Section of Hematology, Department of Medicine, University of Verona, 37134 Verona, Italy.
B-Cell Neoplasia Unit, Division of Experimental Oncology, Università Vita-Salute San Raffaele, 20132 Milan, Italy.
Curr Oncol. 2022 Apr 15;29(4):2792-2797. doi: 10.3390/curroncol29040227.
Patients with chronic lymphocytic leukemia (CLL) relapsing on ibrutinib are often treated with the Bcl-2 inhibitor venetoclax. However, the transition from one agent to another poses some clinical challenges due to disease flares sometimes occurring right after ibrutinib interruption. Here, we describe three clinical vignettes highlighting two distinct patterns of ibrutinib-to-venetoclax transition. While patients following the favorable pattern transited to venetoclax without experiencing disease flare, the one patient who took the unfavorable path showed rapid disease rebound, with large-cell transformation occurring one week after ibrutinib interruption. A high burden of and mutations was found only in patients with the favorable transition pattern, suggesting that removing BTK inhibition might be particularly harmful if CLL cells are progressing through mechanisms external to the BTK axis.
慢性淋巴细胞白血病 (CLL) 患者在伊布替尼复发后,常采用 Bcl-2 抑制剂维奈托克进行治疗。然而,由于伊布替尼中断后有时会立即出现疾病爆发,因此从一种药物转换为另一种药物会带来一些临床挑战。在此,我们描述了三个临床病例,突出了伊布替尼到维奈托克转换的两种不同模式。在没有发生疾病爆发的情况下,遵循有利模式的患者顺利转换为维奈托克,而采取不利模式的患者则表现出快速的疾病反弹,伊布替尼中断后一周即发生大细胞转化。仅在具有有利转换模式的患者中发现了 和 突变的高负担,这表明如果 CLL 细胞通过 BTK 轴以外的机制进展,那么去除 BTK 抑制可能特别有害。