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Bendamustine or high-dose cytarabine-based induction with rituximab in transplant-eligible mantle cell lymphoma

The objective of this study was to explore differences in outcomes between first-line rituximab plus bendamustine (R-B) and R-CHOP/R-DHAP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone, dexamethasone, cytarabine, cisplatin) in transplant-eligible patients with mantle cell lymphom...

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Autores principales: Villa, Diego, Hoster, Eva, Hermine, Olivier, Klapper, Wolfram, Szymczyk, Michal, Bosly, André, Unterhalt, Michael, Rimsza, Lisa M., Ramsower, Colleen A., Freeman, Ciara L., Scott, David W., Gerrie, Alina S., Savage, Kerry J., Sehn, Laurie H., Dreyling, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Hematology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9631687/
https://www.ncbi.nlm.nih.gov/pubmed/35439293
http://dx.doi.org/10.1182/bloodadvances.2022007371
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author Villa, Diego
Hoster, Eva
Hermine, Olivier
Klapper, Wolfram
Szymczyk, Michal
Bosly, André
Unterhalt, Michael
Rimsza, Lisa M.
Ramsower, Colleen A.
Freeman, Ciara L.
Scott, David W.
Gerrie, Alina S.
Savage, Kerry J.
Sehn, Laurie H.
Dreyling, Martin
author_facet Villa, Diego
Hoster, Eva
Hermine, Olivier
Klapper, Wolfram
Szymczyk, Michal
Bosly, André
Unterhalt, Michael
Rimsza, Lisa M.
Ramsower, Colleen A.
Freeman, Ciara L.
Scott, David W.
Gerrie, Alina S.
Savage, Kerry J.
Sehn, Laurie H.
Dreyling, Martin
author_sort Villa, Diego
collection PubMed
description The objective of this study was to explore differences in outcomes between first-line rituximab plus bendamustine (R-B) and R-CHOP/R-DHAP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone, dexamethasone, cytarabine, cisplatin) in transplant-eligible patients with mantle cell lymphoma (MCL). A population-based cohort of 97 patients aged 18 to 65 years with stage II-IV MCL, consecutively treated with R-B was retrospectively identified at BC Cancer. Baseline characteristics, response rates, and outcomes were compared with the cohort of 232 patients with MCL randomized to the R-CHOP/R-DHAP arm of the MCL Younger trial. The primary endpoint was the hazard ratio (HR) of the progression-free survival (PFS) comparison between both groups, adjusted for MCL International Prognostic Index (MIPI), Ki67 index, and blastoid/ pleomorphic morphology. Ann Arbor stage, lactate dehydrogenase, MIPI, blastoid morphology, and MCL35 assignments were similar between both groups. The overall response rate (ORR) to R-B was 90% (54% complete response [CR]); 77% of patients proceeded to autologous stem cell transplantation (ASCT) and 78% received maintenance rituximab (MR). The ORR to R-CHOP/R-DHAP was 94% (54% CR); 78% proceeded to ASCT and 2% received MR. There were no differences in PFS in unadjusted (HR, 0.87; 95% confidence interval [CI], 0.53-1.41; P = .56) or adjusted (HR, 0.79; 95% CI, 0.45-1.37; P = .40) comparisons. There were no clear differences in secondary endpoints in unadjusted or adjusted analyses. This retrospective adjusted comparison of 2 independent cohorts of younger patients with MCL suggests that R-B with ASCT and maintenance rituximab is a feasible and effective first-line treatment, with outcomes comparable to R-CHOP/R-DHAP with ASCT.
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spelling pubmed-96316872022-11-04 Bendamustine or high-dose cytarabine-based induction with rituximab in transplant-eligible mantle cell lymphoma Villa, Diego Hoster, Eva Hermine, Olivier Klapper, Wolfram Szymczyk, Michal Bosly, André Unterhalt, Michael Rimsza, Lisa M. Ramsower, Colleen A. Freeman, Ciara L. Scott, David W. Gerrie, Alina S. Savage, Kerry J. Sehn, Laurie H. Dreyling, Martin Blood Adv Lymphoid Neoplasia The objective of this study was to explore differences in outcomes between first-line rituximab plus bendamustine (R-B) and R-CHOP/R-DHAP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone, dexamethasone, cytarabine, cisplatin) in transplant-eligible patients with mantle cell lymphoma (MCL). A population-based cohort of 97 patients aged 18 to 65 years with stage II-IV MCL, consecutively treated with R-B was retrospectively identified at BC Cancer. Baseline characteristics, response rates, and outcomes were compared with the cohort of 232 patients with MCL randomized to the R-CHOP/R-DHAP arm of the MCL Younger trial. The primary endpoint was the hazard ratio (HR) of the progression-free survival (PFS) comparison between both groups, adjusted for MCL International Prognostic Index (MIPI), Ki67 index, and blastoid/ pleomorphic morphology. Ann Arbor stage, lactate dehydrogenase, MIPI, blastoid morphology, and MCL35 assignments were similar between both groups. The overall response rate (ORR) to R-B was 90% (54% complete response [CR]); 77% of patients proceeded to autologous stem cell transplantation (ASCT) and 78% received maintenance rituximab (MR). The ORR to R-CHOP/R-DHAP was 94% (54% CR); 78% proceeded to ASCT and 2% received MR. There were no differences in PFS in unadjusted (HR, 0.87; 95% confidence interval [CI], 0.53-1.41; P = .56) or adjusted (HR, 0.79; 95% CI, 0.45-1.37; P = .40) comparisons. There were no clear differences in secondary endpoints in unadjusted or adjusted analyses. This retrospective adjusted comparison of 2 independent cohorts of younger patients with MCL suggests that R-B with ASCT and maintenance rituximab is a feasible and effective first-line treatment, with outcomes comparable to R-CHOP/R-DHAP with ASCT. American Society of Hematology 2022-09-19 /pmc/articles/PMC9631687/ /pubmed/35439293 http://dx.doi.org/10.1182/bloodadvances.2022007371 Text en © 2022 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.
spellingShingle Lymphoid Neoplasia
Villa, Diego
Hoster, Eva
Hermine, Olivier
Klapper, Wolfram
Szymczyk, Michal
Bosly, André
Unterhalt, Michael
Rimsza, Lisa M.
Ramsower, Colleen A.
Freeman, Ciara L.
Scott, David W.
Gerrie, Alina S.
Savage, Kerry J.
Sehn, Laurie H.
Dreyling, Martin
Bendamustine or high-dose cytarabine-based induction with rituximab in transplant-eligible mantle cell lymphoma
title Bendamustine or high-dose cytarabine-based induction with rituximab in transplant-eligible mantle cell lymphoma
title_full Bendamustine or high-dose cytarabine-based induction with rituximab in transplant-eligible mantle cell lymphoma
title_fullStr Bendamustine or high-dose cytarabine-based induction with rituximab in transplant-eligible mantle cell lymphoma
title_full_unstemmed Bendamustine or high-dose cytarabine-based induction with rituximab in transplant-eligible mantle cell lymphoma
title_short Bendamustine or high-dose cytarabine-based induction with rituximab in transplant-eligible mantle cell lymphoma
title_sort bendamustine or high-dose cytarabine-based induction with rituximab in transplant-eligible mantle cell lymphoma
topic Lymphoid Neoplasia
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9631687/
https://www.ncbi.nlm.nih.gov/pubmed/35439293
http://dx.doi.org/10.1182/bloodadvances.2022007371
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