Literature DB >> 27875783

PRAME overexpression predicted good outcome in pediatric B-cell acute lymphoblastic leukemia patients receiving chemotherapy.

Yan-Huan Zhang1, Ai-Dong Lu2, Lu Yang1, Ling-Di Li1, Wen-Min Chen1, Ling-Yu Long1, Le-Ping Zhang3, Ya-Zhen Qin4.   

Abstract

To investigate the prognostic value of PRAME expression in pediatric acute lymphoblastic leukemia(ALL), we measured PRAME transcript levels at diagnosis in 191 patients(146 B-ALL; 45T-ALL)receiving chemotherapy only. PRAME overexpression was defined as transcript levels higher than 0.30%, which is the upper limit of normal bone marrow and the optimal cutoff value derived from ROC curve analysis. PRAME overexpression was identified in 45.5% of patients. In B-ALL, PRAME overexpression was significantly associated with lower CIR(cumulative incidence of relapse), higher DFS (disease-freesurvival), and OS(overall survival) rates at 3 years, respectively (5.8% vs. 14.9%, P=0.014; 94.2% vs. 85.1%, P=0.014; 96.0% vs. 87.4%, P=0.039). PRAME overexpression had no impact on outcome in T-ALL patients. Among B-ALL patients with non-poor cytogenetic risk, those with PRAME overexpression showed significantly lower CIR, higher DFS and OS rates at 3 years, respectively (8.47% vs. 14.5%, P=0.009; 96.5% vs. 85.5%, P=0.009; 98.4% vs. 88.0%, P=0.023). Furthermore, PRAME overexpression was an independent good prognostic factor for relapse in all B-ALL patients and B-ALL patients with non-poor cytogenetic risk. Therefore, the prognostic significance of PRAME overexpression differed by ALL subtype; It predicted good outcome in pediatric B-ALL receiving chemotherapy.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  PRAME expression; Pediatric acute lymphoblastic leukemia; Prognosis

Mesh:

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Year:  2016        PMID: 27875783     DOI: 10.1016/j.leukres.2016.11.005

Source DB:  PubMed          Journal:  Leuk Res        ISSN: 0145-2126            Impact factor:   3.156


  4 in total

1.  [Clinical features and prognosis of childhood B-lineage acute lymphoblastic leukemia expressing the PRAME gene].

Authors:  Feng Zhang; Ai-Dong Lu; Ying-Xi Zuo; Ming-Ming Ding; Yue-Ping Jia; Le-Ping Zhang
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2022-05-15

2.  Overexpression of WT1 and PRAME predicts poor outcomes of patients with myelodysplastic syndromes with thrombocytopenia.

Authors:  Qiu-Sha Huang; Jing-Zhi Wang; Ya-Zhen Qin; Qiao-Zhu Zeng; Qian Jiang; Hao Jiang; Jin Lu; Hui-Xin Liu; Yi Liu; Jing-Bo Wang; Li Su; Hong-Yu Zhang; Zhen-Ling Li; Su-Jun Gao; Bo Huang; Yu-Ying Liu; Yan-Rong Liu; Lan-Ping Xu; Xiao-Jun Huang; Xiao-Hui Zhang
Journal:  Blood Adv       Date:  2019-11-12

Review 3.  Advances in immunotherapeutic targets for childhood cancers: A focus on glypican-2 and B7-H3.

Authors:  Nan Li; Madeline R Spetz; Dan Li; Mitchell Ho
Journal:  Pharmacol Ther       Date:  2021-05-14       Impact factor: 13.400

Review 4.  The role of the cancer testis antigen PRAME in tumorigenesis and immunotherapy in human cancer.

Authors:  Yichi Xu; Ruanmin Zou; Jing Wang; Zhi-Wei Wang; Xueqiong Zhu
Journal:  Cell Prolif       Date:  2020-02-05       Impact factor: 6.831

  4 in total

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