a Division of Hematology , The Ohio State University Comprehensive Cancer Center , Columbus , OH , USA.
b Department of Hematology/Oncology, The University of Chicago Medicine , Chicago , IL , USA.
Leuk Lymphoma. 2019 Aug;60(8):1972-1977. doi: 10.1080/10428194.2018.1562180. Epub 2019 Jan 11.
Entospletinib (GS-9973), an oral, selective inhibitor of spleen tyrosine kinase (SYK), was evaluated as monotherapy in this multicenter, phase 2 study (NCT01799889) of 49 patients with relapsed or refractory chronic lymphocytic leukemia (CLL), including those with Richter's transformation (RT), who had received prior therapy with a B-cell receptor (BCR) inhibitor. Patients were treated with entospletinib 400 mg BID as the starting dose. Sixteen patients achieved partial response and 21 had stable disease. The overall response rate was 32.7% (95% confidence interval [CI]: 21.7-45.3%). The median progression-free survival (PFS) was 5.6 (95% CI: 3.7-8.3) months. Twenty-one (of 43) patients (48.8%) experienced nodal response. Adverse events (AEs) occurred in all patients; most commonly fatigue, diarrhea, and anemia. Entospletinib monotherapy has clinical activity for patients with CLL and RT who have relapsed following therapy with BCR inhibitors.
依鲁替尼(GS-9973)是一种口服、选择性脾酪氨酸激酶(SYK)抑制剂,在这项多中心、2 期研究(NCT01799889)中作为单药治疗,共纳入 49 例复发或难治性慢性淋巴细胞白血病(CLL)患者,包括伴有Richter 转化(RT)的患者,这些患者之前接受过 B 细胞受体(BCR)抑制剂治疗。患者起始剂量为依鲁替尼 400mg,bid。16 例患者达到部分缓解,21 例患者病情稳定。总缓解率为 32.7%(95%置信区间[CI]:21.7-45.3%)。中位无进展生存期(PFS)为 5.6 个月(95%CI:3.7-8.3)。21 例(43 例中的 21 例)患者(48.8%)出现淋巴结反应。所有患者均发生不良事件(AE);最常见的是疲劳、腹泻和贫血。依鲁替尼单药治疗对接受 BCR 抑制剂治疗后复发的 CLL 和 RT 患者具有临床活性。