Efficacy of aspirin for stage III colorectal cancer: A randomized double-blind placebo-controlled trial (JCOG1503C, EPISODE-III trial).

Authors

null

Atsuo Takashima

Division of Gastrointestinal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan

Atsuo Takashima , Kenichi Miyamoto , Yuya Sato , Natsuko Okita , Manabu Shiozawa , Shigeki Yamaguchi , Ryo Inada , Yusuke Nishizawa , Masayuki Ohue , Nobuhiro Takiguchi , Junki Mizusawa , Hiroshi Katayama , Kenichi Nakamura , Taro Shibata , Haruhiko Fukuda , Yasuhiro Shimada , Yukihide Kanemitsu , Tetsuya Hamaguchi

Organizations

Division of Gastrointestinal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan, Japan Clinical Oncology Group Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan, Department of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama, Japan, Gastroenterological Surgery, Saitama Medical University International Medical Center, Hidaka-Shi, Japan, Kochi Health Sciences Center, Kochi, Japan, Division of Gastroenterological Surgery, Saitama Cancer Center, Saitama, Japan, Department of Gastroenterological Surgery, Osaka International Cancer Institite, Osaka, Japan, Department of Gastroenterological Surgery, Chiba Cancer Center, Chiba, Japan, Clinical Oncology Division, Kochi Health Sciences Center, Kochi, Japan, Department of Colorectal Surgery, National Cancer Center Hospital, Tokyo, Japan, Department of Gastroenterological Oncology, Saitama Medical University International Medical Center, Saitama, Japan

Research Funding

Other Government Agency

Background: Adjuvant chemotherapy is the current standard treatment for stage III colorectal cancer after curative resection. However, the prognosis of stage III colorectal cancer is still poor even after curative resection and adjuvant chemotherapy. Recently, several observational studies suggested the anti-tumor effect of aspirin for advanced colorectal cancer. The main mechanism of the anti-tumor effect by aspirin may be to suppress cyclooxygenase activity in the arachidonic acid cascade and to inhibit the production of prostaglandins involved in tumor growth. So far, aspirin showed a prolongation of survival for colorectal cancer in several retrospective studies. However, in these studies, aspirin was given not to be evaluated the effect on prognosis of colorectal cancer in adjuvant setting but to prevent cardiovascular event. In addition, baseline patient characteristics were imbalanced between aspirin group and non-aspirin group and both dosage amount and dosing period of aspirin were different among patients. Methods: We planned a randomized double-blind placebo-controlled phase III trial commenced in Japan in March 2018 to confirm the superiority of aspirin in terms of disease-free survival (DFS) over placebo for stage III colorectal cancer patients after curative resection. Patients receive aspirin (100 mg/day) or placebo for 3 years with the standard adjuvant chemotherapy of mFOLFOX6, CAPOX or capecitabine until relapse or unacceptable toxicities. The primary endpoint is DFS and the secondary endpoints are overall survival, relapse-free survival, relative dose intensity, adverse events, and serious adverse events. We assumed the 3-year DFS of aspirin arm as 74% based on two previous trials conducted by JCOG and expected a 6% increase in the 3-year DFS with aspirin adding to standard adjuvant chemotherapy after curative surgery. A total of 880 patients will be accrued from 20 Japanese institutions within 3 years, and 47 patients were enrolled as of Jan 31, 2019. Both aspirin and placebo are provided by Bayer Yakuhin Ltd. This trial has been registered at Japan Registry of Clinical Trials as jRCTs031180009 (https://jrct.niph.go.jp/detail/589). Clinical trial information: jRCTs031180009.

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Abstract Details

Meeting

2019 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Gastrointestinal (Colorectal) Cancer

Track

Gastrointestinal Cancer—Colorectal and Anal

Sub Track

Colorectal Cancer–Local-Regional Disease

Clinical Trial Registration Number

jRCTs031180009

Citation

J Clin Oncol 37, 2019 (suppl; abstr TPS3623)

DOI

10.1200/JCO.2019.37.15_suppl.TPS3623

Abstract #

TPS3623

Poster Bd #

111a

Abstract Disclosures

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