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506U78用于皮肤T细胞淋巴瘤和外周T细胞淋巴瘤的II期研究结果:CALGB 59901

Results of a phase II study of 506U78 in cutaneous T-cell lymphoma and peripheral T-cell lymphoma: CALGB 59901.

作者信息

Czuczman Myron S, Porcu Pierluigi, Johnson Jeffrey, Niedzwiecki Donna, Kelly Michael, Hsi Eric D, Cook James R, Canellos George, Cheson Bruce D

机构信息

Roswell Park Cancer Institute, Buffalo, NY 14263, USA.

出版信息

Leuk Lymphoma. 2007 Jan;48(1):97-103. doi: 10.1080/10428190600961058.

Abstract

Nelarabine (compound 506U78), a novel purine nucleoside, is a soluble pro-drug of 9-beta-D-arabinofuranosylguanine (ara-G). Nelarabine is rapidly demethoxylated in blood by adenosine deaminase to ara-G. Pre-clinical and clinical studies have demonstrated the selective cytotoxicity of ara-G to T-lineage derived cells. CALGB Protocol 59901 was a Phase II study of nelarabine in patients with systemically untreated cutaneous T-cell lymphoma (CTCL) or refractory/relapsed systemic T-cell lymphoma (STCL). The objectives were to determine response rate, remission duration and safety profile associated with nelarabine given at 1.5 g m(-2) per day on days 1, 3 and 5 as an intravenous infusion every 21 days for a minimum of two cycles and to continue up to two cycles beyond CR up to a maximum of eight cycles. Nineteen patients were enrolled in the study: 11 CTCL and eight STCL patients. Grade 3 or 4 adverse events were documented in 50% and 28%, respectively. In particular, 33% of patients experienced Grade 3 or 4 neurologic toxicities. There were two partial remissions lasting 3 months and 5.5 months, respectively. Median event-free survival was 1.2 months and median overall survival was 3 months. Due to lack of efficacy and excessive toxicity, nelarabine is not recommended as monotherapy in adult patients with CTCL and STCL at this dose schedule.

摘要

奈拉滨(化合物506U78)是一种新型嘌呤核苷,是9-β-D-阿拉伯呋喃糖基鸟嘌呤(ara-G)的可溶性前体药物。奈拉滨在血液中被腺苷脱氨酶迅速脱甲氧基化为ara-G。临床前和临床研究已证明ara-G对T系来源细胞具有选择性细胞毒性。CALGB方案59901是一项关于奈拉滨治疗未经系统治疗的皮肤T细胞淋巴瘤(CTCL)或难治性/复发性系统性T细胞淋巴瘤(STCL)患者的II期研究。其目的是确定每21天静脉输注一次,在第1、3和5天给予1.5 g m(-2)剂量的奈拉滨,至少两个周期,持续至完全缓解(CR)后最多两个周期,直至最多八个周期时的缓解率、缓解持续时间和安全性。19名患者入组该研究:11名CTCL患者和8名STCL患者。分别有50%和28%的患者记录到3级或4级不良事件。特别是,33%的患者出现3级或4级神经毒性。有两次部分缓解,持续时间分别为3个月和5.5个月。无事件生存期的中位数为1.2个月,总生存期的中位数为3个月。由于疗效不佳和毒性过大,不推荐在此剂量方案下将奈拉滨作为成人CTCL和STCL患者的单一疗法。

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