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SBRT with ≥70 Gy BED10 for colorectal liver metastases shows 74.5% 1-year FFLPCan a higher radiation dose improve tumor control in liver metastases?

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Key Takeaway
Consider that higher PTV Dmin during SBRT for colorectal liver metastases may be associated with improved local control, but evidence is observational.

This was a retrospective, single-institution cohort study of 116 patients with 128 colorectal liver metastases treated with stereotactic body radiation therapy (SBRT) using a biologically effective dose (BED10) of ≥70 Gy. The median follow-up was 22.3 months. There was no reported comparator group.

The primary outcome was freedom from local progression (FFLP). The 1-year FFLP rate was 74.5%, and the 2-year FFLP rate was 58.8%. On multivariable analysis, a higher minimum planning target volume (PTV) dose was associated with improved FFLP (HR 0.89 per 10 Gy BED10, 95% CI 0.83–0.96, p = 0.002). Polymetastatic disease was associated with worse FFLP (HR 3.31, 95% CI 1.79–6.12, p < 0.001). When stratified by a PTV Dmin cut-point of 100 Gy BED10, the 1-year FFLP was 64.2% for low dose versus 87.1% for high dose (p < 0.001).

Safety and tolerability data were not reported. Key limitations include the retrospective, single-institution design and the absence of a comparator group. The practice relevance suggests that incorporating PTV Dmin into SBRT planning may improve FFLP beyond the nominal prescription dose. However, this is an observational study; associations do not imply causation, and findings are limited by study design.

If you or someone you love has colorectal cancer that has spread to the liver, keeping those tumors under control is a huge worry. This study looked at 116 patients with 128 liver metastases who received a high-dose radiation treatment called stereotactic body radiation therapy (SBRT). The main question was whether a higher minimum dose to the tumor would help keep it from growing back locally.

Over a median follow-up of about 22 months, the one-year rate of the tumor not growing locally was 74.5%, and the two-year rate was 58.8%. The researchers found that a higher minimum dose to the planning target volume (the area planned for radiation) was linked to better tumor control. Specifically, for every 10-unit increase in the dose, the risk of the tumor growing back dropped by about 11%. Patients with multiple tumors in the liver had a much higher risk of the tumor growing back.

This was a retrospective study from a single institution, meaning it looked back at past patients without a comparison group getting a different treatment. No safety issues were reported, but the study did not track side effects. Because it's observational, we can't say the higher dose caused the better control—it's just an association.

The findings suggest that planning radiation to ensure a higher minimum dose to the tumor might help, but the results are limited by the study's design and can't be generalized to all patients.

What this means for you:
A higher minimum radiation dose to liver tumors may help control them, but this is early, observational evidence.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
BackgroundThis single-institution retrospective study investigated whether actual dosimetric plan quality metrics better predict freedom from local progression (FFLP) than nominal prescription dose after stereotactic body radiation therapy (SBRT) for colorectal liver metastases (CLM).MethodsA total of 116 patients with 128 CLM treated with SBRT (≥70 Gy biologically effective dose [BED10]) were retrospectively analyzed. Clinical variables and dosimetric factors, including maximum, minimum, and mean doses (Dmax, Dmin, Dmean), as well as dose to x% of the planning target volume (PTV) (Dx%), were evaluated. Cox regression analyses and the Akaike information criterion were used to identify prognostic factors for FFLP.ResultsWith a median follow-up of 22.3 months, 1-year and 2-year FFLP rates were 74.5% and 58.8%, respectively. On univariable analyses, extent of metastasis, number of systemic therapy lines, pre- and post-SBRT carcinoembryonic antigen, PTV, prescription dose, and other plan parameters (Dmax, Dmin, Dmean, D2%, D95%, D98%, D99%) were significant. In the final multivariable model, PTV Dmin (HR 0.89 per 10 Gy BED10, 95% CI 0.83–0.96, p = 0.002) and polymetastatic disease (HR 3.31, 95% CI 1.79–6.12, p < 0.001) independently predicted FFLP. Using an optimal cut-point of 100 Gy BED10, low-PTV Dmin was associated with inferior FFLP compared with high-PTV Dmin (1-year: 64.2% vs. 87.1%, p < 0.001).ConclusionPTV Dmin emerged as the most robust dosimetric predictor of FFLP. Incorporating PTV Dmin into SBRT planning may improve FFLP beyond nominal prescription dose.
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