Comparison of clinical outcomes between preemptive and maintenance therapy after allogeneic hematopoietic stem cell transplantation for acute myeloid leukemia.

IF 1.8 4区 医学 Q3 HEMATOLOGY
International Journal of Hematology Pub Date : 2025-10-01 Epub Date: 2025-05-23 DOI:10.1007/s12185-025-04009-w
Hiroaki Konishi, Takayoshi Tachibana, Shota Arai, Akihiko Izumi, Takaaki Takeda, Natsuki Hirose, Jun Nukui, Shuku Sato, Taisei Suzuki, Ryuji Ishii, Etsuko Yamazaki, Manabu Matsunawa, Junichi Mukae, Atsushi Takahata, Masatsugu Tanaka, Takahiro Suzuki, Hideaki Nakajima
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Abstract

This study aimed to compare the efficacy and safety of preemptive and maintenance therapies as post-transplant therapy for acute myeloid leukemia (AML). Patients with AML who underwent allogeneic stem cell transplantation and received post-transplant therapy were eligible. Preemptive therapy was initiated if elevated Wilms' tumor-1 mRNA was detected in the peripheral blood. Twenty-nine patients received either preemptive (n = 12) or maintenance therapy (n = 17). The median age was 56 years (range, 18-70). The median time from transplantation to intervention was 77 days (range, 43-203) for maintenance and 346 days (range, 104-1027) for preemptive therapy. Maintenance therapy consisted of azacitidine (AZA) monotherapy in six patients, venetoclax (VEN) + AZA in five, and VEN + cytarabine (AraC) in six. Preemptive therapy consisted of AZA monotherapy in two patients, VEN + AZA in nine, and VEN + AraC in one. One-year overall survival from intervention was 92% for maintenance and 73% for preemptive therapy (P = 0.28), and 1-year event-free survival was 83% and 66%, respectively (P = 0.29). No serious adverse events or treatment-related mortality were observed in either group. Both therapies were safe and effective in preventing disease relapse. A prospective study comparing these two groups is warranted.

急性髓系白血病同种异体造血干细胞移植后预防性治疗与维持性治疗的临床效果比较。
本研究旨在比较作为急性髓性白血病(AML)移植后治疗的预防性治疗和维持性治疗的疗效和安全性。接受同种异体干细胞移植并接受移植后治疗的AML患者符合条件。如果外周血中检测到Wilms' tumor-1 mRNA升高,则开始先发制人治疗。29例患者接受了先发制人治疗(n = 12)或维持治疗(n = 17)。中位年龄为56岁(范围18-70岁)。维持治疗从移植到干预的中位时间为77天(范围43-203),先发制人治疗为346天(范围104-1027)。维持治疗包括6例阿扎胞苷(AZA)单药治疗,5例venetoclax (VEN) + AZA, 6例VEN +阿糖胞苷(AraC)。预防性治疗包括2例AZA单药治疗,9例VEN + AZA治疗,1例VEN + AraC治疗。干预后的1年总生存率为维持治疗组92%,先发制人治疗组73% (P = 0.28), 1年无事件生存率分别为83%和66% (P = 0.29)。两组均未观察到严重不良事件或治疗相关死亡率。两种治疗方法在预防疾病复发方面均安全有效。对这两组进行前瞻性研究是有必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.90
自引率
4.80%
发文量
223
审稿时长
6 months
期刊介绍: The International Journal of Hematology, the official journal of the Japanese Society of Hematology, has a long history of publishing leading research in hematology. The journal comprises articles that contribute to progress in research not only in basic hematology but also in clinical hematology, aiming to cover all aspects of this field, namely, erythrocytes, leukocytes and hematopoiesis, hemostasis, thrombosis and vascular biology, hematological malignancies, transplantation, and cell therapy. The expanded [Progress in Hematology] section integrates such relevant fields as the cell biology of stem cells and cancer cells, and clinical research in inflammation, cancer, and thrombosis. Reports on results of clinical trials are also included, thus contributing to the aim of fostering communication among researchers in the growing field of modern hematology. The journal provides the best of up-to-date information on modern hematology, presenting readers with high-impact, original work focusing on pivotal issues.
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