The LEVERAGE trial was a three-drug biologic triplet being used in patients with treatment-naive follicular lymphoma. So we included 50 patients with GELF-positive FL and the treatment combination was fixed-duration obinutuzumab, lenalidomide, and venetoclax, so non-chemotherapy triplet. I think the take-home is that the regimen was active, the complete metabolic response rate after six cycles of therapy was 86%, which is pretty encouraging and comparable, if not better, to chemoimmunotherapy...
The LEVERAGE trial was a three-drug biologic triplet being used in patients with treatment-naive follicular lymphoma. So we included 50 patients with GELF-positive FL and the treatment combination was fixed-duration obinutuzumab, lenalidomide, and venetoclax, so non-chemotherapy triplet. I think the take-home is that the regimen was active, the complete metabolic response rate after six cycles of therapy was 86%, which is pretty encouraging and comparable, if not better, to chemoimmunotherapy. We did have obinutuzumab maintenance after that for responders, and we had a two-year PFS of around 92%, which I think is better than historic control of chemoimmunotherapy. We did see a little bit of hematologic toxicity though, and a few patients had to discontinue early. So that was one of the things that we observed is unsurprisingly from the combination of lenalidomide and venetoclax and obinutuzumab, we saw neutropenia, but it was manageable. And so patients did generally quite well. So encouraging data. We’re planning to look at that in some more detail with some more in-depth molecular analyses, including dynamic changes in ctDNA at future conferences.
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