Aw Andrew, Brown Jennifer R
a Department of Medicine, Division of Hematology , The Ottawa Hospital, University of Ottawa , Ottawa , Canada.
b CLL Center, Department of Medical Oncology , Dana-Farber Cancer Institute , Boston , MA , USA.
Leuk Lymphoma. 2017 Oct;58(10):2287-2297. doi: 10.1080/10428194.2017.1312387. Epub 2017 May 9.
The recent development of small molecule inhibitors targeted at the B-cell receptor (BCR) pathway and the anti-apoptotic protein BCL-2 has revolutionized the care of patients with chronic lymphocytic leukemia (CLL). While durable responses to the BCR inhibitor ibrutinib have been observed in both previously untreated and relapsed/refractory CLL patients, residual disease is common in patients treated with single-agent ibrutinib. Interest remains high in therapeutic combinations that may lead to better quality remissions. A potential partner to ibrutinib with a distinct mechanism of action that is likely to lead to deeper responses is the BCL-2 inhibitor venetoclax. Preclinical studies have suggested synergism between inhibitors of BCR and BCL-2 and have paved the way to the development of ongoing clinical trials aimed at evaluating the combination of ibrutinib with venetoclax in CLL patients.
针对B细胞受体(BCR)通路和抗凋亡蛋白BCL-2的小分子抑制剂的最新进展,彻底改变了慢性淋巴细胞白血病(CLL)患者的治疗方式。虽然在既往未治疗和复发/难治性CLL患者中均观察到对BCR抑制剂伊布替尼的持久反应,但在接受单药伊布替尼治疗的患者中,残留疾病很常见。对于可能带来更好缓解质量的治疗组合,人们的兴趣依然浓厚。BCL-2抑制剂维奈克拉是伊布替尼的一个潜在伙伴,其作用机制独特,可能带来更深度的反应。临床前研究表明BCR抑制剂与BCL-2抑制剂之间存在协同作用,为开展旨在评估伊布替尼与维奈克拉联合治疗CLL患者的临床试验铺平了道路。