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After four weeks of consistent dosing at the same level, steady-state concentration is approximately five times higher than after a single dose

The underlying molecular mechanism is that tumours driven by BRAF V600E exhibit high extracellular signal-regulated kinase phosphorylation, which activates the mitogen-activated protein kinase (MAPK) signalling pathway, leading to unregulated cell proliferation and a poor prognosis [72]

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