Effects of Protein and Calorie Restriction on the Metabolism and Toxicity Profile of Irinotecan in Cancer Patients.


Journal

Clinical pharmacology and therapeutics
ISSN: 1532-6535
Titre abrégé: Clin Pharmacol Ther
Pays: United States
ID NLM: 0372741

Informations de publication

Date de publication:
05 2021
Historique:
received: 19 05 2020
accepted: 06 10 2020
pubmed: 30 10 2020
medline: 16 9 2021
entrez: 29 10 2020
Statut: ppublish

Résumé

Preclinical data suggests that protein and calorie restriction (PCR) might improve treatment tolerability without impairing antitumor efficacy. Therefore, we have studied the influence of PCR on irinotecan pharmacokinetics and toxicity. In this crossover trial, patients with liver metastases of solid tumors were included and randomized to treatment with irinotecan preceded by 5 days of PCR (~ 30% caloric and ~ 70% protein restriction) during the first cycle and a second cycle preceded by a normal diet or vice versa. Pharmacokinetic blood sampling and biopsies of both healthy liver and liver metastases were performed. The primary end point was the relative difference in geometric means for the active metabolite SN-38 concentration in healthy liver analyzed by a linear mixed model. No significant differences were seen in irinotecan (+ 16.8%, P = 0.22) and SN-38 (+ 9.8%, P = 0.48) concentrations between PCR and normal diet in healthy liver, as well as in liver metastases (irinotecan: -38.8%, P = 0.05 and SN-38: -13.8%, P = 0.50). PCR increased irinotecan plasma area under the curve from zero to 24 hours (AUC

Identifiants

pubmed: 33119892
doi: 10.1002/cpt.2094
doi:

Substances chimiques

Irinotecan 7673326042

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

1304-1313

Informations de copyright

© 2020 The Authors Clinical Pharmacology & Therapeutics © 2020 American Society for Clinical Pharmacology and Therapeutics.

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Auteurs

Femke M de Man (FM)

Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Ruben A G van Eerden (RAG)

Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Gerdien M van Doorn (GM)

Department of Internal Medicine, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

Esther Oomen-de Hoop (E)

Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Stijn L W Koolen (SLW)

Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Department of Hospital Pharmacy, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

Joanne F Olieman (JF)

Department of Internal Medicine, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

Peter de Bruijn (P)

Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Joris N Veraart (JN)

Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Henk K van Halteren (HK)

Department of Internal Medicine, Admiraal de Ruyter Hospital, Goes, The Netherlands.

Yorick Sandberg (Y)

Department of Internal Medicine, Maasstad Hospital, Rotterdam, The Netherlands.

Adriaan Moelker (A)

Department of Radiology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

Jan N M IJzermans (JNM)

Department of Surgery, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

Martijn P Lolkema (MP)

Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

Teun van Gelder (T)

Department of Hospital Pharmacy, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

Martijn E T Dollé (MET)

Centre for Health Protection Research, National Institute for Public Health and Environment (RIVM), Bilthoven, The Netherlands.

Ron W F de Bruin (RWF)

Department of Surgery, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

Ron H J Mathijssen (RHJ)

Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

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