per Trøllund Andersen, Niels Frost Andréasson, Björn Billström, Rolf Carlson, Kristina Carlsson, Margaretha S Flogegård, Max Forsberg, Karin Gimsing, Peter Karlsson, Torbjörn Linder, Olle Nahi, Hareth Othzén, Annika Swedin, Agneta |
author_facet | Hjorth, Martin Hjertner, Øyvind Knudsen, Lene Meldgaard Gulbrandsen, Nina Holmberg, Erik Pedersen, Per Trøllund Andersen, Niels Frost Andréasson, Björn Billström, Rolf Carlson, Kristina Carlsson, Margaretha S Flogegård, Max Forsberg, Karin Gimsing, Peter Karlsson, Torbjörn Linder, Olle Nahi, Hareth Othzén, Annika Swedin, Agneta |
author_sort | Hjorth, Martin |
collection | PubMed |
description | OBJECTIVES: Thalidomide and bortezomib have been frequently used for second-line therapy in patients with myeloma relapsing after or refractory to initial melphalan-based treatment, but no randomized trials have been published comparing these two treatment alternatives. METHODS: Thalidomide- and bortezomib-naïve patients with melphalan refractory myeloma were randomly assigned to low-dose thalidomide + dexamethasone (Thal-Dex) or bortezomib + dexamethasone (Bort-Dex). At progression on either therapy, the patients were offered crossover to the alternative drug combination. An estimated 300 patients would be needed for the trial to detect a 50% difference in median PFS between the treatment arms. RESULTS: After inclusion of 131 patients, the trial was prematurely closed because of low accrual. Sixty-seven patients were randomized to Thal-Dex and 64 to Bort-Dex. Progression-free survival was similar (median, 9.0 months for Thal-Dex and 7.2 for Bort-Dex). Response rate was similar (55% for Thal-Dex and 63% for Bort-Dex), but time to response was shorter (P < 0.05) and the VGPR rate higher (P < 0.01) for Bort-Dex. Time-to-other treatment after crossover was similar (median, 13.2 months for Thal-Dex and 11.2 months for Bort-Dex), as was overall survival (22.8 months for Thal-Dex and 19.0 for Bort-Dex). Venous thromboembolism was seen in seven patients and cerebrovascular events in four patients in the Thal-Dex group. Severe neuropathy, reactivation of herpes virus infections, and mental depression were more frequently observed in the Bort-Dex group. In the quality-of-life analysis, no difference was noted for physical function, pain, and global quality of life. Fatigue and sleep disturbances were significantly more prevalent in the Bort-Dex group. CONCLUSIONS: Thalidomide (50–100 mg daily) in combination with dexamethasone seems to have an efficacy comparable with that of bortezomib and dexamethasone in melphalan refractory myeloma. However, the statistical strength of the results in this study is limited by the low number of included patients. |
format | Online Article Text |
id | pubmed-3492844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-34928442012-11-09 Thalidomide and dexamethasone vs. bortezomib and dexamethasone for melphalan refractory myeloma: a randomized study Hjorth, Martin Hjertner, Øyvind Knudsen, Lene Meldgaard Gulbrandsen, Nina Holmberg, Erik Pedersen, Per Trøllund Andersen, Niels Frost Andréasson, Björn Billström, Rolf Carlson, Kristina Carlsson, Margaretha S Flogegård, Max Forsberg, Karin Gimsing, Peter Karlsson, Torbjörn Linder, Olle Nahi, Hareth Othzén, Annika Swedin, Agneta Eur J Haematol Original Articles OBJECTIVES: Thalidomide and bortezomib have been frequently used for second-line therapy in patients with myeloma relapsing after or refractory to initial melphalan-based treatment, but no randomized trials have been published comparing these two treatment alternatives. METHODS: Thalidomide- and bortezomib-naïve patients with melphalan refractory myeloma were randomly assigned to low-dose thalidomide + dexamethasone (Thal-Dex) or bortezomib + dexamethasone (Bort-Dex). At progression on either therapy, the patients were offered crossover to the alternative drug combination. An estimated 300 patients would be needed for the trial to detect a 50% difference in median PFS between the treatment arms. RESULTS: After inclusion of 131 patients, the trial was prematurely closed because of low accrual. Sixty-seven patients were randomized to Thal-Dex and 64 to Bort-Dex. Progression-free survival was similar (median, 9.0 months for Thal-Dex and 7.2 for Bort-Dex). Response rate was similar (55% for Thal-Dex and 63% for Bort-Dex), but time to response was shorter (P < 0.05) and the VGPR rate higher (P < 0.01) for Bort-Dex. Time-to-other treatment after crossover was similar (median, 13.2 months for Thal-Dex and 11.2 months for Bort-Dex), as was overall survival (22.8 months for Thal-Dex and 19.0 for Bort-Dex). Venous thromboembolism was seen in seven patients and cerebrovascular events in four patients in the Thal-Dex group. Severe neuropathy, reactivation of herpes virus infections, and mental depression were more frequently observed in the Bort-Dex group. In the quality-of-life analysis, no difference was noted for physical function, pain, and global quality of life. Fatigue and sleep disturbances were significantly more prevalent in the Bort-Dex group. CONCLUSIONS: Thalidomide (50–100 mg daily) in combination with dexamethasone seems to have an efficacy comparable with that of bortezomib and dexamethasone in melphalan refractory myeloma. However, the statistical strength of the results in this study is limited by the low number of included patients. Blackwell Publishing Ltd 2012-06 /pmc/articles/PMC3492844/ /pubmed/22404182 http://dx.doi.org/10.1111/j.1600-0609.2012.01775.x Text en © 2012 John Wiley & Sons A/S http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Articles Hjorth, Martin Hjertner, Øyvind Knudsen, Lene Meldgaard Gulbrandsen, Nina Holmberg, Erik Pedersen, Per Trøllund Andersen, Niels Frost Andréasson, Björn Billström, Rolf Carlson, Kristina Carlsson, Margaretha S Flogegård, Max Forsberg, Karin Gimsing, Peter Karlsson, Torbjörn Linder, Olle Nahi, Hareth Othzén, Annika Swedin, Agneta Thalidomide and dexamethasone vs. bortezomib and dexamethasone for melphalan refractory myeloma: a randomized study |
title | Thalidomide and dexamethasone vs. bortezomib and dexamethasone for melphalan refractory myeloma: a randomized study |
title_full | Thalidomide and dexamethasone vs. bortezomib and dexamethasone for melphalan refractory myeloma: a randomized study |
title_fullStr | Thalidomide and dexamethasone vs. bortezomib and dexamethasone for melphalan refractory myeloma: a randomized study |
title_full_unstemmed | Thalidomide and dexamethasone vs. bortezomib and dexamethasone for melphalan refractory myeloma: a randomized study |
title_short | Thalidomide and dexamethasone vs. bortezomib and dexamethasone for melphalan refractory myeloma: a randomized study |
title_sort | thalidomide and dexamethasone vs. bortezomib and dexamethasone for melphalan refractory myeloma: a randomized study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492844/ https://www.ncbi.nlm.nih.gov/pubmed/22404182 http://dx.doi.org/10.1111/j.1600-0609.2012.01775.x |
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