Selective internal radiation therapy for hepatocellular carcinoma: A 15-year multicenter Australian cohort study.


Journal

Journal of gastroenterology and hepatology
ISSN: 1440-1746
Titre abrégé: J Gastroenterol Hepatol
Pays: Australia
ID NLM: 8607909

Informations de publication

Date de publication:
Nov 2022
Historique:
revised: 27 07 2022
received: 17 05 2022
accepted: 17 08 2022
pubmed: 29 8 2022
medline: 22 11 2022
entrez: 28 8 2022
Statut: ppublish

Résumé

The exact place for selective internal radiation therapy (SIRT) in the therapeutic algorithm for hepatocellular carcinoma (HCC) is debated. There are limited data on its indications, efficacy, and safety in Australia. We performed a multicenter retrospective cohort study of patients undergoing SIRT for HCC in all Sydney hospitals between 2005 and 2019. The primary outcome was overall survival. Secondary outcomes were progression-free survival and adverse events. During the study period, 156 patients underwent SIRT across 10 institutions (mean age 67 years, 81% male). SIRT use progressively increased from 2005 (n = 2), peaking in 2017 (n = 42) before declining (2019: n = 21). Barcelona Clinic Liver Cancer stages at treatment were A (13%), B (33%), C (52%), and D (2%). Forty-four (28%) patients had tumor thrombus. After a median follow-up of 13.9 months, there were 117 deaths. Median overall survival was 15 months (95% confidence interval 11-19). Independent predictors of mortality on multivariable analysis were extent of liver involvement, Barcelona Clinic Liver Cancer stage, baseline ascites, alpha fetoprotein, and model for end-stage liver disease score. Median progression-free survival was 6.0 months (95% confidence interval 5.1-6.9 months). Following SIRT, 11% of patients were downstaged to curative therapy. SIRT-related complications occurred in 17%: radioembolization-induced liver disease (11%), pneumonitis (3%), gastrointestinal ulceration, and cholecystitis (1% each). Baseline ascites predicted for radioembolization-induced liver disease. We present the largest Australian SIRT cohort for HCC. We have identified several factors associated with a poor outcome following SIRT. Patients with early-stage disease had the best survival with some being downstaged to curative therapy.

Sections du résumé

BACKGROUND AND AIM OBJECTIVE
The exact place for selective internal radiation therapy (SIRT) in the therapeutic algorithm for hepatocellular carcinoma (HCC) is debated. There are limited data on its indications, efficacy, and safety in Australia.
METHODS METHODS
We performed a multicenter retrospective cohort study of patients undergoing SIRT for HCC in all Sydney hospitals between 2005 and 2019. The primary outcome was overall survival. Secondary outcomes were progression-free survival and adverse events.
RESULTS RESULTS
During the study period, 156 patients underwent SIRT across 10 institutions (mean age 67 years, 81% male). SIRT use progressively increased from 2005 (n = 2), peaking in 2017 (n = 42) before declining (2019: n = 21). Barcelona Clinic Liver Cancer stages at treatment were A (13%), B (33%), C (52%), and D (2%). Forty-four (28%) patients had tumor thrombus. After a median follow-up of 13.9 months, there were 117 deaths. Median overall survival was 15 months (95% confidence interval 11-19). Independent predictors of mortality on multivariable analysis were extent of liver involvement, Barcelona Clinic Liver Cancer stage, baseline ascites, alpha fetoprotein, and model for end-stage liver disease score. Median progression-free survival was 6.0 months (95% confidence interval 5.1-6.9 months). Following SIRT, 11% of patients were downstaged to curative therapy. SIRT-related complications occurred in 17%: radioembolization-induced liver disease (11%), pneumonitis (3%), gastrointestinal ulceration, and cholecystitis (1% each). Baseline ascites predicted for radioembolization-induced liver disease.
CONCLUSION CONCLUSIONS
We present the largest Australian SIRT cohort for HCC. We have identified several factors associated with a poor outcome following SIRT. Patients with early-stage disease had the best survival with some being downstaged to curative therapy.

Identifiants

pubmed: 36031345
doi: 10.1111/jgh.15986
doi:

Substances chimiques

Yttrium Radioisotopes 0
Sirtuins EC 3.5.1.-

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2173-2181

Informations de copyright

© 2022 Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.

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Auteurs

David Stephen Prince (DS)

AW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.
Department of Gastroenterology and Liver, Liverpool Hospital, Sydney, New South Wales, Australia.

Glen Schlaphoff (G)

Department of Gastroenterology and Liver, Liverpool Hospital, Sydney, New South Wales, Australia.

Scott Anthony Davison (SA)

Department of Gastroenterology and Liver, Liverpool Hospital, Sydney, New South Wales, Australia.

Ya Ruth Huo (YR)

Concord Repatriation General Hospital, Sydney, New South Wales, Australia.

Hao Xiang (H)

Concord Repatriation General Hospital, Sydney, New South Wales, Australia.

Michael Vinchill Chan (MV)

Concord Repatriation General Hospital, Sydney, New South Wales, Australia.
Sydney Adventist Hospital, Sydney, New South Wales, Australia.

Alice Unah Lee (AU)

Concord Repatriation General Hospital, Sydney, New South Wales, Australia.

Cynthuja Thailakanathan (C)

Department of Gastroenterology and Hepatology, St George Hospital, Sydney, New South Wales, Australia.

Hazem Jebeili (H)

Department of Gastroenterology and Hepatology, St George Hospital, Sydney, New South Wales, Australia.

Christopher Rogan (C)

AW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.
Sydney Adventist Hospital, Sydney, New South Wales, Australia.

Ahmed Al-Omary (A)

Gastroenterology Department, Westmead Hospital, Sydney, New South Wales, Australia.

Sidhartha Gupta (S)

Gastroenterology Department, Westmead Hospital, Sydney, New South Wales, Australia.

Ian Lockart (I)

Gastroenterology Department, St Vincent's Hospital, Sydney, New South Wales, Australia.

Neha Tiwari (N)

Department of Gastroenterology and Hepatology, Nepean Hospital, Sydney, New South Wales, Australia.

McCawley Clark-Dickson (M)

Royal North Shore Hospital, Sydney, New South Wales, Australia.

James William Hillhouse (JW)

Royal North Shore Hospital, Sydney, New South Wales, Australia.

Robyn Laube (R)

Macquarie University Hospital, Sydney, New South Wales, Australia.

Jeff Chang (J)

Department of Gastroenterology and Hepatology, Nepean Hospital, Sydney, New South Wales, Australia.
Macquarie University Hospital, Sydney, New South Wales, Australia.

Vi Nguyen (V)

Royal North Shore Hospital, Sydney, New South Wales, Australia.

Mark Danta (M)

Gastroenterology Department, St Vincent's Hospital, Sydney, New South Wales, Australia.

Robert Cheng (R)

Gastroenterology Department, Westmead Hospital, Sydney, New South Wales, Australia.

Simone Irene Strasser (SI)

AW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.

Amany Zekry (A)

Department of Gastroenterology and Hepatology, St George Hospital, Sydney, New South Wales, Australia.

Miriam Tania Levy (MT)

Department of Gastroenterology and Liver, Liverpool Hospital, Sydney, New South Wales, Australia.

Christine Chan (C)

Concord Repatriation General Hospital, Sydney, New South Wales, Australia.

Ken Liu (K)

AW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.

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