Scott B L, Sandmaier B M, Storer B, Maris M B, Sorror M L, Maloney D G, Chauncey T R, Storb R, Deeg H J
Fred Hutchinson Cancer Research Center, Seattle, WA 98109-1024, USA
Leukemia. 2006 Jan;20(1):128-35. doi: 10.1038/sj.leu.2404010.
Transplant outcome was analyzed in 150 patients with myelodysplastic syndrome (MDS) or acute myelogenous leukemia transformed from MDS (tAML) conditioned with nonmyeloablative or myeloablative regimens. A total of 38 patients received nonmyeloablative regimens of 2 Gy total body irradiation alone (n=2) or with fludarabine (n=36), 90mg/m2. A total of 112 patients received a myeloablative regimen of busulfan, 16mg/ kg (targeted to 800-900 ng/ml), and cyclophosphamide 120 mg/ kg. Nonmyeloablative patients were older (median age 62 vs 52 years, P<0.001), more frequently had progressed to tAML (53 vs 31%, P=0.06), had higher risk disease by the International Prognostic Scoring System (53 vs 30%, P=0.004), had higher transplant specific comorbidity indices (68 vs 42%, P=0.01) and more frequently had durable complete responses to induction chemotherapy (58 vs 14%). Three-year overall survival (27%/48% (P=0.56)), progression-free survival (28%/4 44%, (P=0.60)), and nonrelapse mortality (41%/34%, (P=0.94)) did not differ significantly between nonmyeloblative/myeloablative conditioning. Overall (HR=0.9, P=0.84) and progression-free survivals (HR=1, P=0.93) were similar for patients with chemotherapy-induced remissions irrespective of conditioning intensity. Graft vs leukemia effects may be more important than conditioning intensity in preventing progression in patients in chemotherapy-induced remissions at the time of transplantation. Randomized prospective studies are needed to further address the optimal choice of transplant conditioning intensity in myeloid neoplasms.
对150例接受非清髓或清髓方案预处理的骨髓增生异常综合征(MDS)或由MDS转化而来的急性髓系白血病(tAML)患者的移植结局进行了分析。共有38例患者接受了仅2 Gy全身照射(n = 2)或联合氟达拉滨(n = 36,90mg/m²)的非清髓方案。共有112例患者接受了白消安16mg/kg(目标浓度为800 - 900 ng/ml)和环磷酰胺120mg/kg的清髓方案。非清髓患者年龄更大(中位年龄62岁对52岁,P<0.001),更频繁地进展为tAML(53%对31%,P = 0.06),根据国际预后评分系统疾病风险更高(53%对30%,P = 0.004),移植特异性合并症指数更高(68%对42%,P = 0.01),并且更频繁地对诱导化疗有持久完全缓解(58%对14%)。非清髓/清髓预处理之间的3年总生存率(27%/48%,P = 0.56)、无进展生存率(28%/44%,P = 0.60)和非复发死亡率(41%/34%,P = 0.94)无显著差异。无论预处理强度如何,化疗诱导缓解的患者的总生存率(HR = 0.9,P = 0.84)和无进展生存率(HR = 1,P = 0.93)相似。在移植时化疗诱导缓解的患者中,移植物抗白血病效应在预防疾病进展方面可能比预处理强度更重要。需要进行随机前瞻性研究以进一步探讨髓系肿瘤移植预处理强度的最佳选择。