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Bendamustine combined with rituximab for patients with relapsed or refractory diffuse large B cell lymphoma

Patients with relapsed or refractory diffuse large B cell lymphoma (DLBCL) are treated with salvage regimens and may be considered for high-dose chemotherapy and autologous stem cell transplantation if disease is chemosensitive. Bendamustine is active in indolent B cell lymphomas and chronic lymphoc...

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Autores principales: Vacirca, Jeffrey L., Acs, Peter. I., Tabbara, Imad A., Rosen, Peter. J., Lee, Peter, Lynam, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3918114/
https://www.ncbi.nlm.nih.gov/pubmed/23955074
http://dx.doi.org/10.1007/s00277-013-1879-x
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author Vacirca, Jeffrey L.
Acs, Peter. I.
Tabbara, Imad A.
Rosen, Peter. J.
Lee, Peter
Lynam, Eric
author_facet Vacirca, Jeffrey L.
Acs, Peter. I.
Tabbara, Imad A.
Rosen, Peter. J.
Lee, Peter
Lynam, Eric
author_sort Vacirca, Jeffrey L.
collection PubMed
description Patients with relapsed or refractory diffuse large B cell lymphoma (DLBCL) are treated with salvage regimens and may be considered for high-dose chemotherapy and autologous stem cell transplantation if disease is chemosensitive. Bendamustine is active in indolent B cell lymphomas and chronic lymphocytic leukemia but has not been extensively studied in aggressive lymphomas. This trial examines the combination of bendamustine and rituximab in patients with relapsed and refractory DLBCL. Patients received bendamustine at 90 mg/m(2) (n = 2) or 120 mg/m(2) (n = 57) on days 1 and 2 and rituximab at 375 mg/m(2) on day 1 every 28 days for up to 6 cycles. The study evaluated objective response rate (ORR), duration of response (DOR), progression-free survival (PFS), and treatment safety. Fifty-nine patients were treated, and 48 were evaluable for response. Median age was 74; 89 % had stage III or IV disease, and 63 % had high revised International Prognostic Index scores; the median number of prior therapies was 1. Based on analysis using the intent-to-treat population, the ORR was 45.8 % (complete response, 15.3 %; partial response, 30.5 %). The median DOR was 17.3 months, and the median PFS was 3.6 months. Grade 3 or 4 hematological toxicities included neutropenia (36 %), leukopenia (29 %), thrombocytopenia (22 %), and anemia (12 %). The combination of bendamustine and rituximab showed modest activity in patients with relapsed and refractory DLBCL and has an acceptable toxicity profile.
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spelling pubmed-39181142014-02-14 Bendamustine combined with rituximab for patients with relapsed or refractory diffuse large B cell lymphoma Vacirca, Jeffrey L. Acs, Peter. I. Tabbara, Imad A. Rosen, Peter. J. Lee, Peter Lynam, Eric Ann Hematol Original Article Patients with relapsed or refractory diffuse large B cell lymphoma (DLBCL) are treated with salvage regimens and may be considered for high-dose chemotherapy and autologous stem cell transplantation if disease is chemosensitive. Bendamustine is active in indolent B cell lymphomas and chronic lymphocytic leukemia but has not been extensively studied in aggressive lymphomas. This trial examines the combination of bendamustine and rituximab in patients with relapsed and refractory DLBCL. Patients received bendamustine at 90 mg/m(2) (n = 2) or 120 mg/m(2) (n = 57) on days 1 and 2 and rituximab at 375 mg/m(2) on day 1 every 28 days for up to 6 cycles. The study evaluated objective response rate (ORR), duration of response (DOR), progression-free survival (PFS), and treatment safety. Fifty-nine patients were treated, and 48 were evaluable for response. Median age was 74; 89 % had stage III or IV disease, and 63 % had high revised International Prognostic Index scores; the median number of prior therapies was 1. Based on analysis using the intent-to-treat population, the ORR was 45.8 % (complete response, 15.3 %; partial response, 30.5 %). The median DOR was 17.3 months, and the median PFS was 3.6 months. Grade 3 or 4 hematological toxicities included neutropenia (36 %), leukopenia (29 %), thrombocytopenia (22 %), and anemia (12 %). The combination of bendamustine and rituximab showed modest activity in patients with relapsed and refractory DLBCL and has an acceptable toxicity profile. Springer Berlin Heidelberg 2013-08-17 2014 /pmc/articles/PMC3918114/ /pubmed/23955074 http://dx.doi.org/10.1007/s00277-013-1879-x Text en © The Author(s) 2013 https://creativecommons.org/licenses/by-nc/2.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Vacirca, Jeffrey L.
Acs, Peter. I.
Tabbara, Imad A.
Rosen, Peter. J.
Lee, Peter
Lynam, Eric
Bendamustine combined with rituximab for patients with relapsed or refractory diffuse large B cell lymphoma
title Bendamustine combined with rituximab for patients with relapsed or refractory diffuse large B cell lymphoma
title_full Bendamustine combined with rituximab for patients with relapsed or refractory diffuse large B cell lymphoma
title_fullStr Bendamustine combined with rituximab for patients with relapsed or refractory diffuse large B cell lymphoma
title_full_unstemmed Bendamustine combined with rituximab for patients with relapsed or refractory diffuse large B cell lymphoma
title_short Bendamustine combined with rituximab for patients with relapsed or refractory diffuse large B cell lymphoma
title_sort bendamustine combined with rituximab for patients with relapsed or refractory diffuse large b cell lymphoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3918114/
https://www.ncbi.nlm.nih.gov/pubmed/23955074
http://dx.doi.org/10.1007/s00277-013-1879-x
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