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Primary therapy with single agent bortezomib as induction, maintenance, and re-Induction in patients with high risk myeloma: results of the ECOG E2A02 trial
Single agent bortezomib results in response rates of 51% in patients with newly diagnosed multiple myeloma (MM) and is touted to be especially effective in high-risk disease. We are the first to prospectively explore single agent bortezomib as primary therapy (response rate, maintenance and reinduct...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2921007/ https://www.ncbi.nlm.nih.gov/pubmed/20535147 http://dx.doi.org/10.1038/leu.2010.129 |
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author | Dispenzieri, Angela Jacobus, Susanna Vesole, David H. Callandar, Natalie Fonseca, Rafael Greipp, Philip R. |
author_facet | Dispenzieri, Angela Jacobus, Susanna Vesole, David H. Callandar, Natalie Fonseca, Rafael Greipp, Philip R. |
author_sort | Dispenzieri, Angela |
collection | PubMed |
description | Single agent bortezomib results in response rates of 51% in patients with newly diagnosed multiple myeloma (MM) and is touted to be especially effective in high-risk disease. We are the first to prospectively explore single agent bortezomib as primary therapy (response rate, maintenance and reinduction) without consolidative autologous stem cell transplant in a cohort selected to have high-risk MM. Patients received 8-cycles of induction followed by maintenance bortezomib every other week indefinitely. Patients relapsing on maintenance had full induction schedule resumed. On an intention to treat basis the response rate (>=PR) was 48%. Among 7 patients, who progressed on maintenance bortezomib and received reinduction, two responded. With a median follow-up of 48.2 months, 1- and 2-year OS probabilities were 88% (95%CI, 74–95%) and 76% (95%CI, 60–86%), respectively. Median PFS was 7.9 months (95%CI, 5.8–12.0). Twenty-three and 34 patients had >=grade 3 hematologic and non-hematologic toxicity, respectively with treatment emergent neuropathy in: 7%, motor grade 1–2; 56%, sensory grade 1–2 and 2%, grade 3; and 14%, neuropathic pain grade 1–2 in and 2%, grade 3. In high-risk patients, upfront bortezomib results in response rates comparable to those reported for unselected cohorts, but single agent bortezomib is not sufficient as primary therapy. |
format | Text |
id | pubmed-2921007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
record_format | MEDLINE/PubMed |
spelling | pubmed-29210072011-02-01 Primary therapy with single agent bortezomib as induction, maintenance, and re-Induction in patients with high risk myeloma: results of the ECOG E2A02 trial Dispenzieri, Angela Jacobus, Susanna Vesole, David H. Callandar, Natalie Fonseca, Rafael Greipp, Philip R. Leukemia Article Single agent bortezomib results in response rates of 51% in patients with newly diagnosed multiple myeloma (MM) and is touted to be especially effective in high-risk disease. We are the first to prospectively explore single agent bortezomib as primary therapy (response rate, maintenance and reinduction) without consolidative autologous stem cell transplant in a cohort selected to have high-risk MM. Patients received 8-cycles of induction followed by maintenance bortezomib every other week indefinitely. Patients relapsing on maintenance had full induction schedule resumed. On an intention to treat basis the response rate (>=PR) was 48%. Among 7 patients, who progressed on maintenance bortezomib and received reinduction, two responded. With a median follow-up of 48.2 months, 1- and 2-year OS probabilities were 88% (95%CI, 74–95%) and 76% (95%CI, 60–86%), respectively. Median PFS was 7.9 months (95%CI, 5.8–12.0). Twenty-three and 34 patients had >=grade 3 hematologic and non-hematologic toxicity, respectively with treatment emergent neuropathy in: 7%, motor grade 1–2; 56%, sensory grade 1–2 and 2%, grade 3; and 14%, neuropathic pain grade 1–2 in and 2%, grade 3. In high-risk patients, upfront bortezomib results in response rates comparable to those reported for unselected cohorts, but single agent bortezomib is not sufficient as primary therapy. 2010-06-10 2010-08 /pmc/articles/PMC2921007/ /pubmed/20535147 http://dx.doi.org/10.1038/leu.2010.129 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Dispenzieri, Angela Jacobus, Susanna Vesole, David H. Callandar, Natalie Fonseca, Rafael Greipp, Philip R. Primary therapy with single agent bortezomib as induction, maintenance, and re-Induction in patients with high risk myeloma: results of the ECOG E2A02 trial |
title | Primary therapy with single agent bortezomib as induction, maintenance, and re-Induction in patients with high risk myeloma: results of the ECOG E2A02 trial |
title_full | Primary therapy with single agent bortezomib as induction, maintenance, and re-Induction in patients with high risk myeloma: results of the ECOG E2A02 trial |
title_fullStr | Primary therapy with single agent bortezomib as induction, maintenance, and re-Induction in patients with high risk myeloma: results of the ECOG E2A02 trial |
title_full_unstemmed | Primary therapy with single agent bortezomib as induction, maintenance, and re-Induction in patients with high risk myeloma: results of the ECOG E2A02 trial |
title_short | Primary therapy with single agent bortezomib as induction, maintenance, and re-Induction in patients with high risk myeloma: results of the ECOG E2A02 trial |
title_sort | primary therapy with single agent bortezomib as induction, maintenance, and re-induction in patients with high risk myeloma: results of the ecog e2a02 trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2921007/ https://www.ncbi.nlm.nih.gov/pubmed/20535147 http://dx.doi.org/10.1038/leu.2010.129 |
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