Department of Neurology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Leuk Lymphoma. 2023 Sep;64(9):1545-1553. doi: 10.1080/10428194.2023.2223734. Epub 2023 Jun 15.
Central Nervous System (CNS) Lymphomas are aggressive brain tumors with limited treatment options. Targeting the phosphoinositide 3-kinase (PI3K) pathway yields promising responses across B-cell malignancies, but its therapeutic potential in CNS lymphomas remains unexplored. We present pre-clinical and clinical data on the pan-PI3K inhibitor Buparlisib in CNS lymphomas. In a primary CNS lymphoma-patient-derived cell line, we define the EC50. Four patients with recurrent CNS lymphoma were enrolled in a prospective trial. We evaluated Buparlisib plasma and cerebrospinal fluid pharmacokinetics, clinical outcomes, and adverse events. Treatment was well tolerated. Common toxicities include hyperglycemia, thrombocytopenia, and lymphopenia. The presence of Buparlisib in plasma and CSF was confirmed 2h post-treatment with a median CSF concentration below the EC50 defined in the cell line All four patients were evaluated for response and the median time to progression was 39 days. Buparlisib monotherapy did not lead to meaningful responses and the trial was prematurely stopped. NCT02301364.
中枢神经系统(CNS)淋巴瘤是侵袭性脑肿瘤,治疗选择有限。针对磷酸肌醇 3-激酶(PI3K)通路的靶向治疗在 B 细胞恶性肿瘤中取得了有希望的反应,但在 CNS 淋巴瘤中的治疗潜力仍未得到探索。我们提出了关于中枢神经系统淋巴瘤中 pan-PI3K 抑制剂 Buparlisib 的临床前和临床数据。在原发性中枢神经系统淋巴瘤患者来源的细胞系中,我们确定了 EC50。有 4 名复发性中枢神经系统淋巴瘤患者入组了一项前瞻性试验。我们评估了 Buparlisib 的血浆和脑脊液药代动力学、临床结局和不良事件。治疗耐受性良好。常见的毒性包括高血糖、血小板减少和淋巴细胞减少。治疗后 2 小时即可在血浆和 CSF 中检测到 Buparlisib,脑脊液中的浓度中位数低于细胞系中定义的 EC50。所有 4 名患者均进行了反应评估,中位无进展生存期为 39 天。Buparlisib 单药治疗并未导致有意义的反应,因此该试验提前终止。NCT02301364。