Division of Neuro-Oncology, Department of Neurology and Neurological Surgery, Fred Hutchinson Cancer Research Center, Seattle Cancer Care Alliance, University of Washington, 825 Eastlake Ave E, MS: G4-940, Seattle, WA, 98109, USA,
J Neurooncol. 2014 May;118(1):155-62. doi: 10.1007/s11060-014-1411-8. Epub 2014 Mar 1.
There is comparatively limited therapy for recurrent primary central nervous system lymphoma (PCNSL). Salvage therapies include re-challenge with high-dose methotrexate (HD-MTX), whole brain radiotherapy, temozolomide, topotecan and premetrexed. Bendamustine is a novel bifunctional alkylator with established activity in B cell systemic lymphomas but never previously evaluated in PCNSL. The objective of the current study was to assess response and toxicity of bendamustine in recurrent PCNSL following prior salvage therapy in a retrospective case series. Twelve adults [six males; six females: median age 59 years (range 43-74)] with HD-MTX refractory recurrent PCNSL were treated with bendamustine. All patients were treated at second recurrence following failure of prior salvage therapy. A cycle of bendamustine was defined as two consecutive days of treatment (100 mg/m(2)/day) administered once every 4 weeks (maximum number of cycles 6). Toxicities seen were Grade 2 (24 episodes in 10 patients) and 3 (10 episodes in 5 patients) only and included lymphopenia (8 patients), hyperglycemia (7 patients), fatigue (7 patients) and nausea (4 patients). The median number of cycles of therapy was 3.5 (range 1-6). Radiographic response was progressive disease in 5 (42%), stable disease in 1 (8%), partial response in 3 (25%) and complete response in 3 (25%). Median progression free survival (PFS) was 3.5 months (range 1-14 months) and 6-month PFS was 33 %. In this small retrospective series of select patients with recurrent PCNSL refractory to HD-MTX, bendamustine appears to have modest single agent activity with manageable toxicity. Confirmation in a larger series of similar patients is required.
原发性中枢神经系统淋巴瘤(PCNSL)的复发治疗方法相对有限。挽救治疗包括高剂量甲氨蝶呤(HD-MTX)再挑战、全脑放疗、替莫唑胺、拓扑替康和培美曲塞。苯达莫司汀是一种新型双功能烷化剂,在 B 细胞全身淋巴瘤中具有明确的活性,但从未在 PCNSL 中进行过评估。本研究的目的是在回顾性病例系列中评估苯达莫司汀在先前挽救治疗后复发的 PCNSL 中的疗效和毒性。12 例[6 例男性;6 例女性:中位年龄 59 岁(范围 43-74 岁)]接受 HD-MTX 难治性复发 PCNSL 的患者接受了苯达莫司汀治疗。所有患者均在先前挽救治疗失败后第二次复发时接受治疗。一个苯达莫司汀周期定义为连续 2 天治疗(每天 100mg/m2),每 4 周 1 次(最多 6 个周期)。观察到的毒性为 2 级(10 例中有 24 例)和 3 级(5 例中有 10 例),包括淋巴细胞减少症(8 例)、高血糖症(7 例)、疲劳(7 例)和恶心(4 例)。治疗周期的中位数为 3.5 个周期(范围 1-6 个周期)。影像学反应为进展性疾病 5 例(42%)、稳定疾病 1 例(8%)、部分缓解 3 例(25%)和完全缓解 3 例(25%)。无进展生存期(PFS)的中位数为 3.5 个月(范围 1-14 个月),6 个月 PFS 为 33%。在这项针对难治性 HD-MTX 复发 PCNSL 的精选患者的小型回顾性系列研究中,苯达莫司汀似乎具有适度的单药活性,毒性可管理。需要在类似的更大系列患者中进行确认。