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首页> 外文期刊>Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis >Increasing aclarubicin dosage of the conventional CAG (low-dose cytarabine and aclarubicin in combination with granulocyte colony-stimulating factor) regimen is more efficacious as a salvage therapy than CAG for relapsed/refractory acute myeloid leukemia
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Increasing aclarubicin dosage of the conventional CAG (low-dose cytarabine and aclarubicin in combination with granulocyte colony-stimulating factor) regimen is more efficacious as a salvage therapy than CAG for relapsed/refractory acute myeloid leukemia

机译:对于复发/难治性急性髓细胞性白血病,常规CAG(低剂量阿糖胞苷和阿克拉比星与粒细胞集落刺激因子联合使用)方案的阿克拉比霉素剂量增加的挽救疗法比CAG更有效

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The efficacy and safety of a modified CAG (low-dose cytarabine and aclarubicin in combination with granulocyte colony-stimulating factor) regimen with an increased aclarubicin dosage [high-dose (HD)CAG] were observed in 145 patients with relapsed/refractory (R/R) acute myeloid leukemia (AML) and compared to the results of 172 patients treated with a conventional CAG regimen. The HD-CAG regimen showed both a higher complete remission (CR) rate (60.7% vs. 46.5%, 13= 0.013) and overall response (OR) rate (74.5% vs. 63.4%, P=0.039) than CAG. For patients aged <60 years, HD-CAG manifested an efficacy advantage over the CAG regimen (62.6% vs. 47.4%, P = 0.015). The 4-year overall survival (OS) rate was 30.3% +/- 13.2% with a median survival time of 19.0 +/- 5.4 months for patients re-induced with the HD-CAG regimen, which showed no significant difference compared to the CAG regimen (with a 4-year OS rate of 18.2% +/- 5.3% and a median survival time of 16.0 +/- 3.6 months, P = 0.485). The main adverse effect was myelosuppression; platelet recovery over 50 x 10(9)/L was extended by the HD-CAG regimen (15 days vs. 10 days of the CAG regimen, P = 0.003), which was tolerable and manageable. HD-CAG can safely improve efficacy compared to the CAG regimen and thus serves as an alternative treatment for R/R AML. (C) 2015 Elsevier Ltd. All rights reserved.
机译:在145例复发/难治性(R)患者中观察到改良的CAG(低剂量阿糖胞苷和阿克拉比星联合粒细胞集落刺激因子联合治疗)和阿克拉比星剂量[高剂量(HD)CAG]治疗的有效性和安全性。 / R)急性髓细胞性白血病(AML),并与采用传统CAG方案治疗的172例患者的结果进行比较。 HD-CAG方案显示出比CAG更高的完全缓解(CR)率(60.7%vs. 46.5%,13 = 0.013)和总体缓解率(OR)(74.5%vs. 63.4%,P = 0.039)。对于<60岁的患者,HD-CAG表现出优于CAG方案的疗效优势(62.6%vs. 47.4%,P = 0.015)。 HD-CAG方案再诱导的患者的4年总生存率(OS)为30.3%+/- 13.2%,中位生存时间为19.0 +/- 5.4个月,与经C-CAG方案再诱导的患者相比,无显着差异。 CAG方案(4年OS率为18.2%+/- 5.3%,中位生存时间为16.0 +/- 3.6个月,P = 0.485)。主要的不良反应是骨髓抑制。 HD-CAG方案可延长血小板恢复至50 x 10(9)/ L以上(CAG方案为15天vs. 10天,P = 0.003),这是可以忍受的和可控的。与CAG方案相比,HD-CAG可以安全地提高疗效,因此可以作为R / R AML的替代疗法。 (C)2015 Elsevier Ltd.保留所有权利。

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