Literature DB >> 18669452

Usefulness of the serum carcinoembryonic antigen kinetic for chemotherapy monitoring in patients with unresectable metastasis of colorectal cancer.

Isabelle Iwanicki-Caron1, Frédéric Di Fiore, Isabelle Roque, Emilie Astruc, Monica Stetiu, Aude Duclos, David Tougeron, Sandrine Saillard, Sébastien Thureau, Jacques Benichou, Bernard Paillot, Jean Pierre Basuyau, Pierre Michel.   

Abstract

PURPOSE: The aim of the study was to evaluate the relationship between serum carcinoembryonic antigen (CEA) kinetic and response to chemotherapy in patients with unresectable metastasis of colorectal cancer. PATIENTS AND METHODS: The kinetic was calculated using the slope of an exponential-regressive curve connecting the semi-logarithmic values of CEA. Receiver operating characteristic (ROC) curves were drawn to select the CEA slope thresholds to define patients with progressive or responsive disease with the highest sensitivity, specificity, and diagnosis accuracy odds ratio (DOR). The correlation between the CEA slopes and progression-free survival (PFS) was evaluated by the Cox model and Kaplan-Meier methods.
RESULTS: A total of 122 patients were included. Progression defined by CEA slope greater than +0.05 resulted in sensitivity of 85.7%, specificity of 85.1%, and DOR of 34. The area under the ROC (AUROC) curve was 0.885 (95% CI, 0.815 to 0.936; P = .0001). Response defined by CEA slope less than -0.2 resulted in sensitivity of 74.7%, specificity of 82.5%, and DOR of 16. The AUROC curve was 0.847 (95% CI, 0.770 to 0.906; P = .0001). The difference between AUROC curves calculated with six or four CEA values was not significant. PFS was correlated with CEA slopes (hazard ratio, 4.6; 95% CI, 2.48 to 8.57). The median PFS was 10 months for patients with CEA slope values less than -0.2 months versus 6 months for patients with CEA slope values greater than -0.2 (P < .0001).
CONCLUSION: These results suggest that the CEA kinetic is an accurate, simple, and noninvasive method to identify the disease progression in patients with unresectable metastasis of colorectal cancer.

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Year:  2008        PMID: 18669452     DOI: 10.1200/JCO.2007.15.0904

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  29 in total

1.  Tumor markers CEA and CA 19-9 correlate with radiological imaging in metastatic colorectal cancer patients receiving first-line chemotherapy.

Authors:  M Michl; J Koch; R P Laubender; D P Modest; C Giessen; Ch Schulz; V Heinemann
Journal:  Tumour Biol       Date:  2014-07-15

2.  Carcinoembryonic antigen reduction after medical treatment in patients with metastatic colorectal cancer: a systematic review and meta-analysis.

Authors:  Giuseppe Antonio Colloca; Antonella Venturino; Domenico Guarneri
Journal:  Int J Colorectal Dis       Date:  2019-01-22       Impact factor: 2.571

3.  Bevacizumab plus FOLFIRI-3 in chemotherapy-refractory patients with metastatic colorectal cancer in the era of biotherapies.

Authors:  François Ghiringhelli; Julie Vincent; Boris Guiu; Bruno Chauffert; Sylvain Ladoire
Journal:  Invest New Drugs       Date:  2010-11-06       Impact factor: 3.850

Review 4.  Emerging molecular biomarkers--blood-based strategies to detect and monitor cancer.

Authors:  Samir M Hanash; Christina S Baik; Olli Kallioniemi
Journal:  Nat Rev Clin Oncol       Date:  2011-03       Impact factor: 66.675

5.  Novel anti-filamin-A antibody detects a secreted variant of filamin-A in plasma from patients with breast carcinoma and high-grade astrocytoma.

Authors:  Ozge Alper; William G Stetler-Stevenson; Lyndsay N Harris; Wolfgang W Leitner; Metin Ozdemirli; Dan Hartmann; Mark Raffeld; Mones Abu-Asab; Stephen Byers; Zhengping Zhuang; Edward H Oldfield; Yanhe Tong; Elke Bergmann-Leitner; Wayne E Criss; Koichi Nagasaki; Samuel C Mok; Daniel W Cramer; F Seyda Karaveli; Raphaela Goldbach-Mansky; Paul Leo; Kurt Stromberg; Robert J Weil
Journal:  Cancer Sci       Date:  2009-06-17       Impact factor: 6.716

6.  Over-expression of Metastasis-associated in Colon Cancer-1 (MACC1) Associates with Better Prognosis of Gastric Cancer Patients.

Authors:  Shao-Hua Ge; Xiao-Jiang Wu; Xiao-Hong Wang; Xiao-Fang Xing; Lian-Hai Zhang; Yu-Bing Zhu; Hong Du; Bin Dong; Ying Hu; Jia-Fu Ji
Journal:  Chin J Cancer Res       Date:  2011-06       Impact factor: 5.087

7.  CEA Response and Depth of Response (DpR) to Predict Clinical Outcomes of First-Line Cetuximab Treatment for Metastatic Colorectal Cancer.

Authors:  Yu Sunakawa; Akihito Tsuji; Tadamichi Denda; Yoshihiko Segawa; Yuji Negoro; Ken Shimada; Mitsugu Kochi; Masato Nakamura; Masahito Kotaka; Hiroaki Tanioka; Akinori Takagane; Satoshi Tani; Tatsuro Yamaguchi; Takanori Watanabe; Masahiro Takeuchi; Masashi Fujii; Wataru Ichikawa
Journal:  Target Oncol       Date:  2017-12       Impact factor: 4.493

8.  A case of class 3 MEK1 mutated metastatic colorectal cancer with a non-durable tumor marker response to MEK and ERK inhibitors.

Authors:  Chongkai Wang; Jaideep Sandhu; Marwan Fakih
Journal:  J Gastrointest Oncol       Date:  2019-12

9.  Detection of a new embryonic antigen (ESA-10) in the blood of patients with cancer: preliminary results in the United States.

Authors:  Peter H Wiernik; Dahlia Elkadi; Alvaro Luongo-Cespedes; Julio Battistoni; Silvina Rossi; Susana Caceres; Raul Platero; Norma Piriz; Alvaro Lamas
Journal:  Med Oncol       Date:  2010-01-27       Impact factor: 3.064

10.  Tumor marker evolution: comparison with imaging for assessment of response to chemotherapy in patients with colorectal liver metastases.

Authors:  Robbert J de Haas; Dennis A Wicherts; Eduardo Flores; Michel Ducreux; Francis Lévi; Bernard Paule; Daniel Azoulay; Denis Castaing; Antoinette Lemoine; René Adam
Journal:  Ann Surg Oncol       Date:  2010-01-06       Impact factor: 5.344

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