Abstract
Cabozantinib is registered in fixed 60 mg dose. However, 46% to 62% of patients in the registration studies needed a dose reduction due to toxicity. Improved clinical efficacy has been observed in renal cell carcinoma patients (RCC) with a cabozantinib exposure greater than 750 μg/L. In our study we explored the cabozantinib exposure in patients with different tumour types. We included RCC patients from routine care and salivary gland carcinoma (SGC) patients from a phase II study with ≥1 measured Cmin at steady-state. The geometric mean (GM) Cmin at the starting dose, at 40 mg and at best tolerated dose (BTD) were compared between both tumour types. Forty-seven patients were included. All SGC patients (n = 22) started with 60 mg, while 52% of RCC patients started with 40 mg. GM Cmin at the start dose was 1456 μg/L (95% CI: 1185-1789) vs 682 μg/L (95% CI: 572-812) (P
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Krens, S. D., van Boxtel, W., Uijen, M. J. M., Jansman, F. G. A., Desar, I. M. E., Mulder, S. F., … van Erp, N. P. (2022). Exposure-toxicity relationship of cabozantinib in patients with renal cell cancer and salivary gland cancer. International Journal of Cancer, 150(2), 308–316. https://doi.org/10.1002/ijc.33797
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