Hepatectomy Followed by mFOLFOX6 Versus Hepatectomy Alone for Liver-Only Metastatic Colorectal Cancer (JCOG0603): A Phase II or III Randomized Controlled Trial.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
01 12 2021
Historique:
pubmed: 15 9 2021
medline: 29 12 2021
entrez: 14 9 2021
Statut: ppublish

Résumé

Adjuvant chemotherapy after hepatectomy is controversial in liver-only metastatic colorectal cancer (CRC). We conducted a randomized controlled trial to examine if adjuvant modified infusional fluorouracil, leucovorin, and oxaliplatin (mFOLFOX6) is superior to hepatectomy alone for liver-only metastasis from CRC. In this phase II or III trial (JCOG0603), patients age 20-75 years with confirmed CRC and an unlimited number of liver metastatic lesions were randomly assigned to hepatectomy alone or 12 courses of adjuvant mFOLFOX6 after hepatectomy. The primary end point of phase III was disease-free survival (DFS) in intention-to-treat analysis. Between March 2007 and January 2019, 300 patients were randomly assigned to hepatectomy alone (149 patients) or hepatectomy followed by chemotherapy (151 patients). At the third interim analysis of phase III with median follow-up of 53.6 months, the trial was terminated early according to the protocol because DFS was significantly longer in patients treated with hepatectomy followed by chemotherapy. With median follow-up of 59.2 months, the updated 5-year DFS was 38.7% (95% CI, 30.4 to 46.8) for hepatectomy alone compared with 49.8% (95% CI, 41.0 to 58.0) for chemotherapy (hazard ratio, 0.67; 95% CI, 0.50 to 0.92; one-sided DFS did not correlate with OS for liver-only metastatic CRC. Adjuvant chemotherapy with mFOLFOX6 improves DFS among patients treated with hepatectomy for CRC liver metastasis. It remains unclear whether chemotherapy improves OS.

Identifiants

pubmed: 34520230
doi: 10.1200/JCO.21.01032
doi:

Substances chimiques

Organoplatinum Compounds 0

Banques de données

UMIN-CTR
['UMIN000000653']

Types de publication

Clinical Trial, Phase II Clinical Trial, Phase III Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3789-3799

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Auteurs

Yukihide Kanemitsu (Y)

National Cancer Center Hospital, Tokyo, Japan.

Yasuhiro Shimizu (Y)

Aichi Cancer Center Hospital, Nagoya, Japan.

Junki Mizusawa (J)

National Cancer Center Hospital, Tokyo, Japan.

Yoshitaka Inaba (Y)

Aichi Cancer Center Hospital, Nagoya, Japan.

Tetsuya Hamaguchi (T)

Saitama Medical University International Medical Center, Hidaka, Japan.

Dai Shida (D)

National Cancer Center Hospital, Tokyo, Japan.

Masayuki Ohue (M)

Osaka International Cancer Institute, Osaka, Japan.

Koji Komori (K)

Aichi Cancer Center Hospital, Nagoya, Japan.

Akio Shiomi (A)

Shizuoka Cancer Center Hospital, Shizuoka, Japan.

Manabu Shiozawa (M)

Kanagawa Cancer Center, Kanagawa, Japan.

Jun Watanabe (J)

Yokohama City University Medical Center, Yokohama, Japan.

Takeshi Suto (T)

Yamagata Prefectural Central Hospital, Yamagata, Japan.

Yusuke Kinugasa (Y)

Tokyo Medical and Dental University, Tokyo, Japan.

Yasumasa Takii (Y)

Niigata Cancer Center Hospital, Niigata, Japan.

Hiroyuki Bando (H)

Ishikawa Prefectural Central Hospital, Kanazawa, Japan.

Takaya Kobatake (T)

National Hospital Organization Shikoku Cancer Center, Matsuyama, Japan.

Masafumi Inomata (M)

Oita University Faculty of Medicine, Yufu, Japan.

Yasuhiro Shimada (Y)

Kochi Health Sciences Center, Kochi, Japan.

Hiroshi Katayama (H)

National Cancer Center Hospital, Tokyo, Japan.

Haruhiko Fukuda (H)

National Cancer Center Hospital, Tokyo, Japan.

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Classifications MeSH