Monte Carlo simulations show increased biological effectiveness of nitrogen-targeted proton therapy with carbon and alpha particles, suggesting improved treatment outcomes.
Proton therapy has been criticized due to its relatively low biological effectiveness compared with heavy particle therapy, for example, 12C ion therapy. Recently, we proposed a new strategy for proton therapy to improve biological effectiveness, termed as nitrogen-targeting-Proton-Carbon-Alpha-Therapy (Proton-CAT). The previous work has demonstrated its feasibility to enhance the yield of high-linear energy transfer (LET) particles with a monoenergetic proton beam. To assess the feasibility of Proton-CAT for spread-out Bragg peak (SOBP) beams, we employed Monte Carlo simulations at both macroscopic and microscopic levels. For macroscopic calculations, an SOBP of 24–32 MeV protons with a modulation width of 3.0 mm was constructed and irradiated into a tissue-equivalent phantom with and without 15N material (10% and 30% 15N concentration). Dose deposition by protons, alpha particles, and 12C ions was scored along the beam path. For microscopic evaluation, a cell model was used to assess the damage inflicted by energetic particles (12C ions and α-particles). The results demonstrated the advantages of the Proton-CAT. Within the SOBP (0.6–0.82 cm depth), the average dose amplification for 12C ions exceeded 15.8% (10% 15N) and 38.5% (30% 15N), while for α-particles, it surpassed 68.5% (10% 15N) and 203.8% (30% 15N). Moreover, the energy deposition of 12C ions and α-particles in cell nucleus reached up to 3.50 keV μm−3 (10% and 30% 15N concentration). These findings support the hypothesis that the Proton-CAT has the feasibility to yield short-range, high-LET 12C ions and α-particles within the SOBP region.
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Wu et al. (2026) studied this question.
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