» Articles » PMID: 33327316

Prognostic Significance of SET-NUP214 Fusion Gene in Acute Leukemia After Allogeneic Hematopoietic Stem Cell Transplantation

Overview
Specialty General Medicine
Date 2020 Dec 17
PMID 33327316
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

The SET nuclear proto-oncogene (SET)-nucleoporin (NUP) 214 fusion gene (SET-NUP214) is a rare leukemia fusion gene. Due to the limited number of samples with SET-NUP214 fusion gene in previous studies, the significance of SET-NUP214 for measurable residual disease (MRD) monitoring in patients with acute leukemia (AL) is still unclear. Our study aimed to observe the dynamic changes in SET-NUP214 expression before and after allogeneic hematopoietic stem cell transplantation (allo-HSCT), and analyzed whether SET-NUP214 could be used to evaluate MRD status. Our study included 24 AL patients who were newly diagnosed with SET-NUP214 fusion gene and they all received allo-HSCT. Their MRD was evaluated by monitoring SET-NUP214 fusion gene and leukemia-associated immunophenotype (LAIP). The median follow-up time was 501 days (56-2208 days). Of the enrolled patients, 6 (25%) patients died, including 3 (12.5%) patients died of leukemia relapse. Total 5 (20.8%) patients experienced hematological relapse at a median of 225 days (56-1057 days) post-transplantation. The SET-NUP214 median expression level at diagnosis was 405.1% (14.6%-1482.4%). SET-NUP214 gene expression generally became positive prior to flow cytometry results. In addition, the Kaplan-Meier survival curves analysis showed that those who had SET-NUP214 positive (SET-NUP214+) post-transplantation had a higher 2-year cumulative incidence of leukemia relapse (CIR) of 43.7 ± 18.8% (P < .05). However, there was no significant difference between SET-NUP214 positive and SET-NUP214 negative patients with regard to their 2-year overall survival (OS) (82.5 ± 11.3 vs 64.6 ± 17.5%, respectively, P = .271). ROC curve analysis turned out that the area under the ROC curve (AUC) was 0.916 (95% CI: 0.784-1.0; P = .005). In conclusion, SET-NUP214 fusion gene determined by real-time quantitative reverse transcriptase polymerase chain reaction (RQ-PCR) could be used to evaluate MRD status after allo-HSCT. Patients with positive SET-NUP214 expression after transplantation will have a poor prognosis.

Citing Articles

Dysregulated genes in HIGK-treated and their possible association with HNSCC.

Shanmugam S, Vijayashree Priyadharsini J, Anitha P, Smiline Girija A, Paramasivam A Mol Biol Res Commun. 2025; 14(1):59-71.

PMID: 39744516 PMC: 11624608. DOI: 10.22099/mbrc.2024.50171.1982.


SET-CAN/NUP214 fusion gene in leukemia: general features and clinical advances.

Song J, Li H, Fan S Front Oncol. 2023; 13:1269531.

PMID: 37909026 PMC: 10613893. DOI: 10.3389/fonc.2023.1269531.


Analysis of Peripheral Blood Mononuclear Cells Gene Expression Highlights the Role of Extracellular Vesicles in the Immune Response following Hematopoietic Stem Cell Transplantation in Children.

Strojny W, Kwiecinska K, Halubiec P, Kowalczyk W, Miklusiak K, Lazarczyk A Genes (Basel). 2021; 12(12).

PMID: 34946957 PMC: 8701260. DOI: 10.3390/genes12122008.


Interstitial Deletions Generating Fusion Genes.

Panagopoulos I, Heim S Cancer Genomics Proteomics. 2021; 18(3):167-196.

PMID: 33893073 PMC: 8126330. DOI: 10.21873/cgp.20251.


Determining the Appropriate Treatment for T-Cell Acute Lymphoblastic Leukemia With Fusion: Perspectives From a Case Report and Literature Review.

Lin N, Liu Z, Li Y, Yan X, Wang L Front Oncol. 2021; 11:651494.

PMID: 33869055 PMC: 8044795. DOI: 10.3389/fonc.2021.651494.

References
1.
Zhao X, Liu Y, Zhu H, Xu L, Liu D, Liu K . Monitoring MRD with flow cytometry: an effective method to predict relapse for ALL patients after allogeneic hematopoietic stem cell transplantation. Ann Hematol. 2011; 91(2):183-92. DOI: 10.1007/s00277-011-1285-1. View

2.
van der Velden V, Joosten S, Willemse M, van Wering E, Lankester A, van Dongen J . Real-time quantitative PCR for detection of minimal residual disease before allogeneic stem cell transplantation predicts outcome in children with acute lymphoblastic leukemia. Leukemia. 2001; 15(9):1485-7. DOI: 10.1038/sj.leu.2402198. View

3.
Gorello P, La Starza R, Varasano E, Chiaretti S, Elia L, Pierini V . Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults. Haematologica. 2010; 95(1):79-86. PMC: 2805748. DOI: 10.3324/haematol.2009.010413. View

4.
Salek C, Folber F, Fronkova E, Prochazka B, Marinov I, Cetkovsky P . Early MRD response as a prognostic factor in adult patients with acute lymphoblastic leukemia. Eur J Haematol. 2015; 96(3):276-84. DOI: 10.1111/ejh.12587. View

5.
Inukai T, Kiyokawa N, Campana D, Coustan-Smith E, Kikuchi A, Kobayashi M . Clinical significance of early T-cell precursor acute lymphoblastic leukaemia: results of the Tokyo Children's Cancer Study Group Study L99-15. Br J Haematol. 2011; 156(3):358-65. DOI: 10.1111/j.1365-2141.2011.08955.x. View