Transarterial Chemoembolization With Drug-Eluting Beads Versus Stereotactic Body Radiation Therapy for Hepatocellular Carcinoma: Outcomes From a Multicenter, Randomized, Phase 2 Trial (the TRENDY Trial).


Journal

International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616

Informations de publication

Date de publication:
01 09 2023
Historique:
received: 07 06 2022
revised: 11 03 2023
accepted: 24 03 2023
medline: 15 8 2023
pubmed: 11 4 2023
entrez: 10 4 2023
Statut: ppublish

Résumé

To compare transarterial chemoembolization delivered with drug eluting beads (TACE-DEB) with stereotactioc body radiation therapy (SBRT) in patients with hepatocellular carcinoma (HCC) in a multicenter randomized trial. Patients were included if they were eligible for TACE. They could also be recruited if they required treatment prior to liver transplantation. A maximum of four TACE-DEB procedures and ablation after incomplete TACE-DEB were both allowed. SBRT was delivered in six fractions of 8-9Gy. Primary end point was time to progression (TTP). Secondary endpoints were local control (LC), overall survival (OS), response rate (RR), toxicity, and quality of life (QoL). The calculated sample size was 100 patients. Between May 2015 and April 2020, 30 patients were randomized to the study. Due to slow accrual the trial was closed prematurely. Two patients in the SBRT arm were considered ineligible leaving 16 patients in the TACE-DEB arm and 12 in the SBRT arm. Median follow-up was 28.1 months. Median TTP was 12 months for TACEDEB and 19 months for SBRT (p=0.15). Median LC was 12 months for TACE-DEB and >40 months (not reached) for SBRT (p=0.075). Median OS was 36.8 months for TACEDEB and 44.1 months for SBRT (p=0.36). A post-hoc analysis showed 100% for SBRT 1- and 2-year LC, and 54.4% and 43.6% for TACE-DEB (p=0.019). Both treatments resulted in RR>80%. Three episodes of possibly related toxicity grade ≥3 were observed after TACE-DEB. No episodes were observed after SBRT. QoL remained stable after both treatment arms. In this trial, TTP after TACE-DEB was not significantly improved by SBRT, while SBRT showed higher local antitumoral activity than TACE-DEB, without detrimental effects on OS, toxicity and QoL. To overcome poor accrual in randomized trials that include SBRT, and to generate evidence for including SBRT in treatment guidelines, international cooperation is needed.

Identifiants

pubmed: 37037359
pii: S0360-3016(23)00308-5
doi: 10.1016/j.ijrobp.2023.03.064
pii:
doi:

Types de publication

Randomized Controlled Trial Multicenter Study Clinical Trial, Phase II Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

45-52

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.

Auteurs

Alejandra Méndez Romero (A)

Department of Radiotherapy, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands. Electronic address: a.mendezromero@erasmusmc.nl.

Bronno van der Holt (B)

Department of Radiotherapy, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.

Francois E J A Willemssen (FEJA)

Departments of Radiology and Nuclear Medicine, Erasmus MC University Medical Center, Rotterdam, The Netherlands.

Rob A de Man (RA)

Departments of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands.

Ben J M Heijmen (BJM)

Department of Radiotherapy, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.

Steven Habraken (S)

Department of Radiotherapy, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.

Henrike Westerveld (H)

Departments of Radiation Oncology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.

Otto M van Delden (OM)

Departments of Radiology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.

Heinz-Josef Klümpen (HJ)

Departments of Medical Oncology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.

Eric T T L Tjwa (ETTL)

Departments of Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen, The Netherlands.

Pètra M Braam (PM)

Departments of Radiation Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.

Sjoerd F M Jenniskens (SFM)

Departments of Radiology, Radboud University Medical Center, Nijmegen, The Netherlands.

Thomas Vanwolleghem (T)

Department of Gastroenterology and Hepatology, University Hospital Antwerp, Edegem, Belgium.

Reinhilde Weytjens (R)

Department of Radiation Oncology, Iridium Kankernetwerk, Antwerp, Belgium; Department of Molecular Imaging, Pathology, Radiotherapy, and Oncology (MIPRO), Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.

Olivier d'Archambeau (O)

Department of Radiology, University Hospital Antwerp, Edegem, Belgium.

Judith de Vos-Geelen (J)

Department of Medical Oncology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht University, Maastricht, The Netherlands.

Jeroen Buijsen (J)

Departments of Radiation Oncology (MAASTRO), GROW School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, The Netherlands.

Christiaan van der Leij (C)

Departments of Radiology, Maastricht University Medical Center, Maastricht, The Netherlands.

Wilhelm den Toom (W)

Department of Radiotherapy, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.

Dave Sprengers (D)

Departments of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands.

Jan N M IJzermans (JNM)

Department of Surgery, Erasmus MC University Medical Center, Rotterdam, The Netherlands.

Adriaan Moelker (A)

Departments of Radiology and Nuclear Medicine, Erasmus MC University Medical Center, Rotterdam, The Netherlands.

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