Fiducial marker matching versus vertebral body matching: Dosimetric impact of patient positioning in carbon ion radiotherapy for primary hepatic cancer
Fiducial marker matching versus vertebral body matching: Dosimetric impact of patient positioning in carbon ion radiotherapy for primary hepatic cancer
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DOI:
10.1016/j.ejmp.2016.12.018
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发表时间:
2017-01-01
影响因子:
3.4
通讯作者:
Nakano, Takashi
中科院分区:
文献类型:
--
作者:
Abe, Satoshi;Kubota, Yoshiki;Nakano, Takashi
Purpose: The aim of this study was to compare the dose-volume parameters of fiducial marker matching (MM) with vertebral body matching (VM) in patient positioning for carbon ion radiotherapy for primary hepatic cancer.Materials and methods: Twenty patients with primary hepatic cancer were retrospectively studied to assess changes in reproducibility of tumor position and dose distribution on two CT scans. One was for treatment planning and another was for dose confirmation, acquired the day before the first treatment day. The coverage of the clinical target volume (CTV) (D-98) and normal liver volume excluding the CTV which received 20 Gy relative biological effectiveness (RBE) (V-20) were used as evaluation parameters. Additionally, the correlation of tumor movement and D98 was calculated in VM and MM. The prescription dose was 60.0 Gy (RBE) delivered in four fractions (15 Gy/fx).Results: The median (range) D-98 for VM and MM was 57.9 (20.8-59.9) and 59.9 (57.2-60.3) Gy (RBE), respectively. The median (range) V-20 for VM and MM was 17.9 (4.8-44.4) and 16.2 (4.7-44.9) Gy (RBE), respectively. The D-98 for MM was significantly larger than that for VM (p = 0.001), although V-20 showed no significant difference (p > 0.05). Twelve patients were clinically acceptable (D-98 > 57 Gy (RBE)) with VM, while all patients were clinically acceptable with MM. Marker movement correlated with a decrease of D-98 for VM (R = -0.814).Conclusion: Compared with VM, MM was clinically acceptable in all patients. This suggests that MM is more robust than VM. (C) 2016 Associazione Italiana di Fisica Medica. Published by Elsevier Ltd.