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A randomized phase II study comparing preoperative mFOLFOX6 versus FOLFOXIRI for locally advanced colon cancer: JCOG2006.
Hashimoto, Tadayoshi; Maruyama, Satoshi; Takii, Yasumasa; Mizusawa, Junki; Kataoka, Tomoko; Fukuda, Haruhiko; Tsukamoto, Shunsuke; Takashima, Atsuo; Hamaguchi, Tetsuya; Kanemitsu, Yukihide.
Afiliação
  • Hashimoto T; Japan Clinical Oncology Group Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.
  • Maruyama S; Department of Surgery, Niigata Cancer Center Hospital, Niigata, Japan.
  • Takii Y; Department of Surgery, Niigata Cancer Center Hospital, Niigata, Japan.
  • Mizusawa J; Japan Clinical Oncology Group Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.
  • Kataoka T; Japan Clinical Oncology Group Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.
  • Fukuda H; Japan Clinical Oncology Group Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan.
  • Tsukamoto S; Department of Colorectal Surgery, National Cancer Center Hospital, Tokyo, Japan.
  • Takashima A; Department of Gastrointestinal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Hamaguchi T; Department of Gastroenterological Oncology, Saitama Medical University International Medical Center, Hidaka, Japan.
  • Kanemitsu Y; Department of Colorectal Surgery, National Cancer Center Hospital, Tokyo, Japan.
Future Oncol ; 19(28): 1897-1904, 2023 Sep.
Article em En | MEDLINE | ID: mdl-37750332
ABSTRACT
The prognosis of locally advanced colon cancer (LACC) with surgical resection followed only by adjuvant chemotherapy is poor. Preoperative chemotherapy for LACC patients with risk factors such as cT4bN+ or cT3-4aN2-3 has attracted attention. Here, the authors describe the rationale and design of JCOG2006, a randomized phase II study comparing preoperative chemotherapy with mFOLFOX6 versus FOLFOXIRI for LACC. Their efficacy and safety are evaluated and a determination of which is the more promising treatment will be conducted in a subsequent phase III trial. A total of 86 patients will be accrued from 44 institutions over 2 years. The primary end point is the proportion of patients with a Tumor Regression Score of 0-2, and secondary end points include overall survival, response rate and adverse events. Clinical Trial Registration jRCTs031210365 (https//jrct.niph.go.jp/).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias do Colo Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias do Colo Idioma: En Ano de publicação: 2023 Tipo de documento: Article