TY - JOUR
T1 - Single-arm confirmatory trial of postoperative concurrent chemoradiotherapy using intensity modulated radiation therapy for patients with high-risk uterine cervical cancer
T2 - Japan Clinical Oncology Group study (JCOG1402)
AU - Murakami, Naoya
AU - Isohashi, Fumiaki
AU - Hasumi, Yoko
AU - Kasamatsu, Takahiro
AU - Okamoto, Hiroyuki
AU - Nakamura, Kenichi
AU - Shibata, Taro
AU - Ito, Yoshinori
AU - Ishikura, Satoshi
AU - Nishimura, Yasumasa
AU - Yaegashi, Nobuo
AU - Toita, Takafumi
N1 - Funding Information:
This study is supported by National Cancer Center Research and Development Funds (26-A-4, 29-A-3).
Funding Information:
Hokkaido University Hospital, Sapporo Medical University, Iwate Medical University Hospital, Tohoku University Hospital, Faculty of Medicine, University of Tsukuba, Tochigi Cancer Center, Jichi Medical University, Ibaraki Prefectural Central Hospital, Gunma University Hospital, Gunma Prefectural Cancer Center, Saitama Cancer Center, Saitama Medical University International Medical Center, Chiba University, Graduate School of Medicine, Chiba Cancer Center, National Cancer Center Hospital, Nihon University Itabashi Hospital, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Keio University Hospital, Jikei University Hospital, Cancer Institute Hospital of Japanese Foundation for Cancer Research, The University of Tokyo Hospital, Juntendo University Hospital, NTT Medical Center Tokyo, Showa University School of Medicine, Tokai University School of Medicine, Kitasato University School of Medicine, Kanagawa Cancer Center, Shinshu University, Shizuoka Cancer Center, Aichi Cancer Center Hospital, Nagoya University School of Medicine, Kyoto University Hospital, University Hospital Kyoto Prefectural University of Medicine, Osaka University Graduate School of Medicine, Kindai University Faculty of Medicine, Osaka International Cancer Institute, Osaka Medical College, Osaka City General Hospital, Hyogo Cancer Center, Kobe City Medical Center General Hospital, Tottori University Hospital, Shikoku Cancer Center, National Hospital Organization Kure Medical Cancer and Chugoku Cancer Center, Ehime University Hospital, Kyushu Cancer Center, Kyushu University Hospital, Kagoshima University Hospital, Kagoshima City Hospital, Okinawa Chubu Hospital, and University of the Ryukyus Hospital.
Publisher Copyright:
© 2019 The Author(s).
PY - 2019/10/15
Y1 - 2019/10/15
N2 - 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/).
AB - 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/).
KW - clinical trials
KW - concurrent chemoradiotherapy
KW - intensity-modulated radiation therapy
KW - phase III
KW - radical hysterectomy
KW - uterine cervical cancer
UR - http://www.scopus.com/inward/record.url?scp=85070081901&partnerID=8YFLogxK
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U2 - 10.1093/jjco/hyz098
DO - 10.1093/jjco/hyz098
M3 - Article
C2 - 31613355
AN - SCOPUS:85070081901
VL - 49
SP - 881
EP - 885
JO - Japanese Journal of Clinical Oncology
JF - Japanese Journal of Clinical Oncology
SN - 0368-2811
IS - 9
ER -