EBMT Office Paris, Hôpital Saint-Antoine, Paris, France.
Service d'Hématologie Clinique et de Thérapie Cellulaire, Hôpital Saint-Antoine, Paris, France.
Am J Hematol. 2017 Jan;92(1):18-22. doi: 10.1002/ajh.24567. Epub 2016 Nov 18.
In this study, we analyzed a thiotepa-based conditioning regimen for allogeneic stem cell transplantation in adults with acute lymphoblastic leukemia, using the EBMT database. A total of 323 patients were identified. The median age was 43 years. Disease status at transplant was first complete remission (CR1) in 48.9%, CR2 in 21.7%, CR3 in 6.2%, while 23.2% of the patients had an active disease at the time of transplant. This was performed from a HLA-matched sibling (49.8%) or a matched-unrelated donor (51.2%). The incidence of acute graft-vs.-host disease (GvHD) (grade > II) was 26.6%, while chronic GvHD occurred in 35.9% of the patients at 1 year (24.6% with extensive disease). With a median follow-up of 16.8 months, the nonrelapse mortality was 12.4 and 25.3% at 100 days and 1 year, respectively. The relapse incidence at 1 year was 33.3% with no difference for patients in CR1 (27%). The one-year leukemia-free survival (LFS) and overall survival (OS) were 57 and 66%, respectively for the entire cohort and 50 and 66%, respectively in patients in CR1. Thiotepa/busulfan ± melphalan (n = 213) in comparison to thiotepa/other (n = 110) conditioning regimen resulted in higher relapse incidence at 1 year (34.9 vs. 30.3%, P = 0.016) and lower LFS (38.8 vs. 45.9%, P = 0.0203), while nonrelapse mortality (23.8 vs. 26.3%, n.s.) and OS (59.6 vs. 51.1%, P = 0.109) did not differ. This large study suggests that a thiotepa-based conditioning for allogeneic transplantation in acute lymphoblastic leukemia is feasible and effective, with the main outcomes being comparable to those achieved with other regimens. Am. J. Hematol. 92:18-22, 2017. © 2016 Wiley Periodicals, Inc.
在这项研究中,我们分析了使用 EBMT 数据库的成人急性淋巴细胞白血病患者接受含噻替哌的预处理方案的异基因干细胞移植。共确定了 323 例患者。中位年龄为 43 岁。移植时疾病状态为首次完全缓解(CR1)48.9%,CR2 为 21.7%,CR3 为 6.2%,而 23.2%的患者在移植时处于活动疾病状态。这是由 HLA 匹配的同胞(49.8%)或匹配的无关供体(51.2%)进行的。急性移植物抗宿主病(GvHD)(> II 级)的发生率为 26.6%,而在 1 年时慢性 GvHD 发生在 35.9%的患者中(广泛疾病 24.6%)。中位随访 16.8 个月,100 天时非复发死亡率为 12.4%,1 年时为 25.3%。1 年时的复发率为 33.3%,CR1 患者无差异(27%)。整个队列的 1 年无白血病生存率(LFS)和总生存率(OS)分别为 57%和 66%,CR1 患者的 1 年 LFS 和 OS 分别为 50%和 66%。噻替哌/白消安±美法仑(n=213)与噻替哌/其他(n=110)预处理方案相比,1 年时复发率更高(34.9%比 30.3%,P=0.016),LFS 更低(38.8%比 45.9%,P=0.0203),而非复发死亡率(23.8%比 26.3%,无统计学差异)和 OS(59.6%比 51.1%,P=0.109)无差异。这项大型研究表明,含噻替哌的预处理方案用于急性淋巴细胞白血病的异基因移植是可行且有效的,主要结局与其他方案相当。美国血液学杂志 92:18-22,2017。©2016 威利期刊公司