This is an open-label, multicenter, phase II study to evaluate the safety and efficacy following an oral daily administration of orelabrutinib....A total of 80 patients with r/r CLL/SLL were enrolled....The ORR was 100% in patients with Del(17p) and/or TP53 mutation....The ORR was 94.7% for Del(11q)) and 93.9% for unmutated IGHV....Orelabrutinib provides a favorable therapeutic choice for patients with r/r CLL/SLL.