Department of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, California.
Department of Pediatrics - Hematology/Oncology, Stanford University, Palo Alto, California.
Cancer Discov. 2021 Jun;11(6):1440-1453. doi: 10.1158/2159-8290.CD-20-1465. Epub 2021 Feb 16.
Combining venetoclax, a selective BCL2 inhibitor, with low-dose navitoclax, a BCL-X/BCL2 inhibitor, may allow targeting of both BCL2 and BCL-X without dose-limiting thrombocytopenia associated with navitoclax monotherapy. The safety and preliminary efficacy of venetoclax with low-dose navitoclax and chemotherapy was assessed in this phase I dose-escalation study (NCT03181126) in pediatric and adult patients with relapsed/refractory (R/R) acute lymphoblastic leukemia or lymphoblastic lymphoma. Forty-seven patients received treatment. A recommended phase II dose of 50 mg navitoclax for adults and 25 mg for patients <45 kg with 400 mg adult-equivalent venetoclax was identified. Delayed hematopoietic recovery was the primary safety finding. The complete remission rate was 60%, including responses in patients who had previously received hematopoietic cell transplantation or immunotherapy. Thirteen patients (28%) proceeded to transplantation or CAR T-cell therapy on study. Venetoclax with navitoclax and chemotherapy was well tolerated and had promising efficacy in this heavily pretreated patient population. SIGNIFICANCE: In this phase I study, venetoclax with low-dose navitoclax and chemotherapy was well tolerated and had promising efficacy in patients with relapsed/refractory acute lymphoblastic leukemia or lymphoblastic lymphoma. Responses were observed in patients across histologic and genomic subtypes and in those who failed available therapies including stem cell transplant...
联合使用选择性 BCL2 抑制剂 venetoclax 和低剂量 navitoclax(BCL-X/BCL2 抑制剂),可能可以靶向 BCL2 和 BCL-X,而不会出现 navitoclax 单药治疗相关的剂量限制血小板减少症。本研究采用 Venetoclax 联合低剂量 navitoclax 和化疗治疗复发/难治性(R/R)急性淋巴细胞白血病或淋巴母细胞淋巴瘤的安全性和初步疗效,为 I 期剂量递增研究(NCT03181126)。47 例患者接受了治疗。确定了成人 50mg 纳维妥昔单抗和<45kg 患者 25mg 的推荐 II 期剂量,联合 400mg 成人等效剂量的 venetoclax。主要安全性发现为造血恢复延迟。完全缓解率为 60%,包括先前接受过造血细胞移植或免疫治疗的患者的缓解。13 例患者(28%)在研究中进行了移植或 CAR-T 细胞治疗。Venetoclax 联合 navitoclax 和化疗耐受性良好,在既往接受过多线治疗的患者中具有良好的疗效。意义:在这项 I 期研究中,venetoclax 联合低剂量 navitoclax 和化疗在复发/难治性急性淋巴细胞白血病或淋巴母细胞淋巴瘤患者中具有良好的耐受性和疗效。在组织学和基因组亚型以及接受过包括干细胞移植在内的现有治疗方案失败的患者中观察到了缓解。