[HTML][HTML] Head to head evaluation of second generation ALK inhibitors brigatinib and alectinib as first-line treatment for ALK+ NSCLC using an in silico systems biology …

E Carcereny, A Fernández-Nistal, A López, C Montoto… - Oncotarget, 2021 - ncbi.nlm.nih.gov
E Carcereny, A Fernández-Nistal, A López, C Montoto, A Naves, C Segú-Vergés, M Coma
Oncotarget, 2021ncbi.nlm.nih.gov
Abstract Around 3–7% of patients with non-small cell lung cancer (NSCLC), which represent
85% of diagnosed lung cancers, have a rearrangement in the ALK gene that produces an
abnormal activity of the ALK protein cell signaling pathway. The developed ALK tyrosine
kinase inhibitors (TKIs), such as crizotinib, ceritinib, alectinib, brigatinib and lorlatinb present
good performance treating ALK+ NSCLC, although all patients invariably develop resistance
due to ALK secondary mutations or bypass mechanisms. In the present study, we compare …
Abstract
Around 3–7% of patients with non-small cell lung cancer (NSCLC), which represent 85% of diagnosed lung cancers, have a rearrangement in the ALK gene that produces an abnormal activity of the ALK protein cell signaling pathway. The developed ALK tyrosine kinase inhibitors (TKIs), such as crizotinib, ceritinib, alectinib, brigatinib and lorlatinb present good performance treating ALK+ NSCLC, although all patients invariably develop resistance due to ALK secondary mutations or bypass mechanisms. In the present study, we compare the potential differences between brigatinib and alectinib’s mechanisms of action as first-line treatment for ALK+ NSCLC in a systems biology-based in silico setting.
ncbi.nlm.nih.gov
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