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小儿B淋巴细胞白血病中孤立性髓过氧化物酶表达的临床意义

Clinical Significance of Isolated Myeloperoxidase Expression in Pediatric B-Lymphoblastic Leukemia.

作者信息

Oberley Matthew J, Li Sisi, Orgel Etan, Phei Wee Choo, Hagiya Ashley, O'Gorman Maurice R G

机构信息

Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, 4650 Sunset Blvd., Los Angeles, CA

Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles.

出版信息

Am J Clin Pathol. 2017 Apr 1;147(4):374-381. doi: 10.1093/ajcp/aqx021.

Abstract

OBJECTIVES

Diagnosis of B-cell acute lymphoblastic leukemia (B-ALL) requires immunophenotypic evidence of B-lineage and absence of specific myeloid or T-lineage markers. Rare cases of otherwise typical B-ALL express myeloperoxidase (MPO) detectable by flow cytometry with an absence of other myeloid markers, but the clinical significance of this finding is not well studied.

METHODS

A retrospective cohort analysis of flow cytometry and clinical data was performed to investigate the clinical outcome of this specific group of patients.

RESULTS

Twenty-nine cases of otherwise typical B-ALL that expressed MPO by flow cytometry (B-ALL-isoMPO) without expression of other myeloid markers were identified. The B-ALL-isoMPO group had a significantly increased incidence of relapse (univariate log rank P  = .0083; multivariate hazard ratio, 2.50; 95% confidence interval, 1.07-5.85; P  = .034) and significantly worse event-free survival by univariate analysis (log rank P  = .0066) compared with a reference group of patients with B-ALL from the same time period (n = 264).

CONCLUSIONS

To our knowledge, this is the first report to document the clinical outcomes in a group of pediatric patients with B-ALL that expresses MPO in the absence of other myeloid markers. This group had an increased rate of relapse and a worse event-free survival than the patients with B-ALL who did not express MPO.

摘要

目的

B 细胞急性淋巴细胞白血病(B-ALL)的诊断需要 B 系免疫表型证据以及缺乏特定的髓系或 T 系标志物。罕见的典型 B-ALL 病例可通过流式细胞术检测到髓过氧化物酶(MPO)表达,且无其他髓系标志物,但这一发现的临床意义尚未得到充分研究。

方法

进行了一项流式细胞术和临床数据的回顾性队列分析,以研究这一特定患者群体的临床结局。

结果

共识别出 29 例典型的 B-ALL 病例,这些病例通过流式细胞术表达 MPO(B-ALL-isoMPO),且无其他髓系标志物表达。与同期的 B-ALL 患者参考组(n = 264)相比,B-ALL-isoMPO 组的复发率显著增加(单变量对数秩检验 P = 0.0083;多变量风险比为 2.50;95%置信区间为 1.07 - 5.85;P = 0.034),且单变量分析显示无事件生存期明显更差(对数秩检验 P = 0.0066)。

结论

据我们所知,这是首份记录一组在无其他髓系标志物情况下表达 MPO 的小儿 B-ALL 患者临床结局的报告。该组患者的复发率高于未表达 MPO 的 B-ALL 患者,且无事件生存期更差。

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