Cook Gordon, Clark Richard E, Crawley Charles, Mackinnon Stephen, Russell Nigel, Thomson Kirsty, Pearce Rachel M, Towlson Keiren, Marks David I
St. James' Hospital, Leeds, and Royal Liverpool University Hospital, United Kingdom.
Biol Blood Marrow Transplant. 2006 Mar;12(3):293-300. doi: 10.1016/j.bbmt.2005.10.019.
The optimal management of patients with initially refractory acute myeloid leukemia is unknown. We analyzed the outcomes of 68 adult patients (median age, 37 years) with acute myeloid leukemia in first complete remission with initially refractory disease who were treated with matched sibling (n=44) or unrelated donor (n=22) stem cell transplantation or who received transplants from other donors (n=2). Thirty-one patients took 2 courses of chemotherapy to achieve first complete remission, a further 31 took 3 courses, and 6 patients took 4 or 5 courses. Ten patients (15%) had adverse cytogenetics. Patients were mainly conditioned with cyclophosphamide and total body irradiation (87%). Four patients (6%) did not engraft by day 28; 2 of these engrafted at 47 and 60 days. Grades II to IV and III/IV acute graft-versus-host disease (GVHD) were seen in 34% and 14% of patients, respectively. Chronic GVHD was seen in 50% of patients. The estimated actuarial disease-free and overall survivals were 34% and 37%, respectively, at 4 years. The performance status of survivors is good; 82% of patients have Karnofsky scores of 90 to 100. On multivariate analysis, overall and disease-free survival were associated with adverse cytogenetics (P=.055 and .023). Approximately one third of patients survived 4 years after allogeneic stem cell transplantation for initially refractory acute myeloid leukemia in first complete remission: relapse and treatment-related mortality were the major causes of treatment failure. Further studies are needed to determine the optimal conditioning regimens and GVHD prophylaxis.
初治难治性急性髓系白血病患者的最佳治疗方案尚不清楚。我们分析了68例成年急性髓系白血病患者(中位年龄37岁)的治疗结果,这些患者首次完全缓解但初治难治,接受了同胞匹配供者(n = 44)或非血缘供者(n = 22)的干细胞移植,或接受了来自其他供者的移植(n = 2)。31例患者接受2个疗程化疗后达到首次完全缓解,另外31例接受3个疗程,6例接受4或5个疗程。10例患者(15%)存在不良细胞遗传学特征。患者主要采用环磷酰胺和全身照射进行预处理(87%)。4例患者(6%)在第28天未植入;其中2例分别在第47天和60天植入。Ⅱ至Ⅳ级和Ⅲ/Ⅳ级急性移植物抗宿主病(GVHD)分别见于34%和14%的患者。50%的患者出现慢性GVHD。4年时估计的无病生存率和总生存率分别为34%和37%。幸存者的功能状态良好;82%的患者卡诺夫斯基评分在90至100分。多因素分析显示,总生存和无病生存与不良细胞遗传学特征相关(P = 0.055和0.023)。对于初治难治性急性髓系白血病首次完全缓解后接受异基因干细胞移植的患者,约三分之一存活4年:复发和治疗相关死亡率是治疗失败的主要原因。需要进一步研究以确定最佳预处理方案和GVHD预防措施。