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Updated: Feb 16, 2026

Treatment of Liver Metastases Using an Internal Target Volume Method for Stereotactic Body Radiotherapy
Published on: May 8, 2018
Initial clinical experience with stereotactic lung radiotherapy, based on a biological model-driven prescription
C Wesley Hodge1, Wolfgang A Tomé2,3, Tracy Weigel4
1Robert Boissoneault Oncology Institute, Ocala, FL 34471, Departments of.
A novel nomogram-based biological dose selection (NBDS) model for stereotactic body radiotherapy (SBRT) in early non-small cell lung cancer (NSCLC) demonstrated promising local control and survival rates. The model-predicted toxicity rates were consistent with observed outcomes, validating its potential for safe and effective treatment.
Area of Science:
- Oncology
- Radiotherapy
- Medical Physics
Background:
- Stereotactic body radiotherapy (SBRT) is a key treatment for early-stage non-small cell lung cancer (NSCLC).
- Accurate dose selection is crucial for balancing treatment efficacy and toxicity.
- Patient-specific biological dose selection models aim to optimize SBRT fractionation.
Purpose of the Study:
- To evaluate the initial clinical outcomes of SBRT for early-stage NSCLC using a patient-specific nomogram-based biological dose selection (NBDS) model.
- To assess the safety and efficacy of SBRT guided by the NBDS model in terms of local control, survival, and toxicity.
Main Methods:
- 23 patients with stage IA/B NSCLC received SBRT with a prescription isodose volume/residual lung volume ratio of 2-3%.
- Dose fractionation schemes were determined by the NBDS model to predict low rates of pneumonitis.
- Kaplan-Meier analysis was used to evaluate survival and local control; toxicity and response rates were also analyzed.
Main Results:
- Median follow-up was 43.2 months.
- 80% major response rate observed in 20 evaluable lesions.
- 3-year survival rates were 60% (overall), 79% (cause-specific), and 55% (disease-free).
- 3-year local control was 89%.
- Grade 2 or higher pulmonary toxicity occurred in 15-27% of patients, with grade 3 incidence at 4-10%.
Conclusions:
- SBRT utilizing an NBDS model achieved local control and survival rates comparable to higher-dose regimens.
- Observed pulmonary toxicity rates were within the model's predicted parameters.
- Further follow-up is required to confirm the long-term validity of the NBDS model.
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