Swedish Cancer Institute, Seattle, WA.
Fred Hutchinson Cancer Research Center, Seattle, WA.
JCO Oncol Pract. 2020 Jun;16(6):e464-e475. doi: 10.1200/JOP.19.00133. Epub 2020 Jan 27.
Patients with acute myeloid leukemia with high-risk cytogenetics in first complete remission (CR1) achieve better outcomes if they undergo allogeneic hematopoietic cell transplantation (HCT) compared with consolidation chemotherapy alone. However, only approximately 40% of such patients typically proceed to HCT.
We used a prospective organized approach to rapidly identify donors to improve the allogeneic HCT rate in adults with high-risk acute myeloid leukemia in CR1. Newly diagnosed patients had cytogenetics obtained at enrollment, and those with high-risk cytogenetics underwent expedited HLA typing and were encouraged to be referred for consultation with a transplantation team with the goal of conducting an allogeneic HCT in CR1.
Of 738 eligible patients (median age, 49 years; range, 18-60 years of age), 159 (22%) had high-risk cytogenetics and 107 of these patients (67%) achieved CR1. Seventy (65%) of the high-risk patients underwent transplantation in CR1 ( < .001 compared with the historical rate of 40%). Median time to HCT from CR1 was 77 days (range, 20-356 days). In landmark analysis, overall survival (OS) among patients who underwent transplantation was significantly better compared with that of patients who did not undergo transplantation (2-year OS, 48% 35%, respectively [ = .031]). Median relapse-free survival after transplantation in the high-risk cohort who underwent transplantation in CR1 (n = 70) was 11.5 months (range, 4-47 months), and median OS after transplantation was 14 months (range, 4-44 months).
Early cytogenetic testing with an organized effort to identify a suitable allogeneic HCT donor led to a CR1 transplantation rate of 65% in the high-risk group, which, in turn, led to an improvement in OS when compared with the OS of patients who did not undergo transplantation.
在首次完全缓解(CR1)的伴有高危细胞遗传学的急性髓系白血病患者中,如果接受异基因造血细胞移植(HCT),其预后优于单纯巩固化疗。然而,仅有约 40%的此类患者通常会进行 HCT。
我们采用前瞻性的有组织的方法来快速识别供者,以提高 CR1 中高危急性髓系白血病成人的异基因 HCT 率。新诊断的患者在入组时获得细胞遗传学检查结果,伴有高危细胞遗传学的患者接受加急 HLA 分型,并鼓励他们咨询移植团队,目标是在 CR1 中进行异基因 HCT。
在 738 例符合条件的患者(中位年龄,49 岁;年龄范围,18-60 岁)中,有 159 例(22%)存在高危细胞遗传学,其中 107 例(67%)达到 CR1。高危患者中有 70 例(65%)在 CR1 中进行了移植(与历史上的 40%相比,<.001)。从 CR1 到 HCT 的中位时间为 77 天(范围,20-356 天)。在里程碑分析中,接受移植的患者的总生存(OS)明显优于未接受移植的患者(2 年 OS 分别为 48%和 35%,=.031)。在 CR1 中接受移植的高危队列中,移植后无复发生存的中位时间为 11.5 个月(范围,4-47 个月),移植后 OS 的中位时间为 14 个月(范围,4-44 个月)。
通过早期细胞遗传学检测,并采用有组织的方法来识别合适的异基因 HCT 供者,使高危组的 CR1 移植率达到 65%,从而改善了与未接受移植的患者相比的 OS。