The prognostic factors in acute myeloid leukaemia with double‐mutated CCAAT/enhancer‐binding protein alpha (CEBPAdm)

Summary The prognostic factors to stratify acute myeloid leukaemia (AML) with double‐mutated CCAAT/enhancer‐binding protein alpha (CEBPAdm) into different risk groups remains to be determined. In this retrospective study, we evaluated 171 consecutive patients with newly diagnosed AML with CEBPAdm by...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:British journal of haematology 2022-05, Vol.197 (4), p.442-451
Hauptverfasser: Wei, Hui, Zhou, Chunlin, Liu, Bingcheng, Lin, Dong, Li, Yan, Wei, Shuning, Gong, Benfa, Zhang, Guangji, Liu, Kaiqi, Gong, Xiaoyuan, Fang, Qiuyun, Liu, Yuntao, Qiu, Shaowei, Gu, Runxia, Song, Zhen, Chen, Jiayuan, Yang, Miao, Zhang, Junping, Jin, Jingjing, Wang, Ying, Mi, Yingchang, Wang, Jianxiang
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Summary The prognostic factors to stratify acute myeloid leukaemia (AML) with double‐mutated CCAAT/enhancer‐binding protein alpha (CEBPAdm) into different risk groups remains to be determined. In this retrospective study, we evaluated 171 consecutive patients with newly diagnosed AML with CEBPAdm by a Cox proportional hazards regression model. In univariate analyses, colony stimulating factor 3 receptor (CSF3R) and Wilms tumour 1 (WT1) mutations were associated with poor relapse‐free survival (RFS). The induction regimens including homoharringtonine (omacetaxine mepesuccinate) or intermediate‐dose cytarabine was associated with favourable RFS and overall survival (OS). The induction regimen including both homoharringtonine and intermediate‐dose cytarabine was associated with the most favourable RFS (3‐year RFS 84.7%) and OS (3‐year OS 92.8%) compared to the conventional cytarabine and daunorubicin regimen (3‐year RFS 27.7%, hazard ratio [HR] 0.126, 95% confidence interval [CI] 0.051–0.313, Wald p 
ISSN:0007-1048
1365-2141
DOI:10.1111/bjh.18113