CD133 status influences in prognosis of patients with metastatic colorectal cancer receiving cetuximab.

Authors

null

Dai Inoue

Department of Medical Oncology, Cancer Institute Hospital, Tokyo, Japan

Dai Inoue , Satoshi Matsusaka , Noriko Yamamoto , Mitsukuni Suenaga , Yuji Mishima , Eiji Shinozaki , Yasuhito Terui , Nobuyuki Mizunuma , Yuichi Ishikawa , Kiyohiko Hatake

Organizations

Department of Medical Oncology, Cancer Institute Hospital, Tokyo, Japan, Department of Medical Oncology of Cancer Institute Hospital, Clinical Chemotherapy, Cancer Chemotherapy Center of Japanese Foundation for Cancer Research, Tokyo, Japan, Department of Pathology, Cancer Institute Hospital, Tokyo, Japan, Clinical Chemotherapy, Cancer Chemotherapy Center of Japanese Foundation for Cancer Research, Tokyo, Japan, Division of Pathology, Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan

Research Funding

No funding sources reported

Background: Recently, the cancer stem cell (CSC) theory has been proposed, and CD133 has been suggested as a potential marker of CSCs in metastatic colorectal cancer (mCRC). Cetuximab, an IgG1 anti-EGFR chimeric mouse/human monoclonal antibody, has been approved for the treatment of mCRC. The purpose of this study is to evaluate the prognostic significance of CD133 expression in mCRC treated with cetuximab in combination with chemotherapy. Methods: We evaluated the prognosis of pts with mCRC treated with cetuximab retrospectively, and performed immunohistochemical staining to analyze the CD133 status. Non-parametric statistics, univariate and multivariate analysis were used. Results: From October 2008 to June 2009, 56 pts with measurable metastatic colorectal cancer were received cetuximab and 43 were evaluable. Patients characteristics were as follows : median age : 59.6 years (range 28-80) , PS 0/1 : 30/13 , colon/rectum : 28/15 , metastatic site (liver +/- : 35/8 , lung +/- : 32/11 , bone +/- : 6/37 , peritoneum +/- : 6/37 , lymph node +/- : 11/32 , local +/- : 3/40), best response rate was 9.3% (CR/PR/SD/PD : 1/3/19/11). Compared with CD133- pts with colorectal cancer , the progression-free survival (PFS) of CD133+ pts was significantly better (5.5 month; 95% CI, 4.4-6.7,p=0.026), and median overall survival (OS) was also significantly better (11.0 month; 95% CI, 5.4-16.5, p=0.002). In univariate analysis, liver metastasis, lung metastasis, peritoneal metastasis, lymph node metastasis, age, and CD133 at the baseline predicted PFS, and age, gender, liver metastasis, lung metastasis, bone metastasis, peritoneal metastasis, lymph node metastasis at the baseline, the presence of skin rash, and CD133 predicted OS. In order to evaluate the independent predictive effect of chemotherapy, multivariate Cox regression analysis was carried out. It showed that CD133 was the strongest predictor. Conclusions: CD133 status at the baseline was correlated with the prognosis of patients treated with cetuximab, suggesting that CD133 status might play a role to estimate the prognosis.

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Abstract Details

Meeting

2012 Gastrointestinal Cancers Symposium

Session Type

Poster Session

Session Title

General Poster Session C: Cancers of the Colon and Rectum

Track

Cancers of the Colon, Rectum, and Anus

Sub Track

Translational Research

Citation

J Clin Oncol 30, 2012 (suppl 4; abstr 509)

DOI

10.1200/jco.2012.30.4_suppl.509

Abstract #

509

Poster Bd #

C32

Abstract Disclosures

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