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

Author:

Fischer LucaORCID,Jiang LinmiaoORCID,Dürig Jan,Schmidt Christian,Stilgenbauer StephanORCID,Bouabdallah Krimo,Solal-Celigny Philippe,Scholz Christian W.,Feugier Pierre,de Wit Maike,Trappe Ralf Ulrich,Hallek Michael,Graeven UllrichORCID,Hänel Mathias,Hoffmann Martin,Delwail Vincent,Macro Margaret,Greiner JochenORCID,Giagounidis Aristoteles A. N.,Dargel Beate,Durot EricORCID,Foussard Charles,Silkenstedt Elisabeth,Weigert OliverORCID,Pott ChristianeORCID,Klapper Wolfram,Hiddemann Wolfgang,Unterhalt Michael,Hoster EvaORCID,Ribrag Vincent,Dreyling Martin

Abstract

AbstractThe 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.

Funder

Janssen Pharmaceuticals

Roche

Bristol-Myers Squibb Company | Bristol-Myers Squibb Canada

AstraZeneca

Gilead Sciences

AbbVie

Amgen

Bristol-Myers Squibb

Celgene

GlaxoSmithKline

Eli Lilly and Company

Novartis

Acerta, BeiGene, Sunesis

Merck & Co., Inc. | MSD K.K.

Miltenyi Biotec

Takeda Pharmaceutical Company

Falk Foundation

Pfizer

Sanofi | Sanofi-Aventis Korea Company

Servier

Bayer

Publisher

Springer Science and Business Media LLC

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