| Literature DB >> 34661152 |
Aditi Shastri1,2, Jesus Gonzalez-Lugo3, Amit Verma3,2.
Abstract
Patients treated with Fms-like tyrosine kinase 3 (FLT3) inhibitor-based acute myeloid leukemia therapies nearly always develop resistance. In this issue, Alotaibi and colleagues describe the patterns of mutations that emerge upon relapse after FLT3 inhibitor therapy after initial response, as well as in treatment-refractory disease in a single-institution study; the findings offer insights for sequential therapies targeting the dominant clone at the time of relapse. See related article by Alotaibi et al., p. 125. ©2020 American Association for Cancer Research.Entities:
Year: 2020 PMID: 34661152 PMCID: PMC8447270 DOI: 10.1158/2643-3230.BCD-20-0210
Source DB: PubMed Journal: Blood Cancer Discov ISSN: 2643-3230