Prognostic impact of tumor budding in stage II colon cancer: A prospective study (SACURA trial).

Authors

null

Hideki Ueno

National Defense Medical College, Department of Surgery, Saitama, Japan

Hideki Ueno , Megumi Ishiguro , Eiji Nakatani , Toshiaki Ishikawa , Hiroyuki Uetake , Kenta Murotani , Shigeyuki Matsui , Naohiro Tomita , Yasuhiro Shimada , Keiichi Takahashi , Kenjiro Kotake , Masahiko Watanabe , Hidetaka Mochizuki , Satoshi Teramukai , Kenichi Sugihara

Organizations

National Defense Medical College, Department of Surgery, Saitama, Japan, Tokyo Medical and Dental University, Department of Translational Oncology, Tokyo, Japan, Translational Research Informatics Center, Foundation for Biomedical Research and Innovation, Division of Medical Statistics, Kobe, Japan, Tokyo Medical and Dental University, Graduate School of Medicine and Dentistry, Department of Specialized Surgeries, Tokyo, Japan, Aichi Medical University, Aichi, Japan, Nagoya University, Department of Biostatistics, Aichi, Japan, Hyogo College of Medicine, Department of Surgery, Division of Lower GI Surgery, Hyogo, Japan, Kochi Health Sciences Center, Division of Clinical Oncology, Kochi, Japan, Tokyo Metropolitan Cancer and Infectious Disease Center Komagome Hospital, Department of Surgery, Tokyo, Japan, Tochigi Cancer Center, Department of Surgery, Tochigi, Japan, Kitasato University School of Medicine, Department of Surgery, Kanagawa, Japan, Kyoto Prefectural University of Medicine, Department of Biostatistics, Kyoto, Japan, Tokyo Medical and Dental University, Tokyo, Japan

Research Funding

Other Foundation

Background: Growing number of studies indicate tumor budding is a significant prognostic factor in colorectal cancer (van Wyk, et al. Cancer Treat Rev 2015), but this has been shown only in retrospective studies. We prospectively evaluated prognostic factors in stage II colon cancer to determine their prognostic value in a multi-institutional phase III study (SACURA trial, ASCO2016 abst#3617). Methods: A total of 991 patients with curatively resected stage II colon cancer (2006–2010; 136 institutions) were included in the study. Tumor budding was defined as an isolated cancer cell or a cluster composed of fewer than five cells in the invasive frontal region, and was graded based on its number within a microscopic field of a 20x objective lens (0.785 mm2) in the hotspot. Tumors with < 5, 5–9, and ≥10 budding foci were classified as grades G1, G2, and G3, respectively. All clinical and pathological data including the grade of budding were prospectively recorded and prognostic analyses were performed at 5 years after the completion of registration. Results: According to budding grading, 376, 331 and 284 tumors were classified as G1, G2, and G3, and 5-year relapse-free survival (RFS) rate was 90.9%, 85.1%, and 74.4%, respectively (P< 0.0001). Budding grade was significantly associated with the incidence of recurrence in the liver, lung, lymph node, and peritoneum (P< 0.0001–0.01). Among conventional factors, T stage and the serum CEA levels were associated with RFS, however, tumor grade, lymphatic and venous invasions, and the number of lymph node examined were not significant factors. Multivariate analysis for RFS showed budding, along with T stage, exerted an independent influence on prognostic outcome. Budding grade surpassed T stage and tumor grade in the ability to stratify patients by RFS (Harrell’s c-index, 0.63, 0.59, and 0.54, respectively). Conclusions: Our prospective study indicates that the grade of tumor budding is more informative for prognostic prediction than conventional prognostic factors in stage II colon cancer. The role of this prognostic factor should be highlighted in the adjuvant treatment setting, and conversely, some of prognostic factors adopted in clinical guidelines may need to be reconsidered. Clinical trial information: NCT00392899

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Abstract Details

Meeting

2017 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

NCT00392899

Citation

J Clin Oncol 35, 2017 (suppl; abstr 3609)

DOI

10.1200/JCO.2017.35.15_suppl.3609

Abstract #

3609

Poster Bd #

232

Abstract Disclosures

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