First-line Ibr + Ven is an all-oral, once-daily, chemotherapy-free regimen that continues to provide deep, durable clinical responses in pts with CLL.
With additional follow-up in pts with confirmed uMRD after Ibr + Ven, 4-y OS rates were ≥98% and 4-y PFS rates were ≥88% in pts randomly assigned to fixed duration or continued Ibrutinib.
The durability of uMRD and the 3-y disease free survival rate of 85% without ongoing treatment are encouraging and support the promising potential for treatment-free remission.
Together with the safety data, these results demonstrate a favorable benefit-risk profile with fixed duration Ibr + Ven.
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Jackie