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Multi-center phase II trial of bortezomib and rituximab maintenance combination therapy in patients with mantle cell lymphoma after consolidative autologous stem cell transplantation
BACKGROUND: Mantle cell lymphoma (MCL) is an aggressive and incurable lymphoma. Standard of care for younger patients with MCL is induction chemotherapy followed by autologous stem cell transplantation (auto-HCT). Rituximab maintenance after auto-HCT has been shown to improve progression-free surviv...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022297/ https://www.ncbi.nlm.nih.gov/pubmed/29954415 http://dx.doi.org/10.1186/s13045-018-0631-3 |
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author | Chen, Robert W. Palmer, Joycelynne M. Tomassetti, Sarah Popplewell, Leslie L. Alluin, Jessica Chomchan, Pritsana Nademanee, Auayporn P. Siddiqi, Tanya Tsai, Ni-Chun Chen, Lu Zuo, Fay Abary, Rosemarie Cai, Ji-lian Herrera, Alex F. Rossi, John J. Rosen, Steven T. Forman, Stephen J. Kwak, Larry W. Holmberg, Leona A. |
author_facet | Chen, Robert W. Palmer, Joycelynne M. Tomassetti, Sarah Popplewell, Leslie L. Alluin, Jessica Chomchan, Pritsana Nademanee, Auayporn P. Siddiqi, Tanya Tsai, Ni-Chun Chen, Lu Zuo, Fay Abary, Rosemarie Cai, Ji-lian Herrera, Alex F. Rossi, John J. Rosen, Steven T. Forman, Stephen J. Kwak, Larry W. Holmberg, Leona A. |
author_sort | Chen, Robert W. |
collection | PubMed |
description | BACKGROUND: Mantle cell lymphoma (MCL) is an aggressive and incurable lymphoma. Standard of care for younger patients with MCL is induction chemotherapy followed by autologous stem cell transplantation (auto-HCT). Rituximab maintenance after auto-HCT has been shown to improve progression-free survival (PFS) and overall survival (OS) in MCL. Bortezomib maintenance therapy has also been shown to be tolerable and feasible in this setting. However, the combination of bortezomib and rituximab as maintenance therapy post-auto-HCT has not been studied. METHODS: We conducted a multicenter, phase II trial of bortezomib given in combination with rituximab as maintenance in MCL patients after consolidative auto-HCT. Enrolled patients (n = 23) received bortezomib 1.3 mg/m(2) subcutaneously weekly for 4 weeks every 3 months (up to 24 months) and rituximab 375 mg/m(2) intravenously weekly for 4 weeks every 6 months (up to 24 months) for a total duration of 2 years. The primary study endpoint was disease-free survival (DFS). RESULTS: With a median follow-up of 35.9 months, the 2-year DFS probability was 90.2% (95% CI 66–97), and 2-year OS was 94.7% (95% CI 68–99). The most frequent grade 3/4 toxic events were neutropenia (in 74% of patients) and lymphopenia (in 35%). The incidence of peripheral neuropathy was 48% for grade 1, 9% for grade 2, and 0% for grade 3/4. We also examined the role of quantitative cyclin D1 (CCND1) mRNA in monitoring minimal residual disease. CONCLUSION: Combined bortezomib and rituximab as maintenance therapy in MCL patients following auto-HCT is an active and well-tolerated regimen. TRIAL REGISTRATION: ClinicalTrials.gov NCT01267812, registered Dec 29, 2010. |
format | Online Article Text |
id | pubmed-6022297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60222972018-07-09 Multi-center phase II trial of bortezomib and rituximab maintenance combination therapy in patients with mantle cell lymphoma after consolidative autologous stem cell transplantation Chen, Robert W. Palmer, Joycelynne M. Tomassetti, Sarah Popplewell, Leslie L. Alluin, Jessica Chomchan, Pritsana Nademanee, Auayporn P. Siddiqi, Tanya Tsai, Ni-Chun Chen, Lu Zuo, Fay Abary, Rosemarie Cai, Ji-lian Herrera, Alex F. Rossi, John J. Rosen, Steven T. Forman, Stephen J. Kwak, Larry W. Holmberg, Leona A. J Hematol Oncol Research BACKGROUND: Mantle cell lymphoma (MCL) is an aggressive and incurable lymphoma. Standard of care for younger patients with MCL is induction chemotherapy followed by autologous stem cell transplantation (auto-HCT). Rituximab maintenance after auto-HCT has been shown to improve progression-free survival (PFS) and overall survival (OS) in MCL. Bortezomib maintenance therapy has also been shown to be tolerable and feasible in this setting. However, the combination of bortezomib and rituximab as maintenance therapy post-auto-HCT has not been studied. METHODS: We conducted a multicenter, phase II trial of bortezomib given in combination with rituximab as maintenance in MCL patients after consolidative auto-HCT. Enrolled patients (n = 23) received bortezomib 1.3 mg/m(2) subcutaneously weekly for 4 weeks every 3 months (up to 24 months) and rituximab 375 mg/m(2) intravenously weekly for 4 weeks every 6 months (up to 24 months) for a total duration of 2 years. The primary study endpoint was disease-free survival (DFS). RESULTS: With a median follow-up of 35.9 months, the 2-year DFS probability was 90.2% (95% CI 66–97), and 2-year OS was 94.7% (95% CI 68–99). The most frequent grade 3/4 toxic events were neutropenia (in 74% of patients) and lymphopenia (in 35%). The incidence of peripheral neuropathy was 48% for grade 1, 9% for grade 2, and 0% for grade 3/4. We also examined the role of quantitative cyclin D1 (CCND1) mRNA in monitoring minimal residual disease. CONCLUSION: Combined bortezomib and rituximab as maintenance therapy in MCL patients following auto-HCT is an active and well-tolerated regimen. TRIAL REGISTRATION: ClinicalTrials.gov NCT01267812, registered Dec 29, 2010. BioMed Central 2018-06-28 /pmc/articles/PMC6022297/ /pubmed/29954415 http://dx.doi.org/10.1186/s13045-018-0631-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Chen, Robert W. Palmer, Joycelynne M. Tomassetti, Sarah Popplewell, Leslie L. Alluin, Jessica Chomchan, Pritsana Nademanee, Auayporn P. Siddiqi, Tanya Tsai, Ni-Chun Chen, Lu Zuo, Fay Abary, Rosemarie Cai, Ji-lian Herrera, Alex F. Rossi, John J. Rosen, Steven T. Forman, Stephen J. Kwak, Larry W. Holmberg, Leona A. Multi-center phase II trial of bortezomib and rituximab maintenance combination therapy in patients with mantle cell lymphoma after consolidative autologous stem cell transplantation |
title | Multi-center phase II trial of bortezomib and rituximab maintenance combination therapy in patients with mantle cell lymphoma after consolidative autologous stem cell transplantation |
title_full | Multi-center phase II trial of bortezomib and rituximab maintenance combination therapy in patients with mantle cell lymphoma after consolidative autologous stem cell transplantation |
title_fullStr | Multi-center phase II trial of bortezomib and rituximab maintenance combination therapy in patients with mantle cell lymphoma after consolidative autologous stem cell transplantation |
title_full_unstemmed | Multi-center phase II trial of bortezomib and rituximab maintenance combination therapy in patients with mantle cell lymphoma after consolidative autologous stem cell transplantation |
title_short | Multi-center phase II trial of bortezomib and rituximab maintenance combination therapy in patients with mantle cell lymphoma after consolidative autologous stem cell transplantation |
title_sort | multi-center phase ii trial of bortezomib and rituximab maintenance combination therapy in patients with mantle cell lymphoma after consolidative autologous stem cell transplantation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022297/ https://www.ncbi.nlm.nih.gov/pubmed/29954415 http://dx.doi.org/10.1186/s13045-018-0631-3 |
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