Wong Raymond, Shahjahan Munir, Wang Xuemei, Thall Peter F, De Lima Marcos, Khouri Issa, Gajewski James, Alamo Jorge, Couriel Daniel, Andersson Borje S, Donato Michelle, Hosing Chitra, Komanduri Krishna, Anderlini Paolo, Molldrem Jeffrey, Ueno Naoto T, Estey Elihu, Ippoliti Cindy, Champlin Richard, Giralt Sergio
Department of Blood and Marrow Transplantation, University of Texas M.D Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA.
Biol Blood Marrow Transplant. 2005 Feb;11(2):108-14. doi: 10.1016/j.bbmt.2004.10.008.
Allogeneic progenitor cell transplantation is the only curative therapy for patients with refractory acute myelogenous leukemia or myelodysplastic syndromes. To identify prognostic factors in these patients, we performed a retrospective analysis of transplantation outcomes. Patients were selected if they had undergone an allogeneic transplantation between January 1988 and January 2002 and were not in remission or first untreated relapse at the time of transplantation. A total of 135 patients were identified. The median age was 49.5 years (range, 19-75 years). At the time of transplantation, 39.3% of patients had not responded to induction therapy, 37% had not responded to first salvage therapy, and 23.7% were beyond first salvage. Forty-one patients (30%) received unrelated donor progenitor cells. Eighty patients (59%) received either a reduced-intensity or a nonmyeloablative regimen. A total of 104 (77%) of 135 patients died, with a median survival time of 4.9 months (95% confidence interval, 3.9-6.6 months). The median progression-free survival was 2.9 months (95% confidence interval, 2.5-4.2 months). A Cox regression analysis showed that Karnofsky performance status, peripheral blood blasts, and tacrolimus exposure during the first 11 days after transplantation were predictive of survival. These data support the use of allogeneic transplantation for patients with relapsed or refractory acute myelogenous leukemia/myelodysplastic syndromes and suggest that optimal immune suppression early after transplantation is essential for long-term survival even in patients with refractory myeloid leukemias.
异基因祖细胞移植是难治性急性髓系白血病或骨髓增生异常综合征患者的唯一治愈性疗法。为了确定这些患者的预后因素,我们对移植结果进行了回顾性分析。入选患者为1988年1月至2002年1月期间接受异基因移植且移植时未缓解或首次未经治疗的复发患者。共确定了135例患者。中位年龄为49.5岁(范围19 - 75岁)。移植时,39.3%的患者诱导治疗无效,37%的患者首次挽救治疗无效,23.7%的患者超过首次挽救治疗阶段。41例患者(30%)接受了无关供者的祖细胞。80例患者(59%)接受了减低强度或非清髓性方案。135例患者中有104例(77%)死亡,中位生存时间为4.9个月(95%置信区间,3.9 - 6.6个月)。中位无进展生存期为2.9个月(95%置信区间,2.5 - 4.2个月)。Cox回归分析显示,卡氏功能状态、外周血原始细胞以及移植后前11天的他克莫司暴露情况可预测生存。这些数据支持对复发或难治性急性髓系白血病/骨髓增生异常综合征患者使用异基因移植,并表明即使对于难治性髓系白血病患者,移植后早期的最佳免疫抑制对于长期生存至关重要。