TY - JOUR
T1 - Hyperhydration with cisplatin does not influence pemetrexed exposure
AU - de Rouw, Nikki
AU - Derijks, Hieronymus J.
AU - Hilbrands, Luuk B.
AU - Boosman, René J.
AU - Piet, Berber
AU - Koolen, Stijn L.W.
AU - Burgers, Jacobus A.
AU - Dingemans, Anne Marie C.
AU - van den Heuvel, Michel M.
AU - Hendriks, Lizza E.L.
AU - Aerts, Joachim G.J.V.
AU - Croes, Sander
AU - Mathijssen, Ron H.J.
AU - Huitema, Alwin D.R.
AU - Burger, David M.
AU - Biesma, Bonne
AU - ter Heine, Rob
N1 - Publisher Copyright:
© 2021 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.
PY - 2022/2
Y1 - 2022/2
N2 - Pemetrexed is a cytotoxic drug for first-line treatment of lung cancer. It is often combined with other anticancer drugs such as cisplatin or carboplatin. In clinical practice, hyperhydration regimens are applied to overcome cisplatin-related nephrotoxicity. As pemetrexed is almost completely eliminated from the body by the kidneys, hyperhydration can result in augmented clearance. Furthermore, administration of large quantities of fluid may increase the volume of distribution of pemetrexed. Pharmacokinetics and, thus, efficacy and toxicity may be influenced by hyperhydration. This has not yet been properly studied. We performed a population pharmacokinetic analysis to assess hyperhydration as a covariate for pemetrexed clearance and for volume of distribution A relevant change was defined as >25% increase in clearance or volume of distribution. In our extensive dataset of 133 individuals, we found that hyperhydration did not significantly or relevantly explain variability in pemetrexed clearance (unchanged, P =.196) or volume of distribution (+7% change, P =.002), despite a power of >99% to detect a relevant change. Therefore, dose adjustments of pemetrexed are not required during hyperhydration with cisplatin.
AB - Pemetrexed is a cytotoxic drug for first-line treatment of lung cancer. It is often combined with other anticancer drugs such as cisplatin or carboplatin. In clinical practice, hyperhydration regimens are applied to overcome cisplatin-related nephrotoxicity. As pemetrexed is almost completely eliminated from the body by the kidneys, hyperhydration can result in augmented clearance. Furthermore, administration of large quantities of fluid may increase the volume of distribution of pemetrexed. Pharmacokinetics and, thus, efficacy and toxicity may be influenced by hyperhydration. This has not yet been properly studied. We performed a population pharmacokinetic analysis to assess hyperhydration as a covariate for pemetrexed clearance and for volume of distribution A relevant change was defined as >25% increase in clearance or volume of distribution. In our extensive dataset of 133 individuals, we found that hyperhydration did not significantly or relevantly explain variability in pemetrexed clearance (unchanged, P =.196) or volume of distribution (+7% change, P =.002), despite a power of >99% to detect a relevant change. Therefore, dose adjustments of pemetrexed are not required during hyperhydration with cisplatin.
UR - http://www.scopus.com/inward/record.url?scp=85113388451&partnerID=8YFLogxK
U2 - 10.1111/bcp.15031
DO - 10.1111/bcp.15031
M3 - Article
C2 - 34374116
AN - SCOPUS:85113388451
SN - 0306-5251
VL - 88
SP - 871
EP - 876
JO - British Journal of Clinical Pharmacology
JF - British Journal of Clinical Pharmacology
IS - 2
ER -