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达沙替尼联合氟达拉滨治疗难治性慢性淋巴细胞白血病患者:一项多中心 2 期研究。

Dasatinib in combination with fludarabine in patients with refractory chronic lymphocytic leukemia: a multicenter phase 2 study.

机构信息

Department of Hematology, Academic Medical Centre, Amsterdam, The Netherlands; LYMMCARE (Lymphoma and Myeloma Center Amsterdam), The Netherlands.

Department of Hematology, Academic Medical Centre, Amsterdam, The Netherlands.

出版信息

Leuk Res. 2014 Jan;38(1):34-41. doi: 10.1016/j.leukres.2013.10.004. Epub 2013 Oct 28.


DOI:10.1016/j.leukres.2013.10.004
PMID:24238639
Abstract

Resistance to chemotherapy-induced apoptosis in CLL is associated with overexpression of antiapoptotic proteins induced by signals from the microenvironment. In vitro, dasatinib effectively inhibits expression of anti-apoptotic regulators and restores fludarabine sensitivity in activated CLL. The aim of this study was to evaluate efficacy of one cycle of dasatinib monotherapy (100mg/day, days 1-28) followed by combination of dasatinib with fludarabine (40mg/m²/day, days 1-3 every 28 day) for a total of 6 cycles in fludarabine-refractory CLL. The primary endpoint was overall response rate according to the IWCLL'08 criteria. 20 patients were enrolled: 18 completed at least one cycle of treatment of which 67% finished at least 2 cycles of combination treatment. 3 of these 18 patients reached a formal PR (16.7%). Majority of patients obtained some reduction in lymph node (LN) size. Most frequent toxicity was related to myelosuppression. NF-κB RNA expression levels of circulating CLL cells decreased whereas the levels of pro-apoptotic NOXA increased during treatment. In conclusion, dasatinib/fludarabine combination has modest clinical efficacy in fludarabine-refractory patients.

摘要

在 CLL 中,化疗诱导的细胞凋亡抵抗与微环境信号诱导的抗凋亡蛋白过表达有关。在体外,达沙替尼可有效抑制抗凋亡调节剂的表达,并恢复激活的 CLL 中氟达拉滨的敏感性。本研究旨在评估达沙替尼单药治疗(100mg/天,第 1-28 天)一个周期,随后联合氟达拉滨(40mg/m²/天,每 28 天第 1-3 天)共 6 个周期在氟达拉滨难治性 CLL 中的疗效。主要终点是根据 IWCLL'08 标准的总体缓解率。共纳入 20 例患者:18 例至少完成了一个周期的治疗,其中 67%的患者完成了至少 2 个周期的联合治疗。这 18 例患者中有 3 例达到了正式的 PR(16.7%)。大多数患者的淋巴结(LN)大小有所缩小。最常见的毒性与骨髓抑制有关。在治疗过程中,循环 CLL 细胞的 NF-κB RNA 表达水平下降,而促凋亡的 NOXA 水平增加。总之,达沙替尼/氟达拉滨联合治疗在氟达拉滨难治性患者中具有适度的临床疗效。

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