Department of Hematology, Pukou CLL Center, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Collaborative Innovation Center for Cancer Personalized Medicine, Nanjing, People's Republic of China.
Department of Hematology, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou, People's Republic of China.
Am J Hematol. 2023 Apr;98(4):571-579. doi: 10.1002/ajh.26826. Epub 2023 Jan 22.
Orelabrutinib is a novel, small molecule, selective irreversible Bruton's tyrosine kinase inhibitor. The aim of this study was to evaluate the efficacy and safety in patients with refractory or relapsed chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL). This is single-arm, multi-center, open-label, phase 2 study in 80 eligible Chinese patients, who were treated with monotherapy of orelabrutinib at 150 mg once daily. Overall response rate evaluated by an independent review committee was the primary endpoint, and secondary endpoints include progression-free survival, overall survival, and safety. Independent review committee assessed overall response rate was 92.5% (74/80); complete response 21.3% (17/80), partial response 60.0% (48/80), partial response with lymphocytosis 11.3% (9/80). At a 32.3-month median follow-up, the median progression-free survival had not been achieved, while the 30-month progression-free survival rate and overall survival rates were 70.9% (95% confidence interval [CI], 59.5-79.6) and 81.3% (95% CI, 70.8-88.2), respectively. Orelabrutinib also revealed substantial response in patients with high prognostic risks: overall response rates of patients carrying positive TP53 mutational status or del(17p), del(11q), as well as unmutated immunoglobulin heavy-chain variable region gene were 100%, 94.7%, and 93.9%, respectively. Most adverse events were in low grade, with 86.8% of AEs being Grade 1 or 2. Nearly 67% of patients were still receiving orelabrutinib after almost a 3-year follow-up. In conclusion, Orelabrutinib demonstrated compelling efficacy as well as safety profiles, with a noteworthy number of patients obtaining complete response in refractory or relapsed CLL/SLL.
奥雷巴替尼是一种新型、小分子、选择性、不可逆布鲁顿酪氨酸激酶抑制剂。本研究旨在评估其在难治/复发慢性淋巴细胞白血病(CLL)/小淋巴细胞淋巴瘤(SLL)患者中的疗效和安全性。这是一项在中国 80 例合格患者中开展的单臂、多中心、开放标签、2 期研究,患者接受奥雷巴替尼 150mg 每日一次单药治疗。独立评审委员会评估的总缓解率为主要终点,次要终点包括无进展生存期、总生存期和安全性。独立评审委员会评估的总缓解率为 92.5%(74/80);完全缓解率为 21.3%(17/80),部分缓解率为 60.0%(48/80),伴有淋巴细胞增多的部分缓解率为 11.3%(9/80)。在中位随访 32.3 个月时,中位无进展生存期尚未达到,而 30 个月无进展生存率和总生存率分别为 70.9%(95%可信区间[CI],59.5-79.6)和 81.3%(95%CI,70.8-88.2)。奥雷巴替尼在高预后风险患者中也显示出显著的疗效:携带 TP53 突变状态或 del(17p)、del(11q)以及未突变免疫球蛋白重链可变区基因的患者的总缓解率分别为 100%、94.7%和 93.9%。大多数不良反应为低级别,86.8%的不良反应为 1 级或 2 级。在近 3 年的随访后,近 67%的患者仍在接受奥雷巴替尼治疗。总之,奥雷巴替尼具有良好的疗效和安全性,在难治/复发 CLL/SLL 患者中,相当比例的患者获得完全缓解。