Safety and efficacy of percutaneous arterial port Implantation for Hepatic Arterial Infusion Chemotherapy.

Colorectal cancer Hepatic Arterial Infusion Chemotherapy (HAIC) Interventional radiology Liver cancer Liver metastases

Journal

European radiology
ISSN: 1432-1084
Titre abrégé: Eur Radiol
Pays: Germany
ID NLM: 9114774

Informations de publication

Date de publication:
30 Jul 2024
Historique:
received: 20 12 2023
accepted: 04 05 2024
revised: 12 04 2024
medline: 31 7 2024
pubmed: 31 7 2024
entrez: 30 7 2024
Statut: aheadofprint

Résumé

Approximately 40% of patients with colorectal cancer will develop liver metastases. Hepatic arterial infusion chemotherapy (HAIC) represents a valuable treatment option, with curative, palliative, or adjuvant intent. The aim of our study was to describe technical considerations, safety, and oncological outcomes of patients receiving HAIC. All patients who underwent percutaneous hepatic arterial port placement in our institution between 2004 and 2021 were included in this retrospective analysis. Demographic, anatomical and technical data were collected. Tumor response was assessed using RECIST 1.1. Kaplan-Meier estimates were used for overall survival (OS) and hepatic progression-free survival (PFS). Adverse events (AEs) were graded using the Clavien-Dindo classification. A total of 360 patients (median age, 58.6 years [interquartile range (IQR): 49.5-65.4]; 208 men [57.8%]) were included. Percutaneous hepatic arterial port placement was successful in 87.9% of cases, resulting in 379 port placements (431 attempts). Overall, 394 HAIC courses were delivered, mostly oxaliplatin-based (94.7%), with a median of 6 cycles per course (IQR: 3-8). AEs (all grades) were observed in 42.0% of ports (grade IIIb-V: 1.1%). Most port dysfunctions could be resolved, resulting in a 73.1% rate of HAIC resumption, without impact on OS. Median OS was 22 months (IQR: 18-24), and median hepatic PFS was 11 months (IQR: 9.5-13). Tumor downstaging allowed surgery in 35.6% of patients, with significantly longer median OS than non-operated patients (39 months [IQR: 33-79] versus 14 months [IQR: 12-16], p < 0.001). This retrospective cohort study demonstrates the feasibility, safety, and efficacy of percutaneous hepatic arterial port placement with an impact on survival for selected patients. Percutaneous hepatic arterial port placement is feasible, safe and effective with an impact on the survival of selected patients. Hepatic arterial infusion chemotherapy provides promising tumor response and overall survival, especially in cases of resection/ablation. Total complication rate of hepatic arterial infusion chemotherapy port use is high, but serious complications are rare. Port revision is often necessary but allows the resumption of hepatic arterial infusion chemotherapy without affecting overall survival.

Identifiants

pubmed: 39080068
doi: 10.1007/s00330-024-10887-1
pii: 10.1007/s00330-024-10887-1
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s), under exclusive licence to European Society of Radiology.

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Auteurs

Louis Meyblum (L)

Département d'Anesthésie, Chirurgie et Interventionnel (DACI), Service de Radiologie Interventionnelle, Gustave Roussy, Villejuif, F-94805, France.

Matthieu Faron (M)

Département d'Anesthésie, Chirurgie et Interventionnel (DACI), Service de Radiologie Interventionnelle, Gustave Roussy, Villejuif, F-94805, France.
OncoStat (U1018), Inserm, Université Paris Saclay, Gustave Roussy, Villejuif, F-94805, France.

Frédéric Deschamps (F)

Département d'Anesthésie, Chirurgie et Interventionnel (DACI), Service de Radiologie Interventionnelle, Gustave Roussy, Villejuif, F-94805, France.

Adrian Kobe (A)

Département d'Anesthésie, Chirurgie et Interventionnel (DACI), Service de Radiologie Interventionnelle, Gustave Roussy, Villejuif, F-94805, France.

Baptiste Bonnet (B)

Département d'Anesthésie, Chirurgie et Interventionnel (DACI), Service de Radiologie Interventionnelle, Gustave Roussy, Villejuif, F-94805, France.

Alice Boileve (A)

Department of Medical Oncology, Gustave Roussy, Villejuif, F-94805, France.
Dynamique des Cellules Tumorales (U-1279), Inserm, Gustave Roussy, Villejuif, F-94805, France.

Maximilliano Gelli (M)

Département d'Anesthésie, Chirurgie et Interventionnel (DACI), Service de Radiologie Interventionnelle, Gustave Roussy, Villejuif, F-94805, France.
Dynamique des Cellules Tumorales (U-1279), Inserm, Gustave Roussy, Villejuif, F-94805, France.

Valérie Boige (V)

Department of Medical Oncology, Gustave Roussy, Villejuif, F-94805, France.

Antoine Hollebecque (A)

Department of Medical Oncology, Gustave Roussy, Villejuif, F-94805, France.
Département d'Innovation Thérapeutique et d'Essais Précoces (DITEP), Gustave Roussy, Villejuif, F-94805, France.

Jerome Durand-Labrunie (J)

Department of Radiation Oncology, Gustave Roussy, Villejuif, F-94805, France.

David Malka (D)

Dynamique des Cellules Tumorales (U-1279), Inserm, Gustave Roussy, Villejuif, F-94805, France.
Department of Medical Oncology, Institut Mutualiste Monstouris, Paris, 75014, France.
Université Paris Saclay, Saint Aubin, 91190, France.

Remy Barbé (R)

Department of Medical Imaging, Gustave Roussy, Villejuif, F-94805, France.

Michel Ducreux (M)

Department of Medical Oncology, Gustave Roussy, Villejuif, F-94805, France.
Dynamique des Cellules Tumorales (U-1279), Inserm, Gustave Roussy, Villejuif, F-94805, France.
Université Paris Saclay, Saint Aubin, 91190, France.

Thierry de Baere (T)

Département d'Anesthésie, Chirurgie et Interventionnel (DACI), Service de Radiologie Interventionnelle, Gustave Roussy, Villejuif, F-94805, France.
Université Paris Saclay, Saint Aubin, 91190, France.
BIOTHERIS, Centre d'Investigation Clinique INSERM U1428, Villejuif, F-94805, France.

Lambros Tselikas (L)

Département d'Anesthésie, Chirurgie et Interventionnel (DACI), Service de Radiologie Interventionnelle, Gustave Roussy, Villejuif, F-94805, France. Lambros.tselikas@gustaveroussy.fr.
Université Paris Saclay, Saint Aubin, 91190, France. Lambros.tselikas@gustaveroussy.fr.
BIOTHERIS, Centre d'Investigation Clinique INSERM U1428, Villejuif, F-94805, France. Lambros.tselikas@gustaveroussy.fr.

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