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.
Luca FischerLinmiao JiangJan DürigChristian SchmidtStephan StilgenbauerKrimo BouabdallahPhilippe Solal-CelignyChristian W ScholzPierre FeugierMaike de WitRalf Ulrich TrappeMichael HallekUllrich GraevenMathias HänelMartin HoffmannVincent DelwailMargaret MacroJochen GreinerAristoteles A N GiagounidisBeate DargelEric DurotCharles FoussardElisabeth SilkenstedtOliver WeigertChristiane PottWolfram KlapperWolfgang HiddemannMichael UnterhaltEva HosterVincent RibragMartin DreylingPublished in: Leukemia (2024)
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.
Keyphrases
- phase iii
- open label
- high dose
- phase ii
- clinical trial
- newly diagnosed
- end stage renal disease
- double blind
- multiple myeloma
- acute myeloid leukemia
- stem cells
- placebo controlled
- low dose
- chronic kidney disease
- diffuse large b cell lymphoma
- study protocol
- ejection fraction
- acute lymphoblastic leukemia
- prognostic factors
- free survival
- phase ii study
- squamous cell carcinoma
- randomized controlled trial
- stem cell transplantation
- patient reported outcomes
- mesenchymal stem cells
- bone marrow
- tyrosine kinase
- early onset
- cell therapy
- locally advanced
- patient reported
- radiation therapy