Division of Oncology, University Hospital Zürich, Rämistrasse 100 8091 Zürich, Switzerland.
Haematologica. 2012 Jul;97(7):1085-91. doi: 10.3324/haematol.2011.053173. Epub 2012 Feb 7.
Mantle cell lymphoma accounts for 6% of all B-cell lymphomas and is generally incurable. It is characterized by the translocation t(11;14) leading to cyclin D1 over-expression. Cyclin D1 is downstream of the mammalian target of rapamycin threonine kinase and can be effectively blocked by mammalian target of rapamycin inhibitors. We set out to examine the single agent activity of the orally available mammalian target of rapamycin inhibitor everolimus in a prospective, multicenter trial in patients with relapsed or refractory mantle cell lymphoma (NCT00516412).
Eligible patients who had received a maximum of three prior lines of chemotherapy were given everolimus 10 mg for 28 days (one cycle) for a total of six cycles or until disease progression. The primary endpoint was the best objective response. Adverse reactions, progression-free survival and molecular response were secondary endpoints.
Thirty-six patients (35 evaluable) were enrolled and treatment was generally well tolerated with Common Terminology Criteria grade ≥ 3 adverse events (>5%) including anemia (11%), thrombocytopenia (11%) and neutropenia (8%). The overall response rate was 20% (95% CI: 8-37%) with two complete remissions and five partial responses; 49% of the patients had stable disease. At a median follow-up of 6 months, the median progression-free survival was 5.5 months (95% CI: 2.8-8.2) overall and 17.0 (6.4-23.3) months for 18 patients who received six or more cycles of treatment. Three patients achieved a lasting complete molecular response, as assessed by polymerase chain reaction analysis of peripheral blood.
Everolimus as a single agent is well tolerated and has anti-lymphoma activity in relapsed or refractory mantle cell lymphoma. Further studies of everolimus in combination with chemotherapy or as a single agent for maintenance treatment are warranted.
套细胞淋巴瘤占所有 B 细胞淋巴瘤的 6%,通常无法治愈。其特征在于易位 t(11;14)导致 cyclin D1 过表达。cyclin D1 是哺乳动物雷帕霉素靶蛋白丝氨酸/苏氨酸激酶的下游分子,可以被哺乳动物雷帕霉素抑制剂有效地阻断。我们旨在研究口服哺乳动物雷帕霉素抑制剂依维莫司在复发或难治性套细胞淋巴瘤患者中的单药活性(NCT00516412)。
入组的患者既往接受过最大 3 线化疗,给予依维莫司 10mg,28 天为一个周期(共 6 个周期),直至疾病进展。主要终点是最佳客观缓解。不良反应、无进展生存期和分子缓解是次要终点。
36 例患者(35 例可评估)入组,治疗总体耐受性良好,常见不良事件≥3 级(>5%)包括贫血(11%)、血小板减少(11%)和中性粒细胞减少(8%)。总缓解率为 20%(95%CI:8-37%),完全缓解 2 例,部分缓解 5 例;49%的患者疾病稳定。中位随访 6 个月时,总无进展生存期为 5.5 个月(95%CI:2.8-8.2),接受 6 个或更多周期治疗的 18 例患者中位无进展生存期为 17.0 个月(6.4-23.3)。3 例患者通过外周血聚合酶链反应分析达到持久的完全分子缓解。
依维莫司单药治疗复发或难治性套细胞淋巴瘤耐受性良好,具有抗淋巴瘤活性。需要进一步研究依维莫司联合化疗或作为单药维持治疗。