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Single-arm confirmatory trial of postoperative concurrent chemoradiotherapy using intensity modulated radiation therapy for patients with high-risk uterine cervical cancer: Japan Clinical Oncology Group study (JCOG1402).
Murakami, Naoya; Isohashi, Fumiaki; Hasumi, Yoko; Kasamatsu, Takahiro; Okamoto, Hiroyuki; Nakamura, Kenichi; Shibata, Taro; Ito, Yoshinori; Ishikura, Satoshi; Nishimura, Yasumasa; Yaegashi, Nobuo; Toita, Takafumi.
Afiliación
  • Murakami N; Department of Radiation Oncology, National Cancer Center Hospital, Tsukiji 5-1-1, Chuo-ku, Tokyo, Japan.
  • Isohashi F; Department of Radiation Oncology, Osaka University Graduate School of Medicine, Osaka, Japan.
  • Hasumi Y; Department of Obstetrics and Gynecology, Mitsui Memorial Hospital, Tokyo, Japan.
  • Kasamatsu T; Department of Obstetrics and Gynecology, Tokyo Metropolitan Bokutoh Hospital, Tokyo, Japan.
  • Okamoto H; Department of Medical Physics, National Cancer Center Hospital, Tokyo, Japan.
  • Nakamura K; Japan Clinical Oncology Group Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.
  • Shibata T; Japan Clinical Oncology Group Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.
  • Ito Y; Department of Radiation Oncology, Showa University School of Medicine, Tokyo, Japan.
  • Ishikura S; Department of Radiology, Nagoya City University Graduate School of Medical Science, Nagoya, Japan.
  • Nishimura Y; Department of Radiation Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
  • Yaegashi N; Department of Obstetrics and Gynecology, Tohoku University Graduate School of Medicine, Sendai, Japan.
  • Toita T; Radiation Therapy Center, Okinawa Chubu Hospital, Okinawa, Japan.
Jpn J Clin Oncol ; 49(9): 881-885, 2019 Sep 01.
Article en En | MEDLINE | ID: mdl-31613355
ABSTRACT
A single-arm multi-center confirmatory trial was started in Japan to confirm the efficacy and safety of post-radical hysterectomy concurrent chemoradiotherapy using intensity-modulated radiation therapy (IMRT-CCRT) for patients with high-risk uterine cervical cancer, for which the current standard treatment is CCRT using three-dimensional conformal radiation therapy (3DCRT-CCRT). This study began in April 2017 and a total of 220 patients will be accrued from 44 institutions within 3.5 years. The primary endpoint is 3-year relapse-free survival. The secondary endpoints are overall survival, loco-regional relapse-free survival, proportion of late lower gastrointestinal adverse events greater than or equal to grade 3, proportion of lower edema limbs, adverse events, and serious adverse events. This trial was registered at the Japan Registry of Clinical Trials as jRCTs031180194 (https//jrct.niph.go.jp/).
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias del Cuello Uterino / Radioterapia de Intensidad Modulada / Quimioradioterapia Tipo de estudio: Clinical_trials / Etiology_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Middle aged País/Región como asunto: Asia Idioma: En Revista: Jpn J Clin Oncol Año: 2019 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias del Cuello Uterino / Radioterapia de Intensidad Modulada / Quimioradioterapia Tipo de estudio: Clinical_trials / Etiology_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Middle aged País/Región como asunto: Asia Idioma: En Revista: Jpn J Clin Oncol Año: 2019 Tipo del documento: Article País de afiliación: Japón