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A Comparative Dosimetric Study of Proton and Photon Therapy in Stereotactic Arrhythmia Radioablation for Ventricular Tachycardia

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Journal ArXiv
Date 2025 Feb 20
PMID 39975428
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Abstract

Purpose: Ventricular tachycardia (VT) is a life-threatening arrhythmia commonly treated with catheter ablation; however, some cases remain refractory to conventional treatment. Stereotactic arrhythmia radioablation (STAR) has emerged as a non-invasive option for such patients. While photon-based STAR has shown efficacy, proton therapy offers potential advantages due to its superior dose conformity and sparing of critical organs at risk (OARs), including the heart itself. This study aims to investigate and compare the dosimetry between proton and photon therapy for VT, focusing on target coverage and OAR sparing.

Methods: We performed a retrospective study on a cohort of 34 VT patients who received photon STAR. Proton STAR plans were generated using robust optimization in RayStation to deliver the same prescription dose of 25 Gy in a single fraction while minimizing dose to OARs. Dosimetric metrics, including D, D, D, and D, were extracted for critical OARs (heart, lungs, esophagus) and ventricular arrhythmogenic substrates (VAS). Shapiro-Wilk tests were used to assess normality, followed by paired t-tests or Wilcoxon signed-rank tests for statistical comparisons between modalities, with Bonferroni correction applied for multiple comparisons.

Results: Proton and photon plans achieved comparable target coverage, with VAS D of 24.1 ± 1.2 Gy vs. 24.7 ± 1.0 Gy (p=0.294). Proton therapy significantly reduced OAR doses, including heart D (3.6 ± 1.5 Gy vs. 5.5 ± 2.0 Gy, p<0.001), lungs D (1.6 ± 1.5 Gy vs. 2.1 ± 1.4 Gy, p<0.001), and esophagus D (0.3 ± 0.6 Gy vs. 1.6 ± 1.3 Gy, p<0.001), while maintaining optimal target coverage.

Conclusion: Proton therapy for STAR demonstrates significant dosimetric advantages in sparing the heart and other critical OARs compared to photon therapy for VT, while maintaining equivalent target coverage. These findings highlight the potential of proton therapy to reduce treatment-related toxicity and improve outcomes for VT patients.

References
1.
Paganetti H . Mechanisms and Review of Clinical Evidence of Variations in Relative Biological Effectiveness in Proton Therapy. Int J Radiat Oncol Biol Phys. 2021; 112(1):222-236. PMC: 8688199. DOI: 10.1016/j.ijrobp.2021.08.015. View

2.
Lerman B . Mechanism, diagnosis, and treatment of outflow tract tachycardia. Nat Rev Cardiol. 2015; 12(10):597-608. DOI: 10.1038/nrcardio.2015.121. View

3.
Pouvreau P, Taleb I, Fontaine A, Edouard L, Gibson N, Yaouanq M . Heart is a heavy burden: cardiac toxicity in radiation oncology. Support Care Cancer. 2024; 32(11):769. DOI: 10.1007/s00520-024-08949-7. View

4.
Zou Z, Bowen S, Thomas H, Sasidharan B, Rengan R, Zeng J . Scanning Beam Proton Therapy versus Photon IMRT for Stage III Lung Cancer: Comparison of Dosimetry, Toxicity, and Outcomes. Adv Radiat Oncol. 2020; 5(3):434-443. PMC: 7276696. DOI: 10.1016/j.adro.2020.03.001. View

5.
Chan M, Parikh D, Shi C . Narrative Review: Cardiotoxicities and Cardiac-Sparing Techniques in Radiotherapy. Technol Cancer Res Treat. 2024; 23:15330338241301211. PMC: 11622324. DOI: 10.1177/15330338241301211. View