Khoury H Jean, Cortes Jorge, Baccarani Michele, Wetzler Meir, Masszi Tamas, Digumarti Raghunadharao, Craig Adam, Benichou Annie-Claude, Akard Luke
Emory University School of Medicine , Atlanta, GA , USA.
Leuk Lymphoma. 2015 Jan;56(1):120-7. doi: 10.3109/10428194.2014.889826. Epub 2014 Apr 28.
Omacetaxine mepesuccinate promotes apoptosis by inhibiting the production of short-lived oncoproteins. The efficacy and safety of omacetaxine in patients with advanced chronic myeloid leukemia (CML) previously treated with tyrosine kinase inhibitors were assessed in two phase II trials (CML-202 and CML-203). Fifty-one patients in accelerated phase (AP-CML) and 44 in myeloid blast phase (BP-CML) received subcutaneous omacetaxine 1.25 mg/m(2) twice daily days 1-14 every 28 days until hematologic response/improvement or any cytogenetic response, then days 1-7 every 28 days until disease progression. The primary endpoint was maintenance or attainment of a major hematologic response (MHR). Cytogenetic responses were also evaluated. MHR was 37% in patients with AP-CML and 9% with BP-CML (22% and 5% in those with a history of T315I). Most grade 3/4 adverse events were related to myelosuppression, and were generally manageable. Omacetaxine demonstrates activity and an acceptable safety profile in pretreated patients with advanced CML, irrespective of mutational status.
甲磺酸奥马西他辛通过抑制短命癌蛋白的产生来促进细胞凋亡。在两项II期试验(CML - 202和CML - 203)中评估了甲磺酸奥马西他辛在先前接受酪氨酸激酶抑制剂治疗的晚期慢性髓性白血病(CML)患者中的疗效和安全性。51例加速期(AP - CML)患者和44例髓系原始细胞期(BP - CML)患者接受皮下注射甲磺酸奥马西他辛1.25 mg/m²,每日两次,第1 - 14天给药,每28天重复,直至出现血液学反应/改善或任何细胞遗传学反应,然后每28天第1 - 7天给药,直至疾病进展。主要终点是维持或达到主要血液学反应(MHR)。还评估了细胞遗传学反应。AP - CML患者的MHR为37%,BP - CML患者为9%(有T315I突变史的患者分别为22%和5%)。大多数3/4级不良事件与骨髓抑制有关,且通常可控。甲磺酸奥马西他辛在先前治疗过的晚期CML患者中显示出活性和可接受的安全性,无论其突变状态如何。