Microdosimetric evaluation of a clinical carbon ion beam using a tissue-equivalent proportional counter.

Abstract

Microdosimetry provides critical insights into radiation quality and relative biological effectiveness (RBE) in carbon ion therapy. However, its application in modern pulsed scanning beams is limited due to detector response challenges at high dose rates. This study evaluates the feasibility of using a commercially available spherical tissue-equivalent proportional counter (TEPC) (LET-1/2, Far West Technologies) to measure microdosimetric spectra in a clinical carbon ion beam, comparing results with Monte Carlo simulations. Microdosimetric measurements were performed at the National Center for Oncological Hadrontherapy (CNAO) using the LET-1/2 filled with 33.1 mmHg tissue-equivalent gas to simulate a 1 µm diameter tissue volume. Measurements were conducted at various depths and beam energies, covering a range of LETs. Data were processed to obtain frequency- and dose-weighted lineal energy distributions, from which saturation-corrected dose-mean lineal energy values and RBE calculated with the modified microdosimetric kinetic model were derived. Monte Carlo simulations using TOPAS replicated the experimental setup for comparison. TEPC measurements demonstrated reasonable agreement with Monte Carlo simulations when the beam intensity was sufficiently reduced to mitigate pulse pileup. At the standard clinical beam intensity, microdosimetric spectra exhibited distortions due to pulse pileup effects, leading to overestimation of high lineal energy events. However, when the lowest-intensity synchrotron mode was used to achieve reduced beam intensities (~1.5×10⁵ particles/s), agreement between measured and simulated spectra improved significantly, with RBE values derived from the measured spectra agreeing with Monte Carlo predictions to <4%. Background subtraction techniques and repeatability analyses confirmed the robustness of the TEPC measurements under optimized conditions. This study establishes conditions under which a TEPC can reliably measure microdosimetric spectra in pulsed carbon ion beams. These findings support its potential for clinical applications, including treatment verification and quality assurance in carbon ion therapy. The results contribute to ongoing efforts in RBE assessment and credentialing for clinical trials.