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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