The addition of bortezomib to rituximab, high-dose cytarabine and dexamethasone in relapsed or refractory mantle cell lymphoma—a randomized, open-label phase III trial of the European mantle cell lymphoma network
The therapy of relapsed or refractory (r/r) mantle cell lymphoma (MCL) patients remains a major clinical challenge to date. We conducted a randomized, open-label, parallel-group phase-III trial hypothesizing superior efficacy of rituximab, high-dose cytarabine and dexamethasone with bortezomib (R-HA...
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creator | Fischer, Luca Jiang, Linmiao Dürig, Jan Schmidt, Christian Stilgenbauer, Stephan Bouabdallah, Krimo Solal-Celigny, Philippe Scholz, Christian W. Feugier, Pierre de Wit, Maike Trappe, Ralf Ulrich Hallek, Michael Graeven, Ullrich Hänel, Mathias Hoffmann, Martin Delwail, Vincent Macro, Margaret Greiner, Jochen Giagounidis, Aristoteles A. N. Dargel, Beate Durot, Eric Foussard, Charles Silkenstedt, Elisabeth Weigert, Oliver Pott, Christiane Klapper, Wolfram Hiddemann, Wolfgang Unterhalt, Michael Hoster, Eva Ribrag, Vincent Dreyling, Martin |
description | The therapy of relapsed or refractory (r/r) mantle cell lymphoma (MCL) patients remains a major clinical challenge to date. We conducted a randomized, open-label, parallel-group phase-III trial hypothesizing superior efficacy of rituximab, high-dose cytarabine and dexamethasone with bortezomib (R-HAD + B) versus without (R-HAD) in r/r MCL ineligible for or relapsed after autologous stem cell transplant (ASCT). Primary endpoint was time to treatment failure (TTF), secondary endpoints included response rates, progression free survival, overall survival, and safety. In total, 128 of 175 planned patients were randomized to R-HAD + B (
n
= 64) or R-HAD (
n
= 64). Median TTF was 12 vs. 2.6 months (
p
= 0.045, MIPI-adjusted HR 0.69; 95%CI 0.47–1.02). Overall and complete response rates were 63 vs. 45% (
p
= 0.049) and 42 vs. 19% (
p
= 0.0062). A significant treatment effect was seen in the subgroup of patients >65 years (aHR 0.48, 0.29–0.79) and without previous ASCT (aHR 0.52, 0.28–0.96). Toxicity was mostly hematological and attributable to the chemotherapeutic backbone. Grade ≥3 leukocytopenia and lymphocytopenia were more common in R-HAD + B without differences in severe infections between both arms. Bortezomib in combination with chemotherapy can be effective in r/r MCL and should be evaluated further as a therapeutic option, especially if therapy with BTK inhibitors is not an option. Trial registration: NCT01449344. |
doi_str_mv | 10.1038/s41375-024-02254-2 |
format | Article |
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n
= 64) or R-HAD (
n
= 64). Median TTF was 12 vs. 2.6 months (
p
= 0.045, MIPI-adjusted HR 0.69; 95%CI 0.47–1.02). Overall and complete response rates were 63 vs. 45% (
p
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p
= 0.0062). A significant treatment effect was seen in the subgroup of patients >65 years (aHR 0.48, 0.29–0.79) and without previous ASCT (aHR 0.52, 0.28–0.96). Toxicity was mostly hematological and attributable to the chemotherapeutic backbone. Grade ≥3 leukocytopenia and lymphocytopenia were more common in R-HAD + B without differences in severe infections between both arms. Bortezomib in combination with chemotherapy can be effective in r/r MCL and should be evaluated further as a therapeutic option, especially if therapy with BTK inhibitors is not an option. 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N.</creatorcontrib><creatorcontrib>Dargel, Beate</creatorcontrib><creatorcontrib>Durot, Eric</creatorcontrib><creatorcontrib>Foussard, Charles</creatorcontrib><creatorcontrib>Silkenstedt, Elisabeth</creatorcontrib><creatorcontrib>Weigert, Oliver</creatorcontrib><creatorcontrib>Pott, Christiane</creatorcontrib><creatorcontrib>Klapper, Wolfram</creatorcontrib><creatorcontrib>Hiddemann, Wolfgang</creatorcontrib><creatorcontrib>Unterhalt, Michael</creatorcontrib><creatorcontrib>Hoster, Eva</creatorcontrib><creatorcontrib>Ribrag, Vincent</creatorcontrib><creatorcontrib>Dreyling, Martin</creatorcontrib><title>The addition of bortezomib to rituximab, high-dose cytarabine and dexamethasone in relapsed or refractory mantle cell lymphoma—a randomized, open-label phase III trial of the European mantle cell lymphoma network</title><title>Leukemia</title><addtitle>Leukemia</addtitle><addtitle>Leukemia</addtitle><description>The therapy of relapsed or refractory (r/r) mantle cell lymphoma (MCL) patients remains a major clinical challenge to date. 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n
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n
= 64). Median TTF was 12 vs. 2.6 months (
p
= 0.045, MIPI-adjusted HR 0.69; 95%CI 0.47–1.02). Overall and complete response rates were 63 vs. 45% (
p
= 0.049) and 42 vs. 19% (
p
= 0.0062). A significant treatment effect was seen in the subgroup of patients >65 years (aHR 0.48, 0.29–0.79) and without previous ASCT (aHR 0.52, 0.28–0.96). Toxicity was mostly hematological and attributable to the chemotherapeutic backbone. Grade ≥3 leukocytopenia and lymphocytopenia were more common in R-HAD + B without differences in severe infections between both arms. Bortezomib in combination with chemotherapy can be effective in r/r MCL and should be evaluated further as a therapeutic option, especially if therapy with BTK inhibitors is not an option. 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We conducted a randomized, open-label, parallel-group phase-III trial hypothesizing superior efficacy of rituximab, high-dose cytarabine and dexamethasone with bortezomib (R-HAD + B) versus without (R-HAD) in r/r MCL ineligible for or relapsed after autologous stem cell transplant (ASCT). Primary endpoint was time to treatment failure (TTF), secondary endpoints included response rates, progression free survival, overall survival, and safety. In total, 128 of 175 planned patients were randomized to R-HAD + B (
n
= 64) or R-HAD (
n
= 64). Median TTF was 12 vs. 2.6 months (
p
= 0.045, MIPI-adjusted HR 0.69; 95%CI 0.47–1.02). Overall and complete response rates were 63 vs. 45% (
p
= 0.049) and 42 vs. 19% (
p
= 0.0062). A significant treatment effect was seen in the subgroup of patients >65 years (aHR 0.48, 0.29–0.79) and without previous ASCT (aHR 0.52, 0.28–0.96). Toxicity was mostly hematological and attributable to the chemotherapeutic backbone. Grade ≥3 leukocytopenia and lymphocytopenia were more common in R-HAD + B without differences in severe infections between both arms. Bortezomib in combination with chemotherapy can be effective in r/r MCL and should be evaluated further as a therapeutic option, especially if therapy with BTK inhibitors is not an option. Trial registration: NCT01449344.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>38678093</pmid><doi>10.1038/s41375-024-02254-2</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-0987-7373</orcidid><orcidid>https://orcid.org/0000-0003-1256-173X</orcidid><orcidid>https://orcid.org/0000-0002-0749-1389</orcidid><orcidid>https://orcid.org/0000-0003-2444-416X</orcidid><orcidid>https://orcid.org/0000-0002-6830-9296</orcidid><orcidid>https://orcid.org/0000-0003-3463-0089</orcidid><orcidid>https://orcid.org/0009-0005-9260-8340</orcidid><orcidid>https://orcid.org/0000-0002-9009-4236</orcidid><orcidid>https://orcid.org/0000-0001-6082-7710</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0887-6924 |
ispartof | Leukemia, 2024-06, Vol.38 (6), p.1307-1314 |
issn | 0887-6924 1476-5551 1476-5551 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11147755 |
source | SpringerLink Journals - AutoHoldings |
subjects | 631/67/1059/602 692/699/1541/1990/291/1621/1915 Bortezomib Cancer Research Chemotherapy Critical Care Medicine Cytarabine Dexamethasone Hematology Immunotherapy Inhibitor drugs Intensive Internal Medicine Labels Leukopenia Lymphoma Lymphopenia Mantle cell lymphoma Medicine Medicine & Public Health Monoclonal antibodies Oncology Patients Response rates Rituximab Stem cell transplantation Stem cells Subgroups Survival Targeted cancer therapy Toxicity |
title | The addition of bortezomib to rituximab, high-dose cytarabine and dexamethasone in relapsed or refractory mantle cell lymphoma—a randomized, open-label phase III trial of the European mantle cell lymphoma network |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T18%3A20%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20addition%20of%20bortezomib%20to%20rituximab,%20high-dose%20cytarabine%20and%20dexamethasone%20in%20relapsed%20or%20refractory%20mantle%20cell%20lymphoma%E2%80%94a%20randomized,%20open-label%20phase%20III%20trial%20of%20the%20European%20mantle%20cell%20lymphoma%20network&rft.jtitle=Leukemia&rft.au=Fischer,%20Luca&rft.date=2024-06-01&rft.volume=38&rft.issue=6&rft.spage=1307&rft.epage=1314&rft.pages=1307-1314&rft.issn=0887-6924&rft.eissn=1476-5551&rft_id=info:doi/10.1038/s41375-024-02254-2&rft_dat=%3Cproquest_pubme%3E3047943502%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3063932027&rft_id=info:pmid/38678093&rfr_iscdi=true |