However, we observed a borderline significant effect of more complex genetic alterations as shown by a surrogate of two or more mutations found in our eight-gene panel (median PFS 39.1 months (95% CI 26.0–52.2) vs 70.5 (95% CI 53.2–87.3) p = 0·051; HR 3.35 (95% CI 1.00–0.07) Fig. 2 e).
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Fludarabine and rituximab with escalating doses of lenalidomide followed by lenalidomide/rituximab maintenance in previously untreated chronic lymphocytic leukaemia (CLL): the REVLIRIT CLL-5 AGMT phase I/II study.
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