1区 · 医学
Article
作者: Ip, Ho W. ; Tsui, Sze P. ; So, Jason C. C. ; Lee, Harold K. K. ; Wong, Kit F. ; Kho, Bonnie ; Yip, Sze F. ; Lin, Shek Y. ; Leung, Garret M. K. ; Ng, Margaret H. L. ; Luk, Tsan H. ; Leung, Anskar Y. H. ; Lau, Chi K. ; Cheng, Kelvin C. K. ; Lau, June S. M. ; Yang, Ning ; Siu, Lisa L. P. ; Au, Chun H. ; Ng, Nelson K. L. ; Kwong, Yok L. ; Lam, Stephen S. Y. ; Zhang, Chunxiao ; Ma, Edmond S. K. ; Chan, Tsun L.
AbstractThe present study aimed to define a subtype of complex/monosomal karyotype (CK/MK) acute myeloid leukemia (AML) by its distinct clinical features, p53 signaling and responses to p53 targeting agents. Ninety‐eight young adults (range: 21‐60 years; median: 49 years) with CK/MK AML were studied. They received standard induction, consolidation and allogeneic hematopoietic stem cell transplantation from siblings or matched unrelated donors if available. Chromosomal abnormalities most commonly affected chromosome 5 (30%), 7 (22%) and 17 (21%). Next generation sequencing of a 54‐myeloid gene panel were available in 76 patients. Tumor protein 53 (TP53) mutations were most common (49%) and associated with the presence of −5/5q‐ (P < .001) and −17/17p‐ (P < .001), but not −7/7q‐ (P = .370). This “typical” CK/MK AML subtype was associated with significantly lower presenting white cell counts, higher number of karyotypic abnormalities, and inferior leukemia‐free and overall survivals, compared with CK/MK AML without the typical features. Blood or bone marrow samples from typical CK/MK AML patients showed defective p53 signaling upon induction by etoposide. In vitro drug sensitivity analysis showed that they were sensitive to APR‐246 that targeted mutant p53, but resistant to MDM2 antagonist MI‐77301. Novel therapeutic strategies targeting TP53 mutations in CK/MK AML should be developed and tested in clinical trials.