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Margaret Schot

Researcher at Netherlands Cancer Institute

Publications -  26
Citations -  1779

Margaret Schot is an academic researcher from Netherlands Cancer Institute. The author has contributed to research in topics: Breast cancer & Pharmacokinetics. The author has an hindex of 15, co-authored 26 publications receiving 1616 citations.

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Increased Oral Bioavailability of Topotecan in Combination With the Breast Cancer Resistance Protein and P-Glycoprotein Inhibitor GF120918

TL;DR: Coadministration of the BCRP and P-gp inhibitor GF120918 resulted in a significant increase of the systemic exposure of oral topotecan.
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Marking axillary lymph nodes with radioactive iodine seeds for axillary staging after neoadjuvant systemic treatment in breast cancer patients: the MARI procedure.

TL;DR: This study shows that marking and selectively removing metastatic lymph nodes after neoadjuvant systemic treatment has a high identification rate and a low false negative rate and the tumor response in the marked lymph node may be used to tailor further axillary treatment after NST.
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Phase I clinical and pharmacokinetic study of PNU166945, a novel water-soluble polymer-conjugated prodrug of paclitaxel

TL;DR: The presented phase I study with PNU166945, a water-soluble polymeric drug conjugate of pac litaxel, shows an alteration in pharmacokinetic behavior when paclitaxel is administered as a polymer-bound drug, Consequently, the safety profile may differ significantly from standard pac Litaxel.
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Coadministration of Cyclosporine Strongly Enhances the Oral Bioavailability of Docetaxel

TL;DR: Coadministration of oral CsA strongly enhanced the oral bioavailability of docetaxel and form the basis for the further development of a clinically useful oral formulation of docentaxel.
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Phase I and pharmacokinetic study of SPI-77, a liposomal encapsulated dosage form of cisplatin.

TL;DR: The results of this phase I trial show that the pharmacokinetic behaviour of cisplatin is significantly altered by its encapsulation in Stealth liposomes, resulting in high cholesterol concentrations and relatively low concentrations of (free) platinum in plasma, WBC and tumour tissue, which may explain the observed differences between the toxicity profiles of SPI-77.