Department of Hematology, Yinzhou Hospital Affiliated to Medical School of Ningbo University, No. 251, East Baizhang Road, Yinzhou District, Ningbo, 315040, Zhejiang, China.
Department of Hematology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Ann Hematol. 2019 Sep;98(9):2073-2080. doi: 10.1007/s00277-019-03723-w. Epub 2019 Jun 14.
Patients with primary refractory or early relapsed acute myeloid leukemia (AML) have a dismal prognosis, and the treatment options for these patients are limited. The present study retrospectively examined the efficacy and toxicities of the combination of cladribine 5 mg/m per day and intermediate-dose cytarabine 1 g/m per day for 5 days and granulocyte colony-stimulating factor (G-CSF) as a salvage treatment in 36 patients with relapsed/refractory AML. Among these, 32 patients had de novo AML, and the remaining 4 patients had secondary AML. The median age for the study cohort was 45.8 years. According to the European LeukemiaNet prognostic index, 5 patients had favorable risk, 18 had intermediate risk, and 11 had poor risk. The complete remission was achieved in 58% of the patients with tolerable toxicities. Fifteen patients underwent stem cell transplantation later. Patients who underwent allogeneic hematopoietic stem cell transplantation had a significantly improved 1-year overall survival compared with those who did not (73% vs. 29%, P < 0.001). The results suggested that, as a salvage regimen, modified cladribine, cytarabine, and G-CSF were effective and well tolerated for patients with relapsed/refractory AML, especially for patients who underwent subsequent stem cell transplantation.
对于原发性难治或早期复发的急性髓系白血病(AML)患者,预后较差,这些患者的治疗选择有限。本研究回顾性分析了在 36 例复发/难治性 AML 患者中使用氯法拉滨 5mg/m 每天和中剂量阿糖胞苷 1g/m 每天连用 5 天联合粒细胞集落刺激因子(G-CSF)作为挽救治疗的疗效和毒性。其中 32 例患者为初发 AML,其余 4 例为继发性 AML。研究队列的中位年龄为 45.8 岁。根据欧洲白血病网预后指数,5 例患者为低危,18 例为中危,11 例为高危。患者对治疗有较好的耐受性,缓解率为 58%。15 例患者随后进行了干细胞移植。与未接受同种异体造血干细胞移植的患者相比,接受异基因造血干细胞移植的患者 1 年总生存率显著提高(73% vs. 29%,P < 0.001)。结果表明,改良的氯法拉滨、阿糖胞苷和 G-CSF 作为挽救方案,对复发/难治性 AML 患者有效且耐受良好,尤其是对随后接受干细胞移植的患者。