Preconditioning intervention prior to allogeneic hematopoietic stem cell transplantation in patients with high-risk acute myeloid leukemia.

IF 2.5 4区 医学 Q2 HEMATOLOGY Experimental hematology Pub Date : 2025-02-12 DOI:10.1016/j.exphem.2025.104746
Takayoshi Tachibana, Akihiko Izumi, Shota Arai, Takaaki Takeda, Natsuki Hirose, Yotaro Tamai, Shuku Sato, Chizuko Hashimoto, Katsumichi Fujimaki, Ryuji Ishii, Hirotaka Sakai, Etsuko Yamazaki, Yasuyuki Inoue, Masatsugu Tanaka, Hideaki Nakajima
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Abstract

The outcomes of patients with high-risk acute myeloid leukemia (AML) after allogeneic hematopoietic stem cell transplantation (HCT) remain poor despite many attempts at developing therapeutic strategies. Preconditioning interventions (PCIs) have been applied to patients with high-risk AML to reduce the disease burden before starting the conditioning regimen. A single-center retrospective study was performed to evaluate the safety and efficacy of PCI in allograft patients with high-risk AML. Thirty-three patients with a median age of 57 (16-70) years were included to the entire cohort. Among various PCI regimens, venetoclax plus azacitidine was administered to 12 patients. The median drug withdrawal day was 0 days (range: 0-12) for low-intensity PCIs and 12 days (range: 8-14) for high-intensity PCIs. With no grade 3 non-hematological adverse events during PCIs, the median blast fraction in the bone marrow before and after PCIs decreased from 12.4% to 2.1% (P=0.001). Excluding three patients with early complication-related deaths, all 30 patients achieved engraftment within a median of 30 days. The overall survival, cumulative incidence of relapse, and non-relapse mortality (NRM) rates at 2 years were 67.1%, 23.9%, and 8.8%, respectively. The cumulative incidences of grade II to IV acute graft-versus-host disease (GVHD) at 100 days and chronic GVHD at 2 years were 32.4% and 23.5%, respectively. PCI may be safe and effective in promoting engraftment and reducing the risk of disease relapse without increasing the risk of non-relapse mortality. Further clinical trials are warranted to establish appropriate PCI strategies.

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异基因造血干细胞移植(HCT)后,高危急性髓性白血病(AML)患者的治疗效果仍然不佳,尽管人们多次尝试开发治疗策略。预处理干预(PCI)已被应用于高风险急性髓细胞白血病患者,以在开始调理方案前减轻疾病负担。一项单中心回顾性研究对高风险急性髓细胞白血病异体移植患者进行了PCI的安全性和有效性评估。研究共纳入33名患者,中位年龄为57(16-70)岁。在各种PCI方案中,12名患者接受了venetoclax加阿扎胞苷治疗。低强度PCI的中位停药日为0天(范围:0-12),高强度PCI的中位停药日为12天(范围:8-14)。PCI期间未发生3级非血液学不良事件,PCI前后骨髓中位鼓泡率从12.4%降至2.1%(P=0.001)。除去三名因早期并发症死亡的患者,所有30名患者均在中位30天内实现了移植。2年后的总生存率、累计复发率和非复发死亡率(NRM)分别为67.1%、23.9%和8.8%。100天时的II级至IV级急性移植物抗宿主病(GVHD)累积发生率和2年时的慢性GVHD累积发生率分别为32.4%和23.5%。PCI在促进移植和降低疾病复发风险方面可能是安全有效的,但不会增加非复发死亡风险。需要进一步开展临床试验,以确定适当的 PCI 策略。
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来源期刊
Experimental hematology
Experimental hematology 医学-血液学
CiteScore
5.30
自引率
0.00%
发文量
84
审稿时长
58 days
期刊介绍: Experimental Hematology publishes new findings, methodologies, reviews and perspectives in all areas of hematology and immune cell formation on a monthly basis that may include Special Issues on particular topics of current interest. The overall goal is to report new insights into how normal blood cells are produced, how their production is normally regulated, mechanisms that contribute to hematological diseases and new approaches to their treatment. Specific topics may include relevant developmental and aging processes, stem cell biology, analyses of intrinsic and extrinsic regulatory mechanisms, in vitro behavior of primary cells, clonal tracking, molecular and omics analyses, metabolism, epigenetics, bioengineering approaches, studies in model organisms, novel clinical observations, transplantation biology and new therapeutic avenues.
期刊最新文献
In Memoriam: Prof. Vittorio Rizzoli, The visionary who built experimental hematology in Italy Preconditioning intervention prior to allogeneic hematopoietic stem cell transplantation in patients with high-risk acute myeloid leukemia. Charting New Paths in Experimental Hematology: Revitalizing the Editorial Board and Upcoming Initiatives. CBX7 inhibitors affect H3K9 methyltransferase-regulated gene repression in leukemic cells Novel techniques to quantitatively assess age-dependent alterations in biophysical properties of HSPCs and bone marrow niche
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