摘要
T细胞急性淋巴细胞白血病(T-cell acute lymphoblastic leukemia,T-ALL)是具有高度侵袭性的恶性肿瘤之一。NOTCH1/FBXW7突变是其最常见的一种基因突变,而SET-CAN/WT1融合基因阳性的T-ALL较少见。本文报道1例SET-CAN/WT1融合基因阳性的难治性T-ALL患者,在给予多个疗程联合化疗治疗后均无明显疗效,结合相关文献复习发现,SET-CAN/WT1融合基因阳性的T-ALL患者较为罕见,具有难治性、起病急、进展快、预后差、生存期短等特点。
T-cell acute lymphoblastic leukemia(T-ALL)is one of the highly invasive malignant tumors.NOTCH1/FBXW7 mutation is the most common gene mutation,while T-ALL with positive SET-CAN/WT1 fusion gene is rare.This paper reports a case of refractory T-ALL with positive SET-CAN/WT1 fusion gene.After several courses of combined chemotherapy,there is no obvious curative effect and related literature review.It is concluded that T-ALL patients with positive SET-CAN/WT1 fusion gene are rare,with the characteristics of refractory,acute onset,rapid progress,poor prognosis and short survival time.
作者
张研
张茜
潘耀柱
吴涛
张晓菲
刘丽超
郑瑞瑞
魏爱玲
ZHANG Yan;ZHANG Qian;PAN Yaozhu;WU Tao;ZHANG Xiaofei;LIU Lichao;ZHENG Ruirui;WEI Ailing(Department of Hematology,Joint Support Force 940 Hospital,Lanzhou,730000,China;First School of Clinical Medicine,Gansu University of Chinese Medicine;Northwest University for Nationalities)
出处
《临床血液学杂志》
CAS
2024年第3期214-216,共3页
Journal of Clinical Hematology
基金
甘肃省自然基金(No:21JR1RA183)
甘肃省卫生健康委员会项目(No:GSWSKY2021-044)
中央高校基本科研重大需求培育项目(No:31920220110)
中国人民解放军联勤保障部队第九四〇医院院内基金(No:2021yxky042)。