Stereotactic Body Radiotherapy for Small Unresectable Hepatocellular Carcinomas.


Journal

Clinical oncology (Royal College of Radiologists (Great Britain))
ISSN: 1433-2981
Titre abrégé: Clin Oncol (R Coll Radiol)
Pays: England
ID NLM: 9002902

Informations de publication

Date de publication:
06 2019
Historique:
received: 17 06 2018
revised: 08 01 2019
accepted: 08 01 2019
pubmed: 23 2 2019
medline: 15 4 2020
entrez: 23 2 2019
Statut: ppublish

Résumé

Stereotactic body radiotherapy (SBRT) is an option for the treatment of hepatocellular carcinoma (HCC) in patients ineligible for standard local therapies. This study reports on the safety and efficacy of SBRT in small HCC tumours (≤5 cm) in the province of British Columbia. Between March 2011 and July 2015, 31 patients with Child-Pugh Class A or B, with small HCCs measuring ≤5 cm were treated with SBRT at our institution. Primary end points were local control, progression-free survival, overall survival and toxicity. Thirty-four hepatomas (median size 3.3 cm, range 1.3-5.0 cm) were treated. The median follow-up was 18.3 months. Twenty-six patients (84%) had received previous liver-directed treatments. Most patients (88%) were treated with 45 Gy in three or five fractions. Six patients (19%) had worsened Child-Pugh score by two or more points during follow-up; overall 32% of patients experienced ≥ grade 3 + toxicities. One-year local control and overall survival were 94 and 84%, respectively. One-year progression-free survival was 49%; 81% of patients with disease progression received further HCC therapy. On univariate analysis, small tumour size predicted for improved overall survival (P = 0.01) whereas prescription biological equivalent dose (BED SBRT provides high local control to small inoperable HCC. SBRT can be delivered safely even after previous liver-directed therapies and further liver therapies can follow treatment with SBRT. Although overall 32% of patients experienced ≥ grade 3 + toxicities, and 19% had a deterioration in Child-Pugh score of two or more points, these changes were mainly transient with minimal clinical impact. Despite excellent local control, disease progression outside of the irradiated site remains prominent. Further studies are warranted to examine combined therapy approaches to maximise disease control.

Identifiants

pubmed: 30792051
pii: S0936-6555(19)30051-2
doi: 10.1016/j.clon.2019.01.012
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

365-373

Informations de copyright

Copyright © 2019. Published by Elsevier Ltd.

Auteurs

R Yeung (R)

Halvorson Cancer Center, Evergreen Health Medical Center, Kirkland, Washington, USA.

L Beaton (L)

Department of Radiation Oncology, British Columbia Cancer Agency, Vancouver Center, Vancouver, British Columbia, Canada.

T Rackley (T)

Department of Radiation Oncology, British Columbia Cancer Agency, Vancouver Center, Vancouver, British Columbia, Canada.

B Weber (B)

Department of Radiation Oncology, British Columbia Cancer Agency, Vancouver Center, Vancouver, British Columbia, Canada.

J Hamm (J)

Cancer Surveillance and Outcomes, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.

R Lee (R)

Department of Medical Physics, British Columbia Cancer Agency, Vancouver Center, Vancouver, British Columbia, Canada.

M Camborde (M)

Department of Medical Physics, British Columbia Cancer Agency, Vancouver Center, Vancouver, British Columbia, Canada.

M Pearson (M)

Department of Medical Physics, British Columbia Cancer Agency, Vancouver Center, Vancouver, British Columbia, Canada.

C Duzenli (C)

Department of Medical Physics, British Columbia Cancer Agency, Vancouver Center, Vancouver, British Columbia, Canada.

S K Loewen (SK)

Department of Radiation Oncology, Tom Baker Cancer Center, Calgary, Alberta, Canada.

M Liu (M)

Department of Radiation Oncology, British Columbia Cancer Agency, Vancouver Center, Vancouver, British Columbia, Canada.

R Ma (R)

Department of Radiation Oncology, British Columbia Cancer Agency, Vancouver Center, Vancouver, British Columbia, Canada.

D Schellenberg (D)

Department of Radiation Oncology, British Columbia Cancer Agency, Vancouver Center, Vancouver, British Columbia, Canada. Electronic address: dschellenberg@bccancer.bc.ca.

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Classifications MeSH