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一种基于组织学的急性髓系白血病新预后指数:“AML 浦安分类”的初步结果

A New Histology-Based Prognostic Index for Acute Myeloid Leukemia: Preliminary Results for the "AML Urayasu Classification".

作者信息

Mitsumori Toru, Nitta Hideaki, Takizawa Haruko, Iizuka-Honma Hiroko, Furuya Chiho, Fujishiro Maki, Tomita Shigeki, Hashizume Akane, Sawada Tomohiro, Miyake Kazunori, Okubo Mitsuo, Sekiguchi Yasunobu, Ando Miki, Noguchi Masaaki

机构信息

Department of Hematology, Juntendo University Urayasu Hospital, 2-1-1 Tomioka, Urayasu 279-0021, Japan.

Division of Hematology, Juntendo University Juntendo Hospital, Tokyo 113-0033, Japan.

出版信息

J Clin Med. 2025 Mar 15;14(6):1989. doi: 10.3390/jcm14061989.

Abstract

This study was aimed at elucidating the mechanisms underlying the development of treatment resistance in patients with acute myeloid leukemia (AML) other than M3 myeloid leukemia in order to devise ways to overcome treatment resistance and improve the treatment outcomes in these patients. : For this study, we randomly selected 35 patients with AML who had received combined cytarabine plus idarubicin treatment for new-onset AML at our hospital. We performed immunohistochemical analysis of biopsy specimens obtained from the patients to investigate the expressions of 23 treatment-resistance-related proteins, and retrospectively analyzed the correlations between the expression profiles of the resistance proteins and the patient survival. : The following four proteins were identified as being particularly significant in relation to treatment resistance and patient prognosis: (1) p53; (2) multidrug resistance-associated protein 1 (MRP1; idarubicin extracellular efflux pump); (3) aldo-keto reductase family 1 member B10 (AKR1B10; idarubicin-inactivating enzyme); and (4) AKR1B1 (competitive inhibitor of AKR1B10). Based on our findings, we propose the following Urayasu classification for AML, which we believe would be very useful for accurately stratifying patients with AML according to the predicted prognosis: Group 1 ( = 22, 63%): p53(-)/MRP1(-) associated with AKR1B10(+)/AKR1B1(+) or AKR1B10(-)/AKR1B1(-); 5-year overall survival (OS), 82%-100%; Group 2 ( = 9, 26%): p53(-)/MRP1(-) associated with AKR1B10(+)/AKR1B1(-); 5-year OS, 68%; Group 3 ( = 4, 11%): p53(+) or MRP1(+); median survival, 12-14 months; 2-year OS, 0%. : The Urayasu classification for AML is useful for predicting the prognosis of patients with AML. Group 1 in this classification included twice as many patients as that included in the Favorable prognosis group in the AML prognostic classification proposed by the European Leukemia Net. As the Urayasu classification for AML is based on the mechanisms of resistance to chemotherapy, it is not only useful for prognostic stratification of the patients, but also provides insights for developing more effective treatments for AML.

摘要

本研究旨在阐明急性髓系白血病(AML,非M3型髓系白血病)患者产生治疗耐药性的潜在机制,以便设计出克服治疗耐药性的方法并改善这些患者的治疗效果。在本研究中,我们随机选取了35例在我院接受阿糖胞苷联合伊达比星治疗新发AML的患者。我们对从患者身上获取的活检标本进行免疫组化分析,以研究23种与治疗耐药相关蛋白的表达情况,并回顾性分析耐药蛋白表达谱与患者生存率之间的相关性。以下四种蛋白被确定在治疗耐药性和患者预后方面具有特别重要的意义:(1)p53;(2)多药耐药相关蛋白1(MRP1;伊达比星细胞外流出泵);(3)醛糖酮还原酶家族1成员B10(AKR1B10;伊达比星失活酶);(4)AKR1B1(AKR1B10的竞争性抑制剂)。基于我们的研究结果,我们提出了以下AML的浦安分类法,我们认为这对于根据预测的预后准确分层AML患者非常有用:第1组(n = 22,63%):p53(-)/MRP1(-),与AKR1B10(+)/AKR1B1(+)或AKR1B10(-)/AKR1B1(-)相关;5年总生存率(OS),82% - 100%;第2组(n = 9,26%):p53(-)/MRP1(-),与AKR1B10(+)/AKR1B1(-)相关;5年OS,68%;第3组(n = 4,11%):p53(+)或MRP1(+);中位生存期,12 - 14个月;2年OS,0%。AML的浦安分类法有助于预测AML患者的预后。该分类法中的第1组患者数量是欧洲白血病网提出的AML预后分类中预后良好组患者数量的两倍。由于AML的浦安分类法基于化疗耐药机制,它不仅有助于患者的预后分层,还为开发更有效的AML治疗方法提供了思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adb8/11943192/5624a5c1318f/jcm-14-01989-g001.jpg

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