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Optimal Stereotactic Body Radiotherapy Dosage For Hepatocellular Carcinoma
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Abstract
Background and purpose
The optimal dose and fractionation scheme of stereotactic body radiation therapy (SBRT) for hepatocellular carcinoma (HCC) remains unclear due to different tolerated liver volumes and degrees of cirrhosis. We compared the effectiveness of stereotactic body radiation therapy dosing regimens for hepatocellular carcinoma (HCC).
Methods and materials
This single-center retrospective study included 604 patients treated during 2011-2017. Biologically effective dose (BED
10
) and equivalent dose in 2 Gym fractions (EQD
2
) were assumed at an α/β ratio of 10. Overall survival (OS), local recurrence-free rate (LRF), intrahepatic recurrence-free rate (IRF), and progression-free survival (PFS) was evaluated in univariable and propensity-score matched analyses.
Results
Median tumor size was 5.2 cm (interquartile range [IQR], 1.1-21.0). Median follow-up was 31 months in surviving patients (IQR, 3-82). High radiotherapy dose correlated with better OS, PFS, LRF and IRF. Different post-SBRT OS, PFS, LRF and IRF rates were observed for stereotactic ablative radiotherapy (SART) with BED
10
≥100 Gy, SBRT with EQD
2
≥74 Gy to BED
10
<100 Gy, and stereotactic conservative radiotherapy (SCRT) with EQD
2
<74 Gy.
Conclusions
High radiotherapy dose correlated with better outcomes. If tolerated by normal tissue, we recommend SART as a first-line ablative dose or SBRT as a second-line radical dose. Otherwise, SCRT is recommended as palliative irradiation.
Title: Optimal Stereotactic Body Radiotherapy Dosage For Hepatocellular Carcinoma
Description:
Abstract
Background and purpose
The optimal dose and fractionation scheme of stereotactic body radiation therapy (SBRT) for hepatocellular carcinoma (HCC) remains unclear due to different tolerated liver volumes and degrees of cirrhosis.
We compared the effectiveness of stereotactic body radiation therapy dosing regimens for hepatocellular carcinoma (HCC).
Methods and materials
This single-center retrospective study included 604 patients treated during 2011-2017.
Biologically effective dose (BED
10
) and equivalent dose in 2 Gym fractions (EQD
2
) were assumed at an α/β ratio of 10.
Overall survival (OS), local recurrence-free rate (LRF), intrahepatic recurrence-free rate (IRF), and progression-free survival (PFS) was evaluated in univariable and propensity-score matched analyses.
Results
Median tumor size was 5.
2 cm (interquartile range [IQR], 1.
1-21.
0).
Median follow-up was 31 months in surviving patients (IQR, 3-82).
High radiotherapy dose correlated with better OS, PFS, LRF and IRF.
Different post-SBRT OS, PFS, LRF and IRF rates were observed for stereotactic ablative radiotherapy (SART) with BED
10
≥100 Gy, SBRT with EQD
2
≥74 Gy to BED
10
<100 Gy, and stereotactic conservative radiotherapy (SCRT) with EQD
2
<74 Gy.
Conclusions
High radiotherapy dose correlated with better outcomes.
If tolerated by normal tissue, we recommend SART as a first-line ablative dose or SBRT as a second-line radical dose.
Otherwise, SCRT is recommended as palliative irradiation.
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