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本文引用的文献

1
Intensive chemotherapy, azacitidine, or supportive care in older acute myeloid leukemia patients: an analysis from a regional healthcare network.在老年急性髓系白血病患者中强化化疗、阿扎胞苷或支持性护理:来自区域医疗保健网络的分析。
Am J Hematol. 2014 Dec;89(12):E244-52. doi: 10.1002/ajh.23848. Epub 2014 Oct 20.
2
Acute myeloid leukemia and myelodysplastic syndromes in older adults.老年急性髓系白血病和骨髓增生异常综合征
J Clin Oncol. 2014 Aug 20;32(24):2541-52. doi: 10.1200/JCO.2014.55.1564.
3
Improved survival among older acute myeloid leukemia patients - a population-based study.老年急性髓系白血病患者生存率的提高——一项基于人群的研究。
Acta Oncol. 2014 Jul;53(7):935-8. doi: 10.3109/0284186X.2014.889851. Epub 2014 Mar 10.
4
Azacitidine in untreated acute myeloid leukemia: a report on 149 patients.未治疗的急性髓系白血病中的阿扎胞苷:149 例患者报告。
Am J Hematol. 2014 Apr;89(4):410-6. doi: 10.1002/ajh.23654. Epub 2014 Feb 6.
5
Ten-day decitabine as initial therapy for newly diagnosed patients with acute myeloid leukemia unfit for intensive chemotherapy.十天的地西他滨作为新诊断的不适合强化化疗的急性髓性白血病患者的初始治疗。
Leuk Lymphoma. 2014 Jul;55(7):1533-7. doi: 10.3109/10428194.2013.856425. Epub 2014 Feb 4.
6
Effect of NPM1 and FLT3 mutations on the outcomes of elderly patients with acute myeloid leukemia receiving standard chemotherapy.NPM1 和 FLT3 突变对接受标准化疗的老年急性髓系白血病患者结局的影响。
Clin Lymphoma Myeloma Leuk. 2013 Aug;13(4):435-40. doi: 10.1016/j.clml.2013.02.021. Epub 2013 Jun 10.
7
Azacitidine in patients with WHO-defined AML - results of 155 patients from the Austrian Azacitidine Registry of the AGMT-Study Group.奥地利 AGMT 研究组的阿扎胞苷登记处对 155 例 WHO 定义的 AML 患者进行的阿扎胞苷治疗结果。
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8
Azacitidine might be beneficial in a subgroup of older AML patients compared to intensive chemotherapy: a single centre retrospective study of 227 consecutive patients.与强化化疗相比,阿扎胞苷可能对老年 AML 患者亚组有益:一项 227 例连续患者的单中心回顾性研究。
J Hematol Oncol. 2013 Apr 16;6:29. doi: 10.1186/1756-8722-6-29.
9
DNA methyltransferases in hematologic malignancies.血液系统恶性肿瘤中的 DNA 甲基转移酶。
Semin Hematol. 2013 Jan;50(1):48-60. doi: 10.1053/j.seminhematol.2013.01.005.
10
A competing risks analysis should report results on all cause-specific hazards and cumulative incidence functions.竞争风险分析应报告所有病因特异性危害和累积发生率函数的结果。
J Clin Epidemiol. 2013 Jun;66(6):648-53. doi: 10.1016/j.jclinepi.2012.09.017. Epub 2013 Feb 14.

60岁及以上新诊断急性髓系白血病患者的表观遗传学诱导化疗与标准诱导化疗的比较。

Comparison of epigenetic versus standard induction chemotherapy for newly diagnosed acute myeloid leukemia patients ≥60 years old.

作者信息

Gupta Neha, Miller Austin, Gandhi Shipra, Ford Laurie A, Vigil Carlos E, Griffiths Elizabeth A, Thompson James E, Wetzler Meir, Wang Eunice S

机构信息

Department of Medicine, SUNY-UB School of Medicine, Buffalo, New York.

Department of Biostatistics, Roswell Park Cancer Institute, Buffalo, New York.

出版信息

Am J Hematol. 2015 Jul;90(7):639-46. doi: 10.1002/ajh.24016.

DOI:10.1002/ajh.24016
PMID:25808347
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6791130/
Abstract

Older patients with acute myeloid leukemia (AML) have poor outcomes with standard induction chemotherapy. We retrospectively reviewed our institute's experience with epigenetic (Epi) versus cytarabine- and anthracycline-based intensive chemotherapy (IC) as induction in newly diagnosed AML patients aged 60 years and older. One hundred sixty-seven patients (n = 84, IC; n = 83, Epi) were assessed; 69 patients received decitabine and 14 azacitidine. Baseline characteristics between the IC and Epi patient cohorts were not statistically different except for age, initial white blood cell count, and comorbidity index. Overall response rate (ORR, 50% vs. 28%, respectively, P < 0.01) and complete response rate (CRR, 43% vs. 20%, respectively, P < 0.01) were superior following IC vs. Epi. Although univariate analysis demonstrated longer overall survival after IC (10.7 vs. 9.1 months, P = 0.012), multivariate analysis showed no independent impact of induction treatment. Treatment-related mortality was not statistically different in the two groups. Outcomes of patients with secondary, poor cytogenetic risk, FLT-3 mutated AML, or relapsed/refractory disease after IC or Epi were not significantly different. Outcomes of patients receiving IC versus a 10-day decitabine regimen (n = 63) also were not significantly different. Our results suggest that IC and Epi therapy are clinically equivalent approaches for upfront treatment of older patients with AML and that other factors (feasibility, toxicity, cost, etc.) should drive treatment decisions. Prospective randomized trials to determine the optimal induction approach for specific patient subsets are needed.

摘要

老年急性髓系白血病(AML)患者接受标准诱导化疗的预后较差。我们回顾性分析了我院对60岁及以上新诊断AML患者采用表观遗传学(Epi)诱导治疗与基于阿糖胞苷和蒽环类药物的强化化疗(IC)的经验。评估了167例患者(n = 84,IC组;n = 83,Epi组);69例患者接受了地西他滨治疗,14例接受了阿扎胞苷治疗。除年龄、初始白细胞计数和合并症指数外,IC组和Epi组患者的基线特征无统计学差异。与Epi组相比,IC组的总缓解率(ORR,分别为50%和28%,P < 0.01)和完全缓解率(CRR,分别为43%和20%,P < 0.01)更高。虽然单因素分析显示IC组的总生存期更长(10.7个月对9.1个月,P = 0.012),但多因素分析显示诱导治疗无独立影响。两组的治疗相关死亡率无统计学差异。IC组或Epi组后出现继发性、细胞遗传学风险差、FLT-3突变AML或复发/难治性疾病患者的预后无显著差异。接受IC治疗与接受10天地西他滨方案(n = 63)患者的预后也无显著差异。我们的结果表明,IC治疗和Epi治疗是老年AML患者初始治疗的临床等效方法,其他因素(可行性、毒性、成本等)应驱动治疗决策。需要进行前瞻性随机试验以确定特定患者亚组的最佳诱导治疗方法。