4.7 Article

Ofatumumab plus HyperCVAD/HD-MA induction leads to high rates of minimal residual disease negativity in patients with newly diagnosed mantle cell lymphoma, results of a phase 2 study

Journal

CANCER
Volume 128, Issue 8, Pages 1595-1604

Publisher

WILEY
DOI: 10.1002/cncr.34106

Keywords

CD20; MIPI score; monoclonal antibody; p53; survival outcomes

Categories

Funding

  1. Roswell Park Comprehensive Cancer Center and its Biostatistics Shared Resource
  2. National Comprehensive Cancer Network Oncology Research Program by Novartis
  3. Roswell Park Cancer Institute and its Biostatistics Shared Resource
  4. National Cancer Institute [P30CA016056]

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This study evaluates the safety and efficacy of combining ofatumumab with HyperCVAD/MA in newly diagnosed MCL. The results show that this combination therapy leads to high rates of MRD negativity and improved overall survival in patients with MCL. Achieving a CR post-induction by both imaging and flow cytometry is associated with better outcomes.
Background Ofatumumab is a humanized type 1 anti-CD20 monoclonal antibody. Preclinical studies show improved complement-mediated cytotoxicity (CMC) compared to rituximab in mantle cell lymphoma (MCL). This study evaluates the safety and efficacy of combining ofatumumab with HyperCVAD/MA (O-HyperCVAD) in newly diagnosed MCL. Methods In this single-arm phase 2 study, 37 patients were treated with the combination of O-HyperCVAD for 4 or 6 cycles, followed by high dose chemotherapy and autologous stem cell transplant. Primary objectives were overall response rate (ORR) and complete response (CR) rate at the end of therapy. Secondary objectives included minimal residual disease (MRD) negativity, progression-free survival (PFS), and overall survival (OS). Results Median age was 60 years; ORR was 86% and 73% achieved a CR by modified Cheson criteria. The MRD negativity rate was 78% after 2 cycles of therapy, increasing to 96% at the end of induction; median PFS and OS were 45.5 months and 56 months, respectively. Achieving a post-induction CR by both imaging and flow cytometry was associated with improved PFS and OS. Early MRD negativity (post-2 cycles) was also associated with an improved PFS but not OS. There were 3 deaths while on therapy, and grades 3 and 4 adverse events (AEs) were observed in 22% and 68% of the patients. Conclusion The addition of ofatumumab to HyperCVAD/HD-MA led to high rates of MRD negativity by flow cytometry in patients with newly diagnosed MCL. Achieving a CR post-induction by both imaging and flow cytometry is associated with improved overall survival.

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