Feasibility and potential clinical benefit of dose de-escalation in stereotactic ablative radiotherapy for lung cancer lesions with ground glass opacities
Treatment of neoplasic lung nodules with ground glass opacities (GGO) faces two primary challenges. First, the standard practice of treating GGOs as solid nodules, which effectively controls the tumor locally, but might increase associated toxicities. The second is the potential for dose calculation...
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Veröffentlicht in: | Physics and imaging in radiation oncology 2024-10, Vol.32, p.100681, Article 100681 |
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Sprache: | eng |
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Zusammenfassung: | Treatment of neoplasic lung nodules with ground glass opacities (GGO) faces two primary challenges. First, the standard practice of treating GGOs as solid nodules, which effectively controls the tumor locally, but might increase associated toxicities. The second is the potential for dose calculation errors related to increased heterogeneity. This study addresses the optimization of a dose de-escalation regime for stereotactic ablative radiotherapy (SABR) for GGO lesions.
We used the CT scans of 35 patients (40 lesions) with some degree of GGO component treated at our institution between 2017 and 2021. We first assessed the dose calculation accuracy as a function of the GGO component of the lesion. We then analysed the advantages of a dose de-escalation regime in terms of lung dose reduction (Dmean, V20Gy and V300GyBED3) and plan robustness.
We found a positive correlation between the presence of GGO and the dose calculation errors in a phantom scenario. These differences are reduced for patient data and in the presence of breathing motion. When using a de-escalation regime, significant reductions were achieved in mean lung dose, V20Gy and V300GyBED3. This study also revealed that lower doses in GGO areas lead to more stable fluence patterns, increasing treatment robustness.
The study lays the foundation for an eventual use of dose de-escalation in SABR for treating lung lesions with GGO, potentially leading to equivalent local control while reducing associated toxicities. These findings lay the groundwork for future clinical trials. |
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ISSN: | 2405-6316 2405-6316 |
DOI: | 10.1016/j.phro.2024.100681 |