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Radiation-induced secondary malignancies for nasopharyngeal carcinoma: A pilot study of patients treated via IMRT or VMAT

  • Hsiao Fei Lee
  • , Jen Hong Lan
  • , Pei Ju Chao
  • , Hui Min Ting
  • , Hui Chun Chen
  • , Hsuan Chih Hsu*
  • , Tsair Fwu Lee
  • *此作品的通信作者
  • National Kaohsiung University of Science and Technology
  • Chang Gung University
  • Kaohsiung Medical University
  • Yuan's General Hospital

研究成果: 期刊稿件 › 文章 › 同行評審

20 引文 斯高帕斯(Scopus)

摘要

Background: Patients treated with radiotherapy are at risk of developing a second cancer during their lifetime, which can directly impact treatment decision-making and patient management. The aim of this study was to qualify and compare the secondary cancer risk (SCR) after intensity-modulated radiation therapy (IMRT) and volumetric-modulated arc therapy (VMAT) in nasopharyngeal carcinoma (NPC) patients. Patients and methods: We analyzed the treatment plans of a cohort of 10 NPC patients originally treated with IMRT or VMAT. Dose distributions in these plans were used to calculate the organ equivalent dose (OED) with Schneider’s full model. Analyses were applied to the brain stem, spinal cord, oral cavity, pharynx, parotid glands, lung, mandible, healthy tissue, and planning target volume. Results: We observed that the OED-based risks of SCR were slightly higher for the oral cavity and mandible when VMAT was used. No significant difference was found in terms of the doses to other organs, including the brain stem, parotids, pharynx, submandibular gland, lung, spinal cord, and healthy tissue. In the NPC cohort, the lungs were the organs that were most sensitive to radiation-induced cancer. Conclusion: VMAT afforded superior results in terms of organ-at-risk-sparing compared with IMRT. Most OED-based second cancer risks for various organs were similar when VMAT and IMRT were employed, but the risks for the oral cavity and mandible were slightly higher when VMAT was used.

原文英語
頁(從 - 到)131-141
頁數11
期刊Cancer Management and Research
卷10
DOIs
出版狀態已出版 - 2018

文獻附註

Publisher Copyright:
© 2018 Lee et al.

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