The association of complex genetic background with the prognosis of acute leukemia with ambiguous lineage

• Published in: Scientific reports 2021-12, Vol.11 (1), p.24290-24290, Article 24290
• Main Authors: Huang, Jin, Zhou, Jing, Xiao, Min, Mao, Xia, Zhu, Li, Liu, Songya, Li, Qinlu, Wang, Jin, Zhou, Jianfeng, Cai, Haodong, Wang, Gaoxiang
• Format: Article
• Language: English
• Subjects: 631/208; 631/67; Acute Disease; Adolescent; Adult; Blast cells; Classification systems; Clinical outcomes; Female; Gene regulation; Genomic Instability; Humanities and Social Sciences; Humans; Leukemia; Leukemia - classification; Leukemia - diagnosis; Leukemia - genetics; Leukemia - metabolism; Male; Malignancy; Medical prognosis; Middle Aged; multidisciplinary; Mutation; Neoplasm Proteins - genetics; Neoplasm Proteins - metabolism; Next-generation sequencing; Patients; Phenotypes; Point mutation; Prognosis; Retrospective Studies; Runx1 protein; Science; Science (multidisciplinary); Signal transduction; Survival analysis; Transcription
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-021-03709-7

Acute leukemia with ambiguous lineage (ALAL) is a rare and highly aggressive malignancy with limited molecular characterization and therapeutic recommendations. In this study, we retrospectively analyzed 1635 acute leukemia cases in our center from January 2012 to June 2018. The diagnose of ALAL was based on either EGIL or 2016 WHO criteria, a total of 39 patients were included. Four patients diagnosed as acute undifferentiated leukemia (AUL) by both classification systems. Among the patients underwent high-throughput sequencing, 89.5% were detected at least one mutation and the median number of gene mutation was 3 (0–8) per sample. The most frequently mutated genes were NRAS (4, 21%), CEBPA (4, 21%), JAK3 (3, 16%), RUNX1 (3, 16%). The mutations detected in mixed-phenotype acute leukemia (MPAL) enriched in genes related to genomic stability and transcriptional regulation; while AUL cases frequently mutated in genes involved in signaling pathway. The survival analysis strongly suggested that mutation burden may play important roles to predict the clinical outcomes of ALAL. In addition, the patients excluded by WHO criteria had even worse clinical outcome than those included. The association of the genetic complexity of blast cells with the clinical outcomes and rationality of the diagnostic criteria of WHO system need to be evaluated by more large-scale prospective clinical studies.