Adverse prognostic impact of
KIT
exon 17 mutations despite negative flow cytometric measurable residual disease in pediatric acute myeloid leukemia with
RUNX1::RUNX1T1
Haematologica
.
2024 Sep 5.
doi: 10.3324/haematol.2024.286243.
Online ahead of print.
Authors
Shota Kato
1
,
Shin-Ichi Tsujimoto
2
,
Jun Matsubayashi
3
,
Shotaro Iwamoto
4
,
Hidefumi Hiramatsu
5
,
Yusuke Okuno
6
,
Tatsuya Kamitori
5
,
Kentaro Ohki
7
,
Takao Deguchi
8
,
Nobutaka Kiyokawa
7
,
Motohiro Kato
1
,
Junko Takita
5
,
Shiro Tanaka
9
,
Souichi Adachi
10
,
Daisuke Tomizawa
11
,
Norio Shiba
12
Affiliations
1
Department of Pediatrics, Graduate School of Medicine, the University of Tokyo, Tokyo.
2
Department of Pediatrics, Yokohama City University Graduate School of Medicine, Yokohama.
3
Center for Clinical Research and Advanced Medicine, Shiga University of Medical Science, Otsu.
4
Department of Pediatrics, Graduate School of Medicine Mie University, Tsu.
5
Department of Pediatrics, Graduate School of Medicine Kyoto University, Kyoto.
6
Department of Virology, Nagoya City University Graduate School of Medical Sciences, Nagoya.
7
Department of Pediatric Hematology and Oncology Research, National Research Institute for Child Health and Development, Tokyo.
8
Division of Cancer Immunodiagnostics, Children's Cancer Center, National Center for Child Health and Development, Tokyo.
9
Department of Clinical Biostatistics, Graduate School of Medicine, Kyoto University, Kyoto.
10
Human Health Science, Graduate School of Medicine Kyoto University, Kyoto, Japan; and.
11
Division of Leukemia and Lymphoma, Children's Cancer Center, National Center for Child Health and Development, Tokyo.
12
Department of Pediatrics, Yokohama City University Graduate School of Medicine, Yokohama.
[email protected]
.
PMID:
39234860
DOI:
10.3324/haematol.2024.286243
Abstract
Not available.