细胞遗传进化对急性髓系白血病非缓解患者同种异体干细胞移植预后的影响:一项对212名受者的单研究所分析

IF 4.3 Q1 Medicine
Mitsuhiro Yuasa , Hisashi Yamamoto , Takashi Mitsuki , Kosei Kageyama , Daisuke Kaji , Yuki Taya , Aya Nishida , Kazuya Ishiwata , Shinsuke Takagi , Go Yamamoto , Yuki Asano-Mori , Atsushi Wake , Yukako Koike , Shigeyoshi Makino , Naoyuki Uchida , Shuichi Taniguchi
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引用次数: 3

摘要

遗传分析技术的最新进展有助于研究人员了解急性髓性白血病(AML)的发病机制。考虑到这一进展,AML核型仍然是提供风险适应治疗方法的最重要的预后因素之一。治疗期间核型改变时有发生,但其对预后的影响不大,特别是对同种异体干细胞移植(alloc - sct)。在这里,我们通过分析2008年至2018年期间在日本东京Toranomon医院首次接受同种异体sct的连续212例患者的结果,回顾性研究了诊断和移植前染色体变化对同种异体sct预后的影响。根据2017年欧洲白血病网风险分层对诊断和移植前的细胞遗传学异常进行分类。由于大多数患者缺乏遗传信息,本研究未考虑FLT3-ITD和NPM1等遗传异常。我们将细胞遗传进化定义为染色体从低级分类到高级分类的变化。17例(8%)患者在诊断和移植前有细胞遗传学进化,其复发率明显低于根据诊断时核型分类为中间组的患者(复发的3年置信区间[CI], 57.4%对24.9%;P & lt;. 01)。在多因素分析中,同种异体细胞移植前的细胞遗传进化对复发的CI有显著影响(风险比[HR], 3.89;CI, 1.75 ~ 8.67;P & lt;.01),且造血细胞移植特异性合并症指数得分较高(HR, 0.54;CI, 0.31 ~ 0.94;P = .03),但对总生存率和非复发死亡率没有显著影响。这些结果表明,细胞遗传学进化在同种异体细胞移植后具有显著影响,在AML治疗中应予以考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic Impact of Cytogenetic Evolution on the Outcome of Allogeneic Stem Cell Transplantation in Patients with Acute Myeloid Leukemia in Nonremission: A Single-Institute Analysis of 212 Recipients

Recent progress in genetic analysis technology has helped researchers understand the pathogenesis of acute myeloid leukemia (AML). Considering this progress, AML karyotype is still one of the most significant prognostic factors that provides risk-adapted treatment approaches. Karyotype changes during treatment have been observed at times, but their prognostic impact is sparse, especially on allogeneic stem cell transplantation (allo-SCT). Here, we retrospectively investigated the effect of chromosomal changes between diagnosis and pretransplantation on the prognosis of allo-SCT by analyzing the outcomes of 212 consecutive patients who underwent allo-SCT for the first time at Toranomon Hospital, Tokyo, Japan, between 2008 and 2018. Cytogenetic abnormalities at diagnosis and pretransplantation were categorized based on the 2017 European Leukemia Net risk stratification. Genetic abnormalities such as FLT3-ITD and NPM1 were not considered in this study due to lack of genetic information in most patients. We defined cytogenetic evolution as chromosomal changes classified from lower category to higher category. Seventeen patients (8%) had cytogenetic evolution between diagnosis and pretransplantation, and they showed a significantly worse relapse rate than those who were categorized in the intermediate group based on the karyotype at diagnosis (3-year confidence interval [CI] of relapse, 57.4% versus 24.9%; P < .01). In multivariate analysis, cytogenetic evolution before allo-SCT had a significant impact on the CI of relapse (hazard ratio [HR], 3.89; CI, 1.75 to 8.67; P < .01), as well as the high score of the hematopoietic cell transplantation-specific comorbidity index (HR, 0.54; CI, 0.31 to 0.94; P = .03), but had no significant impact on overall survival or nonrelapse mortality. These results indicate that cytogenetic evolution has a significant impact after allo-SCT and should be considered during AML treatment.

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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
1061
审稿时长
3-6 weeks
期刊介绍: Biology of Blood and Marrow Transplantation publishes original research reports, reviews, editorials, commentaries, letters to the editor, and hypotheses and is the official publication of the American Society for Transplantation and Cellular Therapy. The journal focuses on current technology and knowledge in the interdisciplinary field of hematopoetic stem cell transplantation.
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