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细胞遗传学异常及其对异基因造血干细胞移植后急性髓系白血病预后的影响:一项单中心回顾性研究

Cytogenetic Abnormalities and Their Impact on Acute Myeloid Leukemia Outcomes Following Allogeneic Hematopoietic Stem Cell Transplantation: A Single-Center Retrospective Study.

作者信息

Rashidi Amir Abbas, Kasaeian Amir, Alimoghadam Kamran, Noori Maryam, Alemi Hediyeh, Seghatoleslami Ghazal, Salehi Oveis, Ghavamzadeh Ardeshir, Vaezi Mohammad, Mousavi Seyed Asadollah, Kamranzadeh Hossein, Babakhani Davood, Rad Soroush, Barkhordar Maryam, Shiraji Sahar Tavakoli, Yaghmaie Marjan

机构信息

Hematology, Oncology and Stem Cell Transplantation Research Center, Research Institute for Oncology, Hematology and Cell Therapy, Shariati Hospital Tehran University of Medical Sciences Tehran Iran.

Liver and Pancreatobiliary Diseases Research Center, Digestive Diseases Research Institute Tehran University of Medical Sciences Tehran Iran.

出版信息

Health Sci Rep. 2025 Jun 20;8(6):e70914. doi: 10.1002/hsr2.70914. eCollection 2025 Jun.

Abstract

BACKGROUND AND AIMS

Cytogenetic abnormalities at diagnosis are detected in over half of adult patients with acute myeloid leukemia (AML). This study aimed to evaluate the impact of these abnormalities on the outcomes of AML patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT) in an Iranian cohort.

METHODS

This retrospective study included 206 AML patients aged over 15 who underwent allogeneic HSCT at a single center. Cytogenetic abnormalities were identified from medical records, and survival outcomes, including overall survival (OS) and leukemia-free survival (LFS), were assessed across different cytogenetic risk groups. Multivariable analyses were adjusted for age, sex, donor type, time from diagnosis to transplant, and disease status at transplant.

RESULTS

The median follow-up duration was 46.75 months. 1-, 3-, and 5-year OS rates were 80.0%, 65.9%, and 58.5%, respectively, with significant differences based on cytogenetic risk. Patients with -7, 7q abnormalities, +8, complex karyotype, and monosomal karyotype exhibited shorter OS, classifying them as adverse-risk. Patients with normal karyotype, inversion (16), and t(16;16) were intermediate-risk. LFS at 1, 3, and 5 years was 74.6%, 64.5%, and 54.1%, respectively, with adverse cytogenetic profiles significantly associated with shorter LFS.

CONCLUSIONS

This study demonstrates the prognostic significance of cytogenetic profiles in Iranian AML patients post-HSCT. Results underscore the importance of cytogenetic stratification in guiding treatment decisions, suggesting that risk-adapted guidelines may benefit specific populations. Future prospective studies on survival outcomes in Iranian AML patients could refine evidence-based treatment guidelines.

摘要

背景与目的

超过半数的成年急性髓系白血病(AML)患者在诊断时可检测到细胞遗传学异常。本研究旨在评估这些异常对伊朗队列中接受异基因造血干细胞移植(HSCT)的AML患者结局的影响。

方法

这项回顾性研究纳入了206例年龄超过15岁、在单一中心接受异基因HSCT的AML患者。从病历中识别细胞遗传学异常,并评估不同细胞遗传学风险组的生存结局,包括总生存期(OS)和无白血病生存期(LFS)。多变量分析对年龄、性别、供体类型、从诊断到移植的时间以及移植时的疾病状态进行了校正。

结果

中位随访时间为46.75个月。1年、3年和5年的OS率分别为80.0%、65.9%和58.5%,基于细胞遗传学风险存在显著差异。伴有-7、7q异常、+8、复杂核型和单倍体核型的患者OS较短,将其归类为不良风险。核型正常、倒位(16)和t(16;16)的患者为中等风险。1年、3年和5年的LFS分别为74.6%、64.5%和54.1%,不良细胞遗传学特征与较短的LFS显著相关。

结论

本研究证明了细胞遗传学特征在伊朗AML患者HSCT后的预后意义。结果强调了细胞遗传学分层在指导治疗决策中的重要性,表明风险适应性指南可能使特定人群受益。未来关于伊朗AML患者生存结局的前瞻性研究可能会完善基于证据的治疗指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56cd/12180083/b2ac089c9d59/HSR2-8-e70914-g002.jpg

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