CEA response at four weeks as an early predictor for outcomes in patients (pts) with metastatic colorectal cancer (mCRC) treated with first-line cetuximab-based chemotherapy: A STEP-analysis in the JACCRO CC-05/06 trials.

Authors

Yu Sunakawa

Yu Sunakawa

Department of Clinical Oncology, St. Marianna University School of Medicine, Kawasaki, Japan

Yu Sunakawa , Xuemin Fang , Masahito Kotaka , Hiroaki Tanioka , Akinori Takagane , Satoshi Tani , Tatsuro Yamaguchi , Takanori Watanabe , Toshiki Masuishi , Masahiro Tsuda , Tatsuya Okuno , Takao Tamura , Kaoru Furushima , Hidekazu Kuramochi , Junichi Koike , Yutaka Yonemura , Hisateru Yasui , Masahiro Takeuchi , Masashi Fujii , Wataru Ichikawa

Organizations

Department of Clinical Oncology, St. Marianna University School of Medicine, Kawasaki, Japan, Department of Clinical Medicine (Biostatistics), School of Pharmacy, Kitasato University, Tokyo, Japan, Gastrointestinal Cancer Center, Sano Hospital, Kobe, Japan, Department of Clinical Oncology, Kawasaki Medical School Hospital, Kurashiki, Japan, Department of Surgery, Hakodate Goryoukaku Hospital, Hakodate, Japan, Department of Medical Oncology, Kohnan Hospital, Kobe, Japan, Department of Surgery, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Tokyo, Japan, Department of Surgery, Himeji Red Cross Hospital, Himeji, Japan, Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan, Department of Gastroenterology, Hyogo Cancer Center, Akashi, Japan, Division of Gastroenterology, Department of Internal Medicine, Graduate School of Medicine, Kobe University, Kobe, Japan, Department of Medical Oncology, Kindai University Nara Hospital, Ikoma, Japan, Department of Surgery, NTT Medical Center, Tokyo, Japan, Department of Chemotherapy, Tokyo Woman's Medical University, Yachiyo Medical Center, Yachiyo, Japan, Gastroenterological Surgery, Omori Medical Center, Toho University School of Medicine, Tokyo, Japan, Department of Surgery, Kishiwada Tokushukai Hospital, Kishiwada, Japan, Department of Medical Oncology, Kobe City Medical Center General Hospital, Kobe, Japan, Department of Digestive Surgery, Nihon University School of Medicine, Tokyo, Japan, Division of Medical Oncology, Showa University Fujigaoka Hospital, Yokohama, Japan

Research Funding

Other

Background: We have reported that carcinoembryonic antigen (CEA) response correlated with clinical outcomes of 1st-line cet-based therapy (Target Oncol 2017). Early tumor shrinkage (ETS) is considered to be an on-treatment biomarker for outcomes of chemotherapy; however, clinical biomarkers to predict outcomes earlier are warranted. Methods: This study included 69 pts who were assessable for CEA at baseline and 4 wks, and with observed survival time from 2 phase II trials of 1st-line therapy for KRAS exon2 wild-type mCRC; JACCRO CC-05 of cet plus FOLFOX (UMIN000004197) and CC-06 of cet plus SOX (UMIN000007022). We investigated the influence of baseline age, gender, PS, primary tumor sidedness (PTS), number of tumor sites, as well as the CEA decrease at 4 wks to the patient’s OS and PFS. Results: PTS and the CEA decrease at 4 wks were found to be important predictors to OS and PFS. Baseline CEA and CEA decrease at 4 wks were median of 31.0 (range, 1.0-20920.0) and median of 35% (range, -259%-97%), respectively. The STEP-analysis indicated that CEA response was most significantly associated with OS when a cut-off value of 50% for CEA-responder (HR 0.49, log-rank test p = 0.03). Median OS in responders (n = 25) and non-responders (n = 44) were 36.2 m and 21.5 m, respectively. When the same cut-off value was used, median PFS in responders and non-responders were 11.6 m and 6.5 m, respectively (HR 0.64, log-rank test p = 0.08). In addition, a multivariate Cox Proportional-Hazards Model with both PTS and CEA response as risk factors showed that PTS correlated with both OS and PFS. In pts with left-sided tumors, non-responders (n = 33) had shorter OS and PFS compared to responders (n = 23). In the above 2-covariate Cox proportional hazard model, adjusted HR for CEA 50% decrease is 0.55, p = 0.1; adjusted HR for PTS is 2.66, p = 0.008. Conclusions: Our analysis suggests 50% CEA decrease at 4 wks as an early on-treatment biomarker for 1st-line cet-based therapy in mCRC. It may potentially predict outcomes earlier compared to ETS. Also, CEA response at 4 wks may differentiate pts who receive more benefit from cet treatment in left-sided tumors. Clinical trial information: UMIN000004197 and UMIN000007022.

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Abstract Details

Meeting

2019 Gastrointestinal Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session C: Cancers of the Colon, Rectum, and Anus

Track

Cancers of the Colon, Rectum, and Anus

Sub Track

Translational Research

Clinical Trial Registration Number

UMIN000004197 and UMIN000007022

Citation

J Clin Oncol 37, 2019 (suppl 4; abstr 543)

DOI

10.1200/JCO.2019.37.4_suppl.543

Abstract #

543

Poster Bd #

F6

Abstract Disclosures