Details

Autor(en) / Beteiligte

• Wang, Han
• Chan, Kathy Yuen Yee
• Cheng, Chi Keung
• Ng, Margaret H L
• Lee, Po Yi
• Cheng, Frankie Wai Tsoi
• Lam, Grace Kee See
• Chow, Tin Wai
• Ha, Shau Yin
• Chiang, Alan K S
• Leung, Wing Hang
• Leung, Anskar Y H
• Wang, Chi Chiu
• Zhang, Tao
• Zhang, Xiao-Bing
• So, Chi Chiu
• Yuen, Yuet Ping
• Sun, Qiwei
• Zhang, Chi
• Xu, Yaqun
• Cheung, John Tak Kit
• Ng, Wing Hei
• Tang, Patrick Ming-Kuen
• Kang, Wei
• To, Ka-Fai
• Lee, Wayne Yuk Wai
• Wong, Raymond S M
• Poon, Ellen Ngar Yun
• Zhao, Qi
• Huang, Junbin
• Chen, Chun
• Yuen, Patrick Man Pan
• Li, Chi-Kong
• Leung, Alex Wing Kwan
• Leung, Kam Tong

Titel

Pharmacogenomic Profiling of Pediatric Acute Myeloid Leukemia to Identify Therapeutic Vulnerabilities and Inform Functional Precision Medicine

Ist Teil von

• Blood cancer discovery, 2022-11, Vol.3 (6), p.516-535

Ort / Verlag

United States

Erscheinungsjahr

2022

Quelle

MEDLINE

Beschreibungen/Notizen

• Despite the expanding portfolio of targeted therapies for adults with acute myeloid leukemia (AML), direct implementation in children is challenging due to inherent differences in underlying genetics. Here we established the pharmacologic profile of pediatric AML by screening myeloblast sensitivity to approved and investigational agents, revealing candidates of immediate clinical relevance. Drug responses ex vivo correlated with patient characteristics, exhibited age-specific alterations, and concorded with activities in xenograft models. Integration with genomic data uncovered new gene-drug associations, suggesting actionable therapeutic vulnerabilities. Transcriptome profiling further identified gene-expression signatures associated with on- and off-target drug responses. We also demonstrated the feasibility of drug screening-guided treatment for children with high-risk AML, with two evaluable cases achieving remission. Collectively, this study offers a high-dimensional gene-drug clinical data set that could be leveraged to research the unique biology of pediatric AML and sets the stage for realizing functional precision medicine for the clinical management of the disease. We conducted integrated drug and genomic profiling of patient biopsies to build the functional genomic landscape of pediatric AML. Age-specific differences in drug response and new gene-drug interactions were identified. The feasibility of functional precision medicine-guided management of children with high-risk AML was successfully demonstrated in two evaluable clinical cases. This article is highlighted in the In This Issue feature, p. 476.