Kim Haesook T, Soiffer Robert J, Cutler Corey, Koreth John, Nikiforow Sarah, Shapiro Roman M, Kelkar Amar, Gooptu Mahasweta, Romee Rizwan, Wu Catherine J, Antin Joseph H, Ritz Jerome, Ho Vincent T
Department of Data Science, Dana-Farber Cancer Institute, Harvard School of Public Health.
Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School.
Haematologica. 2025 Sep 1;110(9):1998-2008. doi: 10.3324/haematol.2025.287390. Epub 2025 Apr 10.
Advances in HLA typing, conditioning regimens, graft-versus-host disease (GVHD) prophylaxis/treatment, and supportive care have led to significant improvement in survival after allogeneic hematopoietic cell transplantation (alloHCT). Despite this progress, disease relapse after transplantation remains a daunting challenge and continues to be a major driver of mortality in patients with acute myeloid leukemia (AML). To assess whether progress has been made in relapse, we investigated our institution's experience with all AML patients who underwent their first allogeneic transplants from 2010 through 2022. A total of 1,169 patients were identified. The year of transplant was divided into two groups: 2010-2016 and 2017-2022. Several shifts in baseline clinical characteristics were noted during these periods. Patients who underwent transplantation in 2017-2022 were older (P<0.0001), had higher HCT-comorbidity index scores (P<0.0001), and were more likely to be transplanted in first complete remission (P<0.0001). Over these periods, we observed significant reductions in relapse (cumulative incidence at 3 years: 36% and 48%, respectively; P<0.0001) and severe acute GVHD (cumulative incidence at 6 months: 5% and 11%, respectively; P=0.0012), which resulted in significant improvement in progression-free (3-year estimates: 53% and 41%, respectively; P<0.0001) and overall survival (3-year estimates: 62% and 47%, respectively; P<0.0001). We also observed significant improvement in post-relapse survival over time for the relapse patients (2-year estimates: 23% and 12.6%, respectively; P<0.0001). Our results show that there has been an encouraging reduction in AML relapse, GVHD and mortality after alloHCT over the past decade.
人类白细胞抗原(HLA)分型、预处理方案、移植物抗宿主病(GVHD)预防/治疗以及支持治疗方面的进展,已使异基因造血细胞移植(alloHCT)后的生存率显著提高。尽管取得了这一进展,但移植后疾病复发仍然是一个艰巨的挑战,并且仍然是急性髓系白血病(AML)患者死亡的主要原因。为了评估在复发方面是否取得了进展,我们调查了本机构2010年至2022年期间接受首次异基因移植的所有AML患者的情况。共确定了1169例患者。移植年份分为两组:2010 - 2016年和2017 - 2022年。在这些时期内,注意到基线临床特征有若干变化。2017 - 2022年接受移植的患者年龄更大(P<0.0001),HCT合并症指数评分更高(P<0.0001),并且更有可能在首次完全缓解时接受移植(P<0.0001)。在这些时期内,我们观察到复发率(3年累积发生率分别为36%和48%;P<0.0001)和严重急性GVHD(6个月累积发生率分别为5%和11%;P = 0.0012)显著降低,这导致无进展生存期(3年估计值分别为53%和41%;P<0.0001)和总生存期(3年估计值分别为62%和47%;P<0.0001)显著改善。我们还观察到复发患者的复发后生存期随时间有显著改善(2年估计值分别为23%和12.6%;P<0.0001)。我们的结果表明,在过去十年中,alloHCT后AML的复发、GVHD和死亡率有了令人鼓舞的降低。