PAX5 fusion genes are frequent in poor risk childhood acute lymphoblastic leukaemia and can be targeted with BIBF1120 Journal Article


Authors: Fazio, G.; Bresolin, S.; Silvestri, D.; Quadri, M.; Saitta, C.; Vendramini, E.; Buldini, B.; Palmi, C.; Bardini, M.; Grioni, A.; Rigamonti, S.; Galbiati, M.; Mecca, S.; Savino, A. M.; Peloso, A.; Tu, J. W.; Bhatia, S.; Borkhardt, A.; Micalizzi, C.; Lo Nigro, L.; Locatelli, F.; Conter, V.; Rizzari, C.; Valsecchi, M. G.; te Kronnie, G.; Biondi, A.; Cazzaniga, G.
Article Title: PAX5 fusion genes are frequent in poor risk childhood acute lymphoblastic leukaemia and can be targeted with BIBF1120
Abstract: Background: Despite intensive risk-based treatment protocols, 15% of paediatric patients with B-Cell Precursor Acute Lymphoblastic Leukaemia (BCP-ALL) experience relapse. There is urgent need of novel strategies to target poor prognosis subgroups, like PAX5 translocated. Methods: We considered 289 childhood BCP-ALL cases consecutively enrolled in Italy in the AIEOP-BFM ALL2000/R2006 protocols and we performed extensive molecular profiling, integrating gene expression, copy number analyses and fusion genes discovery by target-capture NGS. We developed preclinical strategies to target PAX5 fusion genes. Findings: We identified 135 cases without recurrent genetic rearrangements. Among them, 59 patients (43·7%) had a Ph-like signature; the remaining cases were identified as ERG-related (26%), High-Hyperdiploid-like (17%), ETV6::RUNX1-like (8·9%), MEF2D-rearranged (2·2%) or KMT2A-like (1·5%). A poor prognosis was associated with the Ph-like signature, independently from other high-risk features. Interestingly, PAX5 was altered in 54·4% of Ph-like compared to 16·2% of non-Ph-like cases, with 7 patients carrying PAX5 fusions (PAX5t), involving either novel (ALDH18A1, IKZF1, CDH13) or known (FBRSL1, AUTS2, DACH2) partner genes. PAX5t cases have a specific driver activity signature, extending to multiple pathways including LCK hyperactivation. Among FDA-approved drugs and inhibitors, we selected Dasatinib, Bosutinib and Foretinib, in addition to Nintedanib, known to be LCK ligands. We demonstrated the efficacy of the LCK-inhibitor BIBF1120/Nintedanib, as single agent or in combination with conventional chemotherapy, both ex vivo and in patient-derived xenograft model, showing a synergistic effect with dexamethasone. Interpretation: This study provides new insights in high-risk Ph-like leukaemia and identifies a potential therapy for targeting PAX5-fusion poor risk group. Funding: Ricerca Finalizzata-Giovani Ricercatori (Italian Ministry of Health), AIRC, Transcall, Fondazione Cariparo. © 2022 The Author(s)
Keywords: childhood all; nintedanib; ph-like all; bibf1120; pax5 fusion genes
Journal Title: EBioMedicine
Volume: 83
ISSN: 2352-3964
Publisher: Elsevier Inc.  
Date Published: 2022-09-01
Start Page: 104224
Language: English
DOI: 10.1016/j.ebiom.2022.104224
PROVIDER: scopus
PMCID: PMC9403348
PUBMED: 35985167
DOI/URL:
Notes: Article -- Export Date: 1 September 2022 -- Source: Scopus
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  1. Angela Maria Savino
    6 Savino