Vienna, Austria

ESTRO 2023

Session Item

Monday
May 15
15:00 - 16:00
Business Suite 1-2
GI
Vincenzo Valentini, Italy
3410
Poster Discussion
Clinical
Definitive SBRT in early-stage HCC: an Australian multi-institutional review of outcomes
Howard Liu, Australia
PD-0896

Abstract

Definitive SBRT in early-stage HCC: an Australian multi-institutional review of outcomes
Authors:

Howard Liu1, Yoo Young Lee1, Swetha Sridharan2, Wei Wang3, Richard Khor4, Julie Chu5, Andrew Oar6, Ee Siang Choong7, Hien Le8, Mihir Shanker1, Alan Wigg9, Katherine Stuart10, David Pryor1

1Princess Alexandra Hospital, Radiation Oncology, Brisbane, Australia; 2Calvary Mater Newcastle, Radiation Oncology, Newcastle, Australia; 3The Crown Princess Mary Cancer Centre, Radiation Oncology, Sydney, Australia; 4 Olivia Newton-John Cancer Wellness and Research Centre, Radiation Oncology, Melbourne, Australia; 5Peter MacCallum Cancer Centre, Radiation Oncology, Melbourne, Australia; 6ICON Cancer Centre, Radiation Oncology, Gold Coast, Australia; 7Chris O'Brien Lifehouse, Radiation Oncology, Sydney, Australia; 8Royal Adelaide Hospital, Radiation Oncology, Adelaide, Australia; 9Flinders Medical Centre, Hepatology and Liver Transplantation Medicine Unit, Adelaide, Australia; 10Princess Alexandra Hospital, Department of Gastroenterology and Hepatology, Brisbane, Australia

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Purpose or Objective

Management of HCC is challenging as liver cirrhosis, comorbidities and tumor location can limit the choice of treatment modality. The majority of patients will be ineligible for resection or transplantation and several factors including tumor size and location impact on the feasibility and efficacy of thermal ablation or transarterial therapies. SBRT has demonstrated high rates of local control in multiple series, however, few studies have reported on SBRT specifically in the treatment naïve, curative intent setting.  We report the outcomes of patients with solitary early-stage HCC treated with SBRT as first line definitive therapy.

Material and Methods

This is a multi-institutional retrospective study between 2010 and 2019 of patients with a new diagnosis of BCLC stage 0/A HCC and a single ≤5cm lesion, Child-Pugh (CP) A compensated liver function who underwent SBRT as first line, curative intent therapy.  The primary end point was freedom from local progression (FFLP). Secondary end points were progression-free survival (PFS), overall survival (OS) and treatment related toxicity.

Results

68 patients met inclusion criteria with a median follow-up of 20 months (range, 3-58). Median age was 68 years (range, 50-86), 54 (79%) were male, 62 (91%) had cirrhosis and 50 (74%) patients were ECOG 0. The predominant etiologies of liver cirrhosis were NAFLD (48%), HCV (35%) and ALD (34%). Median HCC diameter was 2.6cm (range, 1.3-5) and serum AFP was 5.1 (range, 1.5-2275). Median prescription BED10 dose was 93Gy (range, 48-125Gy). The 2-year FFLP, PFS and OS were 94%, 60% and 88%, respectively. Two patients had local failures and did not undergo further treatment due to decline in general and hepatic function unrelated to SBRT. The predominant cause of disease progression was out-of-field intrahepatic relapse, occurring in 16 patients. Of those patients, 13 (81%) patients underwent additional liver directed therapy, 1 patient commenced systemic therapy and 2 patients received best supportive care in light of co-morbidities. Grade 2 and 3 clinical toxicity (excluding asymptomatic biochemical and hematological) was reported in 9 (13.2%) and 0 (0%) patients, respectively. A rise of ≥2 in CP-score was observed in six patients with cirrhosis (9.6%) within 3 months of SBRT.


Cohort characteristicsN=68

Gender

Male

Female


54

14

Age (years)

Median (range)

<60

≥60


68 (50 - 86)

8

60

Cirrhosis

Yes

No


62

6

Etiology

HCV

HBV

Alcohol liver disease

NAFLD

Other


22

6

21

30

5

ECOG

0

1

2

Not recorded


50

8

9

1

Child-Pugh Score

Non-cirrhotic

A5

A6


6

41

21

Baseline AFP

<20

≥20


54

14

Tumor size, cm

≤2

>2 - ≤5


20

48



Conclusion

SBRT is a well-tolerated, definitive first-line treatment option in patients with BCLC stage 0/A, single HCC with high rates of local control and warrants further study in the treatment naïve setting. The ongoing multicentre TROG 21-07 study is randomising non-surgical patients with solitary HCC ≤3cm to SBRT or thermal ablation and an additional “ablation ineligible” cohort with HCC ≤5cm to SBRT or transarterial therapies (ACTRN1262100144875).