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Updated: Apr 17, 2026

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Treatment of Liver Metastases Using an Internal Target Volume Method for Stereotactic Body Radiotherapy
Published on: May 8, 2018
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Neoadjuvant Stereotactic Body Radiotherapy plus Immune Therapy Favorably Remodels the Hepatocellular Carcinoma Tumor
Zoe Cosner1, Zhoubo Guo2,3, Cole Nawrocki4
1Department of Radiation Oncology, Massachusetts General Brigham Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Summary
Neoadjuvant stereotactic body radiation therapy (SBRT) combined with immunotherapy shows promise for early-stage liver cancer. This approach is safe and enhances anti-cancer immune responses, warranting further clinical investigation.
Area of Science:
- Hepatobiliary Oncology
- Radiation Oncology
- Immunotherapy
Background:
- Advanced hepatocellular carcinoma (HCC) treatment has improved with immunotherapy, but its use in earlier stages needs definition.
- Optimal sequencing of therapies for resectable HCC remains an area of active research.
Purpose of the Study:
- To evaluate the safety and efficacy of neoadjuvant stereotactic body radiation therapy (SBRT) followed by atezolizumab and bevacizumab in patients with initially resectable HCC.
- To investigate the impact of this neoadjuvant regimen on the tumor immune microenvironment.
Main Methods:
- A single-arm pilot study enrolled 8 patients with resectable HCC.
- Patients received neoadjuvant SBRT, two cycles of atezolizumab plus bevacizumab, and then surgical resection.
- Safety was assessed by grade 3-4 treatment-related adverse events (trAEs), and tumor immune microenvironment changes were analyzed using spatial transcriptomics.
Main Results:
- The regimen was safe, with only one patient experiencing a grade 3 trAE.
- Seven of eight patients underwent successful R0 resection.
- Post-treatment tumors showed increased anti-cancer immune infiltration, correlating with radiographic response.
Conclusions:
- Neoadjuvant SBRT and immunotherapy is a safe strategy for resectable HCC.
- This approach enhances anti-cancer immunity and provides a rationale for further clinical trials.
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