| Literature DB >> 29434963 |
Haodong Cai1, Li Yang1, Kefeng Shen1, Wei Zhang1, Jie Xiong1, Meilan Zhang1, Xia Mao1, Ying Wang1, Min Xiao1.
Abstract
E14a3 breakpoint cluster region (BCR)/ABL proto-oncogene 1, non-receptor tyrosine kinase (ABL) fusion transcript is rare in Philadelphia chromosome positive disease, particularly in acute lymphoblastic leukemia (ALL). Recently an e14a3 fusion transcript was detected by multiple laboratory examinations, and the patient was suffering from ALL. Except for the BCR/ABL fusion gene, in the present study the patient additionally had an IKAROS family zinc finger 1 deletion which, has been confirmed as a significant adverse prognosis factor. Following 2 rounds of chemotherapy, the patient presented cytological remission; however, the patient then relapsed 2 months later. They then received chimeric antigen receptor modified (CAR-modified) T-cell therapy and achieved complete remission. CAR-modified T-cell therapy is a powerful novel therapy which, exhibited great potential for treating refractory ALL, regardless of the existence and form of the BCR/ABL fusion transcript.Entities:
Keywords: CAR-modified T-cell Therapy; Philadelphia chromosome; acute lymphoblastic leukemia; breakpoint cluster region/ABL proto-oncogene 1; e14a3 (b3a3); imatinib therapy; non-receptor tyrosine kinase
Year: 2017 PMID: 29434963 PMCID: PMC5777363 DOI: 10.3892/ol.2017.7611
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967