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一项评估组蛋白去乙酰化酶抑制剂 ITF2357 治疗复发或进展性多发性骨髓瘤患者的 II 期多剂量临床试验。

A phase II multiple dose clinical trial of histone deacetylase inhibitor ITF2357 in patients with relapsed or progressive multiple myeloma.

机构信息

Div. of Hematology, Ospedali Riuniti, Largo Barozzi, 1, 24128, Bergamo, Italy.

出版信息

Ann Hematol. 2010 Feb;89(2):185-90. doi: 10.1007/s00277-009-0793-8. Epub 2009 Jul 25.

DOI:10.1007/s00277-009-0793-8
PMID:19633847
Abstract

ITF2357, an orally effective member of the family of histone deacetylase inhibitors, is a potent inducer of apoptosis and death of multiple myeloma (MM) cells. We performed a phase-II, multiple-dose clinical trial in 19 patients with relapsed or progressive MM to determine the maximum tolerated dose (MTD) of ITF2357 administered twice daily for four consecutive days every week for 4 weeks (i.e., first cycle). The first six patients received 150 mg ITF2357 twice daily. Since two of them experienced a dose-limiting toxicity (DLT) during the first cycle, the subsequent patients received 100 mg ITF2357 twice daily. This was the MTD, as only one DLT occurred. Up to 12 weeks (i.e., three cycles) of treatment were scheduled. Oral dexamethasone was allowed to a maximum weekly amount of 20 mg. Median duration of treatment was 6 weeks, ranging from two (two patients) to 12 weeks (five patients). Four patients suffered from serious adverse events. Three patients experienced grade 3-4 gastro-intestinal toxicity and three had transient electrocardiographic abnormalities. Thrombocytopenia occurred in all but one patient (grade 3-4 in ten patients). At last follow-up, five patients were in stable disease, five had disease progression, and nine had died all of progressive MM. In conclusion, when given at a dose of 100 mg twice daily alone or combined with dexamethasone, ITF2357 proved tolerable but showed a modest clinical benefit in advanced MM.

摘要

ITF2357 是组蛋白去乙酰化酶抑制剂家族中一种有效的口服药物,能够诱导多发性骨髓瘤(MM)细胞凋亡和死亡。我们对 19 例复发或进展期 MM 患者进行了一项 II 期、多剂量临床研究,以确定每周连续 4 天每天两次给予 ITF2357 的最大耐受剂量(MTD),每个周期为 4 周(即第 1 周期)。前 6 例患者接受 150mg ITF2357,每日两次。由于其中 2 例在第 1 周期发生剂量限制性毒性(DLT),随后的患者接受 100mg ITF2357,每日两次。这是 MTD,因为只有 1 例发生 DLT。计划治疗 12 周(即 3 个周期)。允许口服地塞米松,每周最大剂量为 20mg。中位治疗时间为 6 周,范围从 2 周(2 例)到 12 周(5 例)。4 例患者发生严重不良事件。3 例患者出现 3-4 级胃肠道毒性,3 例患者出现短暂心电图异常。除 1 例外,所有患者均发生血小板减少症(10 例患者为 3-4 级)。最后一次随访时,5 例患者疾病稳定,5 例疾病进展,9 例死于进展性 MM。总之,当单独或与地塞米松联合使用 100mg 时,ITF2357 耐受良好,但在晚期 MM 中显示出适度的临床获益。

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