Abstract

In randomized clinical trials, regorafenib (REG) has demonstrated a benefit in overall survival (OS) in mCRC patients, but limiting toxicities make treatment discontinuation frequent. Managing the high inter-patient variability of REG pharmacokinetics (PK) should help prevent toxicity and prolong the anti-tumor effect. In the prospective TEXCAN study, a sum of plasma concentrations of REG and its two main active metabolites M2 and M5 (Csum) at Day15 of Cycle 1 within 2.5 - 5.5 mg/L was associated with an improved OS (1).

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