Goy André, Hernandez-Ilzaliturri Francisco J, Kahl Brad, Ford Peggy, Protomastro Ewelina, Berger Mark
John Theurer Cancer Center, Hackensack University Medical Center , Hackensack, NJ , USA.
Leuk Lymphoma. 2014 Dec;55(12):2761-8. doi: 10.3109/10428194.2014.907891. Epub 2014 May 6.
Obatoclax, a BH3 mimetic inhibitor of anti-apoptotic Bcl-2 proteins, demonstrates synergy with bortezomib in preclinical models of mantle cell lymphoma (MCL). This phase I/II study assessed obatoclax plus bortezomib in patients with relapsed/refractory MCL. Twenty-three patients received obatoclax 30 or 45 mg plus bortezomib 1.0 or 1.3 mg/m(2), administered intravenously on days 1, 4, 8 and 11 of a 21-day cycle. In phase I, the combination was feasible at all doses. Obatoclax 45 mg plus bortezomib 1.3 mg/m(2) was selected for phase II study. Common adverse events were somnolence (87%), fatigue (61%) and euphoric mood (57%), all primarily grade 1/2. Grade 3/4 events included thrombocytopenia (21%), anemia (13%) and fatigue (13%). Objective responses occurred in 4/13 (31%) evaluable patients (three complete and one partial response). Six patients (46%) had stable disease lasting ≥ 8 weeks. Obatoclax plus bortezomib was feasible, but the synergy demonstrated in preclinical models was not confirmed.
obatoclax是一种抗凋亡Bcl-2蛋白的BH3模拟抑制剂,在套细胞淋巴瘤(MCL)的临床前模型中显示出与硼替佐米的协同作用。这项I/II期研究评估了obatoclax联合硼替佐米治疗复发/难治性MCL患者的疗效。23例患者接受obatoclax 30或45 mg联合硼替佐米1.0或1.3 mg/m²,在21天周期的第1、4、8和11天静脉给药。在I期,所有剂量的联合用药都是可行的。选择obatoclax 45 mg联合硼替佐米1.3 mg/m²进行II期研究。常见的不良事件为嗜睡(87%)、疲劳(61%)和欣快感(57%),均主要为1/2级。3/4级事件包括血小板减少(21%)、贫血(13%)和疲劳(13%)。13例可评估患者中有4例(31%)出现客观缓解(3例完全缓解和1例部分缓解)。6例患者(46%)疾病稳定持续≥8周。Obatoclax联合硼替佐米是可行的,但临床前模型中显示的协同作用未得到证实。