Main Session
Sep
29
PQA 05 - Physics
3025 - Comparative Dosimetric Analysis of Dynamic Collimator VMAT (DC-VMAT) Static Angle Modulated Port (STAMP) Optimization Strategies vs. VMAT for Breast Radiotherapy with Regional Nodal Irradiation
Presenter(s)
Cheukkai Hui, PhD - Kaiser Permanente - Dublin, Dublin, CA
P. Kaur, D. L. Saenz, C. H. Chapman, Y. D. Mutaf, and C. B. Hui; Kaiser Permanente, Dublin, CA
Purpose/Objective(s):
This study compares three Dynamic Collimator VMAT (DC-VMAT) Static Angle Modulated Port (STAMP) optimization strategies with varying control point (CP) counts against conventional VMAT, assessing effects on breast radiotherapy plan quality and delivery.Materials/Methods:
Thirty breast cancer patient datasets receiving regional nodal irradiation were retrospectively selected. For each patient, one VMAT and three DC-VMAT plans with dynamic collimator were generated: arc-dominant (AD: 2 CP; 1 STAMP), balanced (BAL: 26 CP; 4 STAMP), and static-dominant (SD: 51 CP; 4 STAMP). All plans used two arcs and were optimized with identical target and OAR constraints. Prescription was 4005cGy in 15 fractions, normalized so 95% of breast PTV received 95% of the dose. Seven clinically relevant OAR metrics were evaluated to compare plan quality.Results:
Hotelling’s T² tests showed significant differences between VMAT and all DC-VMAT strategies (p < 0.0001). All DC-VMAT plans maintained clinically acceptable nodal coverage and reduced all seven OAR metrics vs VMAT (p < 0.0001), with increased MU/dose reflecting a reduction in delivery efficiency (Table 1). BAL and SD were statistically equivalent across all OAR metrics (p > 0.1). Compared with these higher-CP strategies, AD yielded equivalent ipsilateral lung Dmean and contralateral lung V400 (p > 0.1), slightly lower ipsilateral lung V1600, and higher for the remaining four OAR metrics (p < 0.05).Conclusion:
DC-VMAT techniques for breast radiotherapy significantly reduce heart, contralateral breast, and lung doses compared with VMAT while maintaining target coverage. These reductions are expected to decrease long-term cardiac risk and the likelihood of radiation-induced pulmonary toxicity, while lowering exposure to contralateral breast and lung, potentially minimizing secondary malignancy risks. Although dosimetric differences among DC-VMAT strategies were relatively small, higher CP approaches (BAL and SD) provided incremental improvements in specific metrics. The primary dose reduction is attributable to the rotating collimation DC-VMAT technique, while the additional STAMPs further enhance sparing, particularly for heart and contralateral breast. Despite slightly higher MU and longer delivery times, DC-VMAT offers a viable improvement in plan quality over VMAT, offering superior OAR sparing in breast radiotherapy. Table 1. Average OAR metrics| VMAT | AD | BAL | SD | |
| Breast Contra Dmean (cGy) | 380 | 213 | 206 | 208 |
| Lung Ipsi Dmean (cGy) | 1085 | 954 | 958 | 962 |
| Lung Ipsi V1600 (%) | 25.5 | 21.2 | 21.8 | 22.0 |
| Lung Ipsi V400 (%) | 67.0 | 59.0 | 57.2 | 57.1 |
| Lung Contra Dmean (cGy) | 278 | 195 | 188 | 187 |
| Lung Contra V400 (%) | 22.1 | 10.7 | 10.2 | 10.1 |
| Heart Dmean (cGy) | 270 | 201 | 196 | 194 |
| MU/Dose Ratio | 2.89 | 3.61 | 3.73 | 4.26 |
| Delivery Time (min) | 1.43 | 1.87 | 2.08 | 2.47 |