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Prolonged myelosuppression with clofarabine in the treatment of patients with relapsed or refractory aggressive non-Hodgkin lymphoma

机译:氯法拉滨长期抑制骨髓抑制治疗复发性或难治性侵袭性非霍奇金淋巴瘤患者

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摘要

We evaluated the safety and efficacy of the purine nucleoside analogue, clofarabine, in patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) and mantle cell lymphoma (MCL). Six patients with DLBCL (n = 5) or MCL (n = 1) and a median age of 68 years were treated with 40 mg/m2 clofarabine IV over 2 h for 5 days, repeated every 28 days, for 1–2 cycles. The overall response rate was 50% (complete response = 1, complete response unconfirmed = 1, partial response = 1). Median progression-free survival was 3.5 months (range 1.5–10 months) and the median overall survival was 7.8 months (range 3–31 months). Grade 3–4 neutropenia and thrombocytopenia was universal, with a median of 34 (range 19–55) and 77 (range 0–275) days required for neutrophil and platelet recovery. Grade 3 non-hematologic toxicities included transaminitis, febrile neutropenia, non-neutropenic infections and orthostatic hypotension. Further accrual to the study was terminated due to prolonged Grade 3–4 myelosuppression and orthostatic hypotension in five of six patients. Clofarabine exhibits evidence of single agent activity in relapsed or refractory DLBCL. However, further study with novel administration schedules that maintain this efficacy and limit toxicity is warranted.
机译:我们评估了嘌呤核苷类似物氯法拉滨在复发或难治性弥漫性大B细胞淋巴瘤(DLBCL)和套细胞淋巴瘤(MCL)患者中的安全性和有效性。 6名DLBCL(n = 5)或MCL(n = 1)且中位年龄为68岁的患者在2小时内接受40 mg / m 2 氯法拉滨IV治疗,持续5天,每28天重复一次天,持续1-2个周期。总体回应率为50%(完全回应= 1,未确认完全回应= 1,部分回应= 1)。中位无进展生存期为3.5个月(1.5至10个月),中位总生存期为7.8个月(3至31个月)。 3-4级中性粒细胞减少和血小板减少是普遍的,中性粒细胞和血小板恢复所需的中位数为34天(19-55)和77(0-275)天。 3级非血液学毒性包括转氨酶炎,发热性中性粒细胞减少,非中性粒细胞减少感染和体位性低血压。由于六名患者中有五名患者的3-4级长期骨髓抑制和体位性低血压而终止了该研究的进一步应计。氯法拉滨在复发性或难治性DLBCL中表现出单药活性的证据。但是,有必要通过新的给药方案进行进一步研究,以保持这种功效并限制毒性。

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