R2-based frontline FL: FLIPI24 flags high-risk patients with lower CR30 and 5-year PFS
- Trial ID
- NCT00695786 on ClinicalTrials.gov
- Cancer type
- Follicular Lymphoma (FL)
- Related trial IDs
- NCT02532257NCT02871219
- Published in
- New in Oncology - Aug 6, 2026
FLIPI24 (a prognostic model for newly diagnosed follicular lymphoma) was evaluated in a pooled MD Anderson cohort of first-line, “chemo-free” immunotherapy regimens built around CD20 antibodies plus the immunomodulatory agent lenalidomide: rituximab+lenalidomide (R2; NCT00695786; n=79), ibrutinib (BTK inhibitor)+R2 (NCT02532257; n=38), and obinutuzumab (type II anti-CD20)+lenalidomide (NCT02871219; n=90), totaling 207 patients. Risk groups were 48% low, 39% intermediate, and 13% high; end-of-induction CR was similar (91% vs 90% vs 83%), but high-risk patients had lower CR at 30 months (CR30 59% vs 79% vs 84%; p=0.044) and worse PFS (5-year PFS 58% vs 79% vs 79%; p=0.049) after median 9.1 years’ follow-up, with no OS separation reported. In context, frontline R2 in the randomized Phase 3 RELEVANCE trial delivered broadly comparable long-term disease control to rituximab-chemotherapy (e.g., ~60% PFS at 6 years in both arms), so a 5-year PFS of 58% in FLIPI24 high-risk looks “SOC-range” overall—but FLIPI24 still meaningfully enriches for patients more likely to relapse despite modern R2-based therapy.
Take home
If FLIPI24 can be operationalized prospectively, it looks like a practical way to identify the ~10–15% “high-risk despite R2” group for intensified/novel strategies (or closer MRD-driven surveillance), because the early CR rate alone clearly doesn’t tell you who will stay in durable remission.
Source: Read the original publication
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