Adverse prognostic impact of KIT exon 17 mutations despite negative flow cytometric measurable residual disease in pediatric acute myeloid leukemia with RUNX1::RUNX1T1

Haematologica. 2025 Jan 1;110(1):251-256. doi: 10.3324/haematol.2024.286243.
No abstract available

Grants and funding

Funding: This study was supported by a Grant-in-Aid for Scientific Research (KAKEN, grant number JP19K08350 [to NS] and JP21K15870 and JP24K11004 [to ST]) and Exploratory Research from the Ministry of Education, Culture, Sports, Science, and Technology of Japan; the Practical Research for Innovative Cancer Control from Japan Agency for Medical Research and Development (AMED, grant number JP20ck0106634 [to NS], JP17ck0106329 [to SA], JP20ck0106604 [to SA], and JP23ck0106853 [to DT]); the Project Promoting Clinical Trials for Development from AMED (grant number JP21lk0201702 [to ST]); Kawano Memorial Public Interest Incorporated Foundation for Promotion of Pediatrics, a research grant from the Japanese Society of Hematology (to NS); and a research grant from the Takeda Science Foundation (to NS).