NOTE

glofitamab

Obinutuzumab + Glofitamab, Complete response: 39% (95% CI, 32 to 48); 63% cytokine release syndrome, 62% grade 3 or higher adverse events.

follow STARGLO

Glofitamab in Relapsed or Refractory Diffuse Large B-Cell Lymphoma

Information

  • Design: Phase 2 study
  • Number of patients: 155
  • Patients characteristics: Patients with relapsed or refractory diffuse large B-cell lymphoma who had received at least two lines of therapy previously
  • Agent: Glofitamab, a bispecific antibody that recruits T cells to tumor cells
  • Treatment line: Third-line therapy or later
  • Trial Name or NCT Number: Not provided (ClinicalTrials.gov number not specified)

Results

  • Primary endpoint: Complete response rate
  • Complete response rate: 39% (95% CI, 32 to 48)
  • Median time to complete response: 42 days (95% CI, 42 to 44)
  • Duration of response: 78% of complete responses were ongoing at 12 months
  • Progression-free survival: 37% (95% CI, 28 to 46) at 12 months

Other findings

  • Adverse events: 63% of patients experienced cytokine release syndrome, and 62% experienced adverse events of grade 3 or higher
  • Discontinuation due to adverse events: 9% of patients

Summary The study demonstrates that glofitamab therapy is effective in patients with relapsed or refractory diffuse large B-cell lymphoma, with a complete response rate of 39%. However, more than half of the patients experienced adverse events of grade 3 or higher, including cytokine release syndrome.