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February 8, 2026Blood Advances2 citationsOpen Access

Mosunetuzumab monotherapy is active and tolerable in patients with relapsed/refractory Richter's transformation.

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KLKatharine L. LewisSASarit E. AssoulineRBRoss Ian Baker

Key Points

  • This study aims to evaluate the efficacy and safety of mosunetuzumab in patients with relapsed/refractory Richter's transformation.
  • Investigated 20 patients with relapsed/refractory Richter's transformation
  • Monotherapy with mosunetuzumab was administered
  • Adverse events and cytokine release syndrome were monitored
  • Measured overall response and complete response rates
  • Assessed progression-free and overall survival rates
  • Overall response rate of 40% with mosunetuzumab
  • Complete response rate of 20%, with some durable responses exceeding 20 months
  • Cytokine release syndrome occurred in 65%, mainly of low severity
  • Median progression-free survival was 3.4 months
  • Median overall survival was 10.2 months

Abstract

Richter's transformation (RT) to diffuse large B-cell lymphoma (DLBCL) is an aggressive lymphoma arising from underlying chronic lymphocytic leukaemia (CLL) or small lymphocytic lymphoma (SLL). RT is often chemorefractory, with resultant poor clinical outcomes with standard chemoimmunotherapy. Mosunetuzumab, a bispecific CD20/CD3 T-cell engaging antibody, was investigated in a cohort of 20 patients with relapsed/refractory RT. Cytokine release syndrome (CRS) occurred in 65%, almost exclusively grade 1 (20%) or 2 (40%) and occurring during the first treatment cycle. Other adverse events included infections, neutropenia, thrombocytopenia, tumor flare and low grade neurotoxicity, with no adverse events leading to treatment discontinuation. Mosunetuzumab resulted in an overall response rate (ORR) 40% and complete response rate (CR) 20%. CRs were durable, with 2 patients experiencing CR 20 months without further therapy, and 2 able to proceed to allogeneic stem cell transplant in CR, with no subsequent relapse. Median progression free and overall survival (PFS and OS) was 3.4 and 10.2 months respectively. Given the favorable toxicity profile of mosunetuzumab, and rapid and durable complete responses observed in this cohort, further investigation of mosunetuzumab for the treatment of RT, as monotherapy and in combination with other novel agents or chemotherapy, is warranted. NCT02500407

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Cite This Study

Lewis et al. (2026) studied this question.

synapsesocial.com/papers/6988290a0fc35cd7a8849029https://doi.org/10.1182/bloodadvances.2025017914
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