Pazopanib pharmacokinetically guided dose optimization in three cancer patients with gastrointestinal resection.

Dose escalation Gastrointestinal resections Pazopanib Therapeutic drug monitoring

Journal

Cancer chemotherapy and pharmacology
ISSN: 1432-0843
Titre abrégé: Cancer Chemother Pharmacol
Pays: Germany
ID NLM: 7806519

Informations de publication

Date de publication:
24 Aug 2023
Historique:
received: 05 06 2023
accepted: 01 08 2023
medline: 25 8 2023
pubmed: 25 8 2023
entrez: 24 8 2023
Statut: aheadofprint

Résumé

Pazopanib is approved in advanced renal cell carcinoma (RCC) and soft-tissue sarcoma at a flat-fixed dose despite a large pharmacokinetics interindividual variability and a narrow therapeutic index. To our knowledge, pazopanib exposure in patients with gastrointestinal resections (GIR) has not been described. This report focuses on feasibility of pharmacokinetics-guided dose escalation in these patients and clinical implications for their management. A retrospective data collection was performed for three patients with GIR treated with pazopanib, including pazopanib plasma concentrations (high-performance liquid chromatography with UV detection) and treatment adherence (Girerd score). First patient (55-year-old man, RCC, gastric bypass surgery) pazopanib C Optimal pazopanib exposure cannot be achieved in patients with GIR, and thus, other therapeutic strategies should be encouraged. Pretherapeutic assessment seems crucial to evaluate factors as bariatric surgery that may impact pazopanib concentrations. Therapeutic drug monitoring could be helpful to optimize pazopanib response in these patients.

Identifiants

pubmed: 37620675
doi: 10.1007/s00280-023-04574-z
pii: 10.1007/s00280-023-04574-z
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Cléa Tardy (C)

Pharmacy Department, Cochin Hospital (AP-HP), CARPEM, Paris, France. clea.tardy@aphp.fr.

Alicja Puszkiel (A)

Biologie du Médicament-Toxicologie, Cochin Hospital (AP-HP), Paris, France.
INSERM UMR-S1144, Université Paris Cité, Paris, France.

Pascaline Boudou-Rouquette (P)

Oncology Department, Cochin Hospital (AP-HP), CARPEM, Paris, France.

Sixtine De Percin (S)

Oncology Department, Cochin Hospital (AP-HP), CARPEM, Paris, France.

Jérôme Alexandre (J)

Oncology Department, Cochin Hospital (AP-HP), CARPEM, Paris, France.
Centre de Recherche des Cordeliers, Université Paris-Sorbonne, INSERM, 75005, Paris, France.

Marion Berge (M)

Pharmacy Department, Cochin Hospital (AP-HP), CARPEM, Paris, France.

Guillaume Ulmann (G)

Service de Biochimie, Cochin Hospital (AP-HP), Paris, France.

Benoit Blanchet (B)

Biologie du Médicament-Toxicologie, Cochin Hospital (AP-HP), Paris, France.

Rui Batista (R)

Pharmacy Department, Cochin Hospital (AP-HP), CARPEM, Paris, France.

Francois Goldwasser (F)

Oncology Department, Cochin Hospital (AP-HP), CARPEM, Paris, France.

Audrey Thomas Schoemann (A)

Pharmacy Department, Cochin Hospital (AP-HP), CARPEM, Paris, France.
Université Paris Cité, UMR 8038 CNRS, CiTCom, INSERM U1268, 75006, Paris, France.

Classifications MeSH