Radioembolization with


Journal

Cardiovascular and interventional radiology
ISSN: 1432-086X
Titre abrégé: Cardiovasc Intervent Radiol
Pays: United States
ID NLM: 8003538

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 06 07 2019
accepted: 01 10 2019
revised: 12 09 2019
pubmed: 28 10 2019
medline: 2 10 2020
entrez: 25 10 2019
Statut: ppublish

Résumé

Peptide receptor radionuclide therapy (PRRT) and radioembolization are increasingly used in neuroendocrine neoplasms patients. However, concerns have been raised on cumulative hepatotoxicity. The aim of this sub-analysis was to investigate hepatotoxicity of yttrium-90 resin microspheres radioembolization in patients who were previously treated with PRRT. Patients treated with radioembolization after systemic radionuclide treatment were retrospectively analysed. Imaging response according to response evaluation criteria in solid tumours (RECIST) v1.1 and clinical response after 3 months were collected. Clinical, biochemical and haematological toxicities according to common terminology criteria for adverse events (CTCAE) v4.03 were also collected. Specifics on prior PRRT, subsequent radioembolization treatments, treatments after radioembolization and overall survival (OS) were collected. Forty-four patients were included, who underwent a total of 58 radioembolization procedures, of which 55% whole liver treatments, at a median of 353 days after prior PRRT. According to RECIST 1.1, an objective response rate of 16% and disease control rate of 91% were found after 3 months. Clinical response was seen in 65% (15/23) of symptomatic patients after 3 months. Within 3 months, clinical toxicities occurred in 26%. Biochemical and haematological toxicities CTCAE grade 3-4 occurred in ≤ 10%, apart from lymphocytopenia (42%). Radioembolization-related complications occurred in 5% and fatal radioembolization-induced liver disease in 2% (one patient). A median OS of 3.5 years [95% confidence interval 1.8-5.1 years] after radioembolization for the entire study population was found. Radioembolization after systemic radionuclide treatments is safe, and the occurrence of radioembolization-induced liver disease is rare. 4, case series.

Identifiants

pubmed: 31646375
doi: 10.1007/s00270-019-02350-2
pii: 10.1007/s00270-019-02350-2
pmc: PMC6965040
doi:

Substances chimiques

Receptors, Peptide 0
Yttrium Radioisotopes 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

246-253

Références

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pubmed: 21353979

Auteurs

A J A T Braat (AJAT)

Department of Radiology and Nuclear Medicine, Imaging Division, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands. a.j.a.t.braat@umcutrecht.nl.

H Ahmadzadehfar (H)

Department of Nuclear Medicine, University Hospital Bonn, Bonn, Germany.

S C Kappadath (SC)

Department of Imaging Physics, University of Texas MD Anderson Cancer Center, Houston, TX, USA.

C L Stothers (CL)

Department of Radiology and Radiologic Sciences, Vanderbilt University, Nashville, TN, USA.

A Frilling (A)

Department of Surgery and Cancer, Imperial College London, London, UK.

C M Deroose (CM)

Nuclear Medicine, University Hospital Leuven, Leuven, Belgium.

P Flamen (P)

Department of Nuclear Medicine, Jules Bordet Institute, Brussels, Belgium.

D B Brown (DB)

Department of Radiology and Radiologic Sciences, Vanderbilt University, Nashville, TN, USA.

D Y Sze (DY)

Division of Interventional Radiology, Stanford University, Palo Alto, CA, USA.

A Mahvash (A)

Department of Interventional Radiology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.

M G E H Lam (MGEH)

Department of Radiology and Nuclear Medicine, Imaging Division, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.

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Classifications MeSH