| Literature DB >> 28408464 |
Shalini C Reshmi1,2, Richard C Harvey3, Kathryn G Roberts4, Eileen Stonerock1, Amy Smith5, Heather Jenkins1, I-Ming Chen3, Marc Valentine6, Yu Liu7, Yongjin Li7, Ying Shao4, John Easton7, Debbie Payne-Turner4, Zhaohui Gu4, Thai Hoa Tran8, Jonathan V Nguyen8, Meenakshi Devidas9, Yunfeng Dai9, Nyla A Heerema2, Andrew J Carroll10, Elizabeth A Raetz11, Michael J Borowitz12, Brent L Wood13, Anne L Angiolillo14, Michael J Burke15, Wanda L Salzer16, Patrick A Zweidler-McKay17, Karen R Rabin18, William L Carroll19, Jinghui Zhang7, Mignon L Loh8, Charles G Mullighan4, Cheryl L Willman3, Julie M Gastier-Foster1,2,20, Stephen P Hunger21.
Abstract
Philadelphia chromosome-like (Ph-like) acute lymphoblastic leukemia (ALL) is a high-risk subtype characterized by genomic alterations that activate cytokine receptor and kinase signaling. We examined the frequency and spectrum of targetable genetic lesions in a retrospective cohort of 1389 consecutively diagnosed patients with childhood B-lineage ALL with high-risk clinical features and/or elevated minimal residual disease at the end of remission induction therapy. The Ph-like gene expression profile was identified in 341 of 1389 patients, 57 of whom were excluded from additional analyses because of the presence of BCR-ABL1 (n = 46) or ETV6-RUNX1 (n = 11). Among the remaining 284 patients (20.4%), overexpression and rearrangement of CRLF2 (IGH-CRLF2 or P2RY8-CRLF2) were identified in 124 (43.7%), with concomitant genomic alterations activating the JAK-STAT pathway (JAK1, JAK2, IL7R) identified in 63 patients (50.8% of those with CRLF2 rearrangement). Among the remaining patients, using reverse transcriptase polymerase chain reaction or transcriptome sequencing, we identified targetable ABL-class fusions (ABL1, ABL2, CSF1R, and PDGFRB) in 14.1%, EPOR rearrangements or JAK2 fusions in 8.8%, alterations activating other JAK-STAT signaling genes (IL7R, SH2B3, JAK1) in 6.3% or other kinases (FLT3, NTRK3, LYN) in 4.6%, and mutations involving the Ras pathway (KRAS, NRAS, NF1, PTPN11) in 6% of those with Ph-like ALL. We identified 8 new rearrangement partners for 4 kinase genes previously reported to be rearranged in Ph-like ALL. The current findings provide support for the precision-medicine testing and treatment approach for Ph-like ALL implemented in Children's Oncology Group ALL trials.Entities:
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Year: 2017 PMID: 28408464 PMCID: PMC5482101 DOI: 10.1182/blood-2016-12-758979
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113