Phase I Study of Carbon Ion Radiotherapy and Image-Guided Brachytherapy for Locally Advanced Cervical Cancer

  • Yuya Yoshimoto
    Gunma University Heavy Ion Medical Center, Gunma University, 3-39-22 Showa, Maebashi, Gunma 371-8511, Japan
  • Noriyuki Okonogi
    Gunma University Heavy Ion Medical Center, Gunma University, 3-39-22 Showa, Maebashi, Gunma 371-8511, Japan
  • Ken Ando
    Gunma University Heavy Ion Medical Center, Gunma University, 3-39-22 Showa, Maebashi, Gunma 371-8511, Japan
  • Tomoaki Tamaki
    Gunma University Heavy Ion Medical Center, Gunma University, 3-39-22 Showa, Maebashi, Gunma 371-8511, Japan
  • Shingo Kato
    Department of Radiation Oncology, Saitama Medical University International Medical Center, 1397-1 Yamane, Hidaka, Saitama 350-1298, Japan
  • Takashi Hirakawa
    Department of Obstetrics and Gynecology, Gunma University Graduate School of Medicine, 3-39-22 Showa, Maebashi, Gunma 371-8511, Japan
  • Kazutoshi Murata
    Gunma University Heavy Ion Medical Center, Gunma University, 3-39-22 Showa, Maebashi, Gunma 371-8511, Japan
  • Tatsuya Kanuma
    Division of Gynecology, Gunma Prefectural Cancer Center, 617-1 Takahayashi-nishi, Ota, Gunma 373-0828, Japan
  • Takashi Minegishi
    Department of Obstetrics and Gynecology, Gunma University Graduate School of Medicine, 3-39-22 Showa, Maebashi, Gunma 371-8511, Japan
  • Takashi Nakano
    Gunma University Heavy Ion Medical Center, Gunma University, 3-39-22 Showa, Maebashi, Gunma 371-8511, Japan
  • Tatsuya Ohno
    Gunma University Heavy Ion Medical Center, Gunma University, 3-39-22 Showa, Maebashi, Gunma 371-8511, Japan
  • Shin-ei Noda
    Gunma University Heavy Ion Medical Center, Gunma University, 3-39-22 Showa, Maebashi, Gunma 371-8511, Japan

書誌事項

公開日
2018-09-18
資源種別
journal article
権利情報
  • https://creativecommons.org/licenses/by/4.0/
DOI
  • 10.3390/cancers10090338
公開者
MDPI AG

説明

<jats:p>A phase I study was performed to determine the recommended dose of carbon ion radiotherapy and 3D image-guided brachytherapy for histologically confirmed stage II (≥4 cm), III, or IVA cervical cancer. Dose-limiting toxicities (treatment-related toxicities occurring within three months from the start of carbon ion radiotherapy) included Grade 3 non-hematological toxicity, Grade 4 hematological toxicity, or interruption of treatment for more than two weeks due to treatment-related toxicities. Carbon ion radiotherapy consisted of whole-pelvic irradiation with 36.0 Gy (relative biological effectiveness) in 12 fractions and local boost with 19.2 Gy in four fractions for the primary site, and for positive lymph nodes. Three sessions of three-dimensional (3D) image-guided brachytherapy were administered after completion of carbon ion radiotherapy. Weekly cisplatin at a dose of 40 mg/m2 was given concurrently. At a dose level of one, a total rectosigmoid D2cc dose between 67.2 Gy and 71.3 Gy at a biological equivalent dose of 2 Gy per fraction from carbon ion radiotherapy and 3D image-guided brachytherapy was prescribed. Six patients were enrolled into this dose level. No patients developed the pre-defined dose-limiting toxicities. For late toxicities, however, one patient developed Grade 3 rectal hemorrhage requiring transfusion at 10 months after treatment. The median survival time was 50.0 months for the five surviving patients. No further dose escalation was performed, and we determined the dose of level one as the recommended rectosigmoid dose. Although our results are preliminary, the study regimen encourages further investigation (registration: UMIN000013340).</jats:p>

収録刊行物

  • Cancers

    Cancers 10 (9), 338-, 2018-09-18

    MDPI AG

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参考文献 (32)*注記

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