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Clinical Trials and Observations: Phase I study of obatoclax mesylate (GX15-070) a small molecule pan–Bcl-2 family antagonist in patients with advanced chronic lymphocytic leukemia

机译:临床试验和观察:甲磺酸奥马托克酯(GX15-070)一种小分子pan-Bcl-2家族拮抗剂用于晚期慢性淋巴细胞性白血病患者的I期研究

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摘要

Obatoclax mesylate is a small molecule pan–Bcl-2 antagonist with in vitro activity against chronic lymphocytic leukemia (CLL) cells. Obatoclax was administered to patients with advanced CLL at doses ranging from 3.5 to 14 mg/m2 as a 1-hour infusion and from 20 to 40 mg/m2 as a 3-hour infusion every 3 weeks. Twenty-six patients received a total of 74 cycles. Dose-limiting reactions were neurologic (somnolence, euphoria, ataxia) and associated with the infusion. The maximum tolerated dose (MTD) was 28 mg/m2 over 3 hours every 3 weeks. One (4%) of 26 patients achieved a partial response. Patients with anemia (3/11) or thrombocytopenia (4/14) experienced improvements in hemoglobin and platelet counts. Circulating lymphocyte counts were reduced in 18 of 26 patients with a median reduction of 24%. Overall, the maximum plasma concentration (Cmax) and area under the curve (AUC) values of obatoclax were dose proportional. Activation of Bax and Bak was demonstrated in peripheral blood mononuclear cells, and induction of apoptosis was related to overall obatoclax exposure, as monitored by the plasma concentration of oligonucleosomal DNA/histone complexes. Obatoclax mesylate has biologic activity and modest single-agent activity in heavily pretreated patients with advanced CLL. Further evaluation in less heavily pretreated patients and in combination with other therapeutic agents is warranted. This trial has been registered with under identifier .
机译:甲磺酸Obatoclax是一种小分子pan-Bcl-2拮抗剂,对慢性淋巴细胞性白血病(CLL)细胞具有体外活性。 Obatoclax以1小时输注剂量从3.5到14 mg / m 2 和20至40 mg / m 2 到晚期CLL患者给药每3周输注3小时。 26名患者接受了总共74个周期的治疗。剂量限制反应是神经性的(嗜睡,欣快,共济失调),并与输注有关。每3周3小时的最大耐受剂量(MTD)为28 mg / m 2 。 26名患者中有1名(4%)达到了部分缓解。贫血(3/11)或血小板减少症(4/14)的患者血红蛋白和血小板计数有所改善。 26例患者中有18例的循环淋巴细胞计数减少,中位数减少24%。总体而言,obatoclax的最大血浆浓度(Cmax)和曲线下面积(AUC)值与剂量成正比。在外周血单核细胞中证明了Bax和Bak的激活,凋亡的诱导与整体obatoclax暴露有关,如通过寡核小体DNA /组蛋白复合物的血浆浓度所监测的。甲磺酸Obatoclax在经过大量预处理的晚期CLL患者中具有生物学活性和适度的单药活性。有必要对治疗程度较轻的患者以及与其他治疗药物联合进行进一步评估。该试验已在标识符下注册。

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