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Ras pathway mutations are prevalent in relapsed childhood acute lymphoblastic leukemia and confer sensitivity to MEK inhibition

Lookup NU author(s): Professor Julie Irving, Elizabeth Matheson, Dr Helen Blair, Marian Case, Isabella Swidenbank, Dr Frida Ponthan, Professor James Allan, Professor Christine Harrison FRCPath FMedSci, Professor Hermann Josef Vormoor

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Abstract

For most children who relapse with acute lymphoblastic leukemia (ALL), the prognosis is poor, and there is a need for novel therapies to improve outcome. We screened samples from children with B-lineage ALL entered into the ALL-REZ BFM 2002 clinical trial (www.clinicaltrials.gov, #NCT00114348) for somatic mutations activating the Ras pathway (KRAS, NRAS, FLT3, and PTPN11) and showed mutation to be highly prevalent (76 from 206). Clinically, they were associated with high-risk features including early relapse, central nervous system (CNS) involvement, and specifically for NRAS/KRAS mutations, chemoresistance. KRAS mutations were associated with a reduced overall survival. Mutation screening of the matched diagnostic samples found many to be wild type (WT); however, by using more sensitive allelic-specific assays, low-level mutated subpopulations were found in many cases, suggesting that they survived up-front therapy and subsequently emerged at relapse. Preclinical evaluation of the mitogen-activated protein kinase kinase 1/2 inhibitor selumetinib (AZD6244, ARRY-142886) showed significant differential sensitivity in Ras pathway-mutated ALL compared with WT cells both in vitro and in an orthotopic xenograft model engrafted with primary ALL; in the latter, reduced RAS-mutated CNS leukemia. Given these data, clinical evaluation of selumetinib may be warranted for Ras pathway-mutated relapsed ALL.


Publication metadata

Author(s): Irving J, Matheson E, Minto L, Blair H, Case M, Halsey C, Swidenbank I, Ponthan F, Kirschner-Schwabe R, Groeneveld-Krentz S, Hof J, Allan J, Harrison C, Vormoor J, von Stackelberg A, Eckert C

Publication type: Article

Publication status: Published

Journal: Blood

Year: 2014

Volume: 124

Issue: 23

Pages: 3420-3430

Print publication date: 27/11/2014

Acceptance date: 26/08/2014

ISSN (print): 0006-4971

ISSN (electronic): 1528-0020

Publisher: American Society of Hematology

URL: http://dx.doi.org/10.1182/blood-2014-04-531871

DOI: 10.1182/blood-2014-04-531871


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Funding

Funder referenceFunder name
German Foundation for Childhood Cancer
KINDer-LEBEN Berlin
North of England Children's Cancer Research Fund
German Jose Carreras Leukemia Foundation
11007Leukaemia and Lymphoma Research Fund
C27943/A12788Cancer Research UK
KKL454Kay Kendall Leukaemia Fund

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