https://doi.org/10.55788/af215ace
The phase 1/2 study (NCT02500407) recently demonstrated high complete response (CR) rates with the CD20/CD3 T-cell engaging bispecific antibody mosunetuzumab among patients with RR FL [1]. Dr Sarit Assouline (Jewish General Hospital, Canada) presented the current subgroup analysis of this study after 3 years of follow-up [2]. All participants received mosunetuzumab in the third line or later and progression of disease within 24 months (POD24) was observed in 52% of participants.
After 3 years of therapy, CR was seen in 60% of participants with POD24, a figure consistent with the overall study population (also 60%). Similarly, CR rates in participants older than 64 years (67%) and those who received mosunetuzumab as fourth-line therapy or later (55%) were comparable with the general trial population. In addition, the median duration of CR was not reached in participants with POD24 or older participants but was 33 months in ‘fourth-line-or-higher’ participants. The 3-year progression-free survival rates were 44% in the POD24 subgroup, 47% in participants over 64 years, and 43% in the overall population. In fourth-line-or-higher participants, this rate appeared lower at 36% compared with third-line participants (54%).
The safety profile of mosunetuzumab was manageable and consistent across subgroups. The observed adverse events were cytokine release syndrome (44%), neutropenia (29%), and serious infections (20%).
“The consistent results of mosunetuzumab across subgroups of participants with RR FL and the manageable safety profile support outpatient administration of this agent,” concluded Dr Assouline.
- Budde LE, et al. Lancet Oncol. 2022;23(8):1055–1065.
- Assouline S, et al. Mosunetuzumab demonstrates clinically meaningful outcomes in high-risk patients with heavily pre-treated R/R FL after ≥3 years of follow-up: subgroup analysis of a pivotal phase 2 study. S233, EHA congress 2024, 13–16 June, Madrid, Spain.
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