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Open-label, randomized study of individualized, pharmacokinetically (PK)-guided dosing of paclitaxel combined with carboplatin in advanced Non-Small Cell Lung Cancer (NSCLC) patie…

J von Pawel, S Kraff, JR Fischer, W Eberhardt, T Gauler, L Müller, N Reinmuth, M Reck, M Kimmich, F Mayer, HG Kopp, DM Behringer, YD Ko, M Frueh, RA Hilger, M Roessler, B Moritz, U Jaehde, M Joerger · Pneumologie · 2016 · Heft 02

Dokument
1022653
CareLit-ID
Jahr
2016
Publikation
PDF
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Metadaten
DOI
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Bibliografische Angaben

Zeitschrift
Pneumologie
Autor:innen
J von Pawel, S Kraff, JR Fischer, W Eberhardt, T Gauler, L Müller, N Reinmuth, M Reck, M Kimmich, F Mayer, HG Kopp, DM Behringer, YD Ko, M Frueh, RA Hilger, M Roessler, B Moritz, U Jaehde, M Joerger
Ausgabe
Heft 02 / 2016
Seiten
–
Erschienen: 2016-02-09 00:00:00
ISSN
0934-8387

Zusammenfassung

Background: Variability of chemotherapy exposure may cause severe toxicity or lack of efficacy. Paclitaxel (PTX) exposure (time above a plasma concentration of 0.05mM, Tc > 0.05) has been shown to predict toxicity. Whereas carboplatin dose is adapted to kidney function, PTX dosing only accounts for body-surface area. We developed a PTX dosing algorithm for avoidance of supra- or subtherapeutic PTX exposure based on Tc > 0.05 determined from a single blood sample drawn 18 – 30 hours after starting PTX infusion. This study was initiated to validate PK-guided PTX dosing in advanced NSCLC patients. Methods: 304 pati…

Schlagworte

Pneumologie