Prostate artery chemoembolization in prostate cancer: A proof of concept study in spontaneous prostate cancer in a canine model.


Journal

Diagnostic and interventional imaging
ISSN: 2211-5684
Titre abrégé: Diagn Interv Imaging
Pays: France
ID NLM: 101568499

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 24 05 2021
revised: 08 07 2021
accepted: 20 07 2021
pubmed: 16 8 2021
medline: 15 12 2021
entrez: 15 8 2021
Statut: ppublish

Résumé

The purpose of this study was to assess the feasibility and efficacy of docetaxel-loaded bead chemoembolization in spontaneous prostate cancer in a canine model. Five pet dogs with histopathologically proven prostate cancer were referred for prostate artery chemoembolization (PACE). After PACE, all animals were followed, including pharmacokinetic study and clinical and biological evolution, until death. Pelvic contrast-enhanced computed tomography examination was performed at one and two months. Animals were subjected to pathological examination after death. Both prostate arteries were successfully chemoembolized in all dogs. A median dose of 18 mg (Q1, Q3; 11.8, 20 mg) docetaxel loaded in 3 mL of 50-100 µm super absorbent polymer beads was injected into each dog. At one month, four of the five dogs were still alive and the median prostate volume was 51% lower (prePACE median prostate volume, 18.4 mL [Q1, Q3; 12, 32.1 mL] vs. postPACE median prostate volume, 6.2 mL [Q1, Q3; 6.2, 11 mL]). At two months, three dogs died because of disease progression. The two remaining dogs showed a 70% median decrease in prostate volume. Prostate pathological examination showed 73% of necrosis. No worsening of urinary symptoms was observed. Pharmacokinetic analysis showed limited systemic passage of docetaxel. All dogs died of metastatic spread at nine months. This study suggests that PACE is feasible and safe for the treatment of spontaneous prostate cancer in a canine model and may provide a new approach to treat selected patients with prostate cancer.

Identifiants

pubmed: 34391716
pii: S2211-5684(21)00172-8
doi: 10.1016/j.diii.2021.07.003
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

709-715

Informations de copyright

Crown Copyright © 2021. Published by Elsevier Masson SAS. All rights reserved.

Auteurs

Olivier Pellerin (O)

Université de Paris, PARCC, INSERM, 75006 Paris; Department of Interventional Radiology, Hôpital Européen Georges Pompidou, Assistance Publique - Hôpitaux de Paris, 75015 Paris, France. Electronic address: olivier.pellerin@aphp.fr.

Carole Déan (C)

Department of Interventional Radiology, Hôpital Européen Georges Pompidou, Assistance Publique - Hôpitaux de Paris, 75015 Paris, France.

Philippe Reb (P)

Biosphere Medical, Parc des Nations-Paris Nord 2, 95700 Roissy-en-France.

Celine Chaix (C)

Biosphere Medical, Parc des Nations-Paris Nord 2, 95700 Roissy-en-France.

Franck Floch (F)

ONCOVET, Avenue Paul Langevin, 59650 Villeneuve d'Ascq, France.

Dominique Tierny (D)

ONCOVET, Avenue Paul Langevin, 59650 Villeneuve d'Ascq, France; OCR, Parc Eurasanté Lille Métropole, F-59120 Loos, France.

Marc Sapoval (M)

Université de Paris, PARCC, INSERM, 75006 Paris; Department of Interventional Radiology, Hôpital Européen Georges Pompidou, Assistance Publique - Hôpitaux de Paris, 75015 Paris, France.

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Classifications MeSH