Inhibitors of KRAS(G12C) that bind the target in its inactive conformation and lock it in off-mode have shown early signs of clinical activity in patients with KRAS(G12C)-mutant lung cancer, but responses tend to be short-lived and invariably prelude the development of acquired resistance through largely unexplored mechanisms. A new study describes the emergence of RAS-MAPK heterogeneous subclonal alterations in a patient relapsed on a KRAS(G12C) inactive-state inhibitor and identifies a novel KRAS(Y96D)-resistant variant that is druggable by a next-generation compound capable of associating with KRAS(G12C) in its active configuration.

The gRASs Is Greener: Potential New Therapies in Lung Cancer with Acquired Resistance to KRASG12C Inhibitors

Pinnelli, Marika
First
;
Trusolino, Livio
Last
2021-01-01

Abstract

Inhibitors of KRAS(G12C) that bind the target in its inactive conformation and lock it in off-mode have shown early signs of clinical activity in patients with KRAS(G12C)-mutant lung cancer, but responses tend to be short-lived and invariably prelude the development of acquired resistance through largely unexplored mechanisms. A new study describes the emergence of RAS-MAPK heterogeneous subclonal alterations in a patient relapsed on a KRAS(G12C) inactive-state inhibitor and identifies a novel KRAS(Y96D)-resistant variant that is druggable by a next-generation compound capable of associating with KRAS(G12C) in its active configuration.
2021
11
8
1874-1876
1876
https://cancerdiscovery.aacrjournals.org/content/11/8/1874.long
Pinnelli, Marika; Trusolino, Livio
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1798039
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