Planning strategies for robust carbon-ion scanning radiotherapy for stage I esophageal cancer: a retrospective study

Author:

Suga Makito12,Kusano Yohsuke3,Takakusagi Yosuke4,Oosawa Yukio2,Minohara Shinichi3,Yoshida Daisaku4,Katoh Hiroyuki4,Kamada Tadashi4,Komori Masataka1

Affiliation:

1. Radiological and Medical Laboratory Sciences, Nagoya University Graduate School of Medicine , 1-1-20 Daiko-Minami, Higashi-ku, Nagoya City, Aichi, 461-8673 , Japan

2. Section of Radiation Therapy Technology, Kanagawa Cancer Center , 2-3-2 Nakao, Asahi-ku, Yokohama City, Kanagawa, 241-8515 , Japan

3. Section of Medical Physics and Engineering, Kanagawa Cancer Center , 2-3-2 Nakao, Asahi-ku, Yokohama City, Kanagawa, 241-8515 , Japan

4. Department of Radiation Oncology, Kanagawa Cancer Center , 2-3-2 Nakao, Asahi-ku, Yokohama City, Kanagawa, 241-8515 , Japan

Abstract

Abstract This study aimed to establish a treatment planning strategy with carbon-ion scanning radiotherapy (CIRTs) for stage I esophageal cancer. The clinical data of seven patients treated with CIRTs were used. The setup error and interfractional and intrafractional motion error were analyzed using in-room computed tomography (CT) images for each treatment day. Finally, the planning target volume (PTV) margin was identified according to the accuracy of the treatment system. To ensure robustness against the positional displacements of the target and organs at risk (OAR), the replacement areas were placed as a contour adjacent to the tumor or OAR on the CT-image. The CT values of these areas were replaced by those of the target or OAR. Further, the dose distributions were optimized. Moreover, the variations in the target coverage from the initial plan for each treatment day (ΔV95%) were evaluated. By contrast, the risk of OAR was not evaluated in this study. The setup error was within 1.0 mm. The interfractional and intrafractional target motion errors were 2.8 and 5.0 mm, respectively. The PTV margins were 6.5 and 6.8 mm in the axial and depth directions, respectively. The robustness to target and OAR displacement was evaluated. The results showed that the target coverage with replacement could suppress decreased target coverage more than that without replacement. The PTV determination and replacement methods used in this study improved the target coverage in CIRTs for stage I esophageal cancer. Despite the need for a clinical follow-up, this method may help to improve clinical outcomes.

Funder

Toshiba Energy Systems and Solutions Corporation

Publisher

Oxford University Press (OUP)

Subject

Health, Toxicology and Mutagenesis,Radiology, Nuclear Medicine and imaging,Radiation

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