Clinical value of circulating endothelial cell levels in metastatic colorectal cancer patients treated with first-line chemotherapy and bevacizumab

被引:37
|
作者
Malka, D. [2 ]
Boige, V. [2 ,3 ]
Jacques, N. [1 ]
Vimond, N. [1 ]
Adenis, A. [4 ]
Boucher, E. [5 ]
Pierga, J. Y. [6 ]
Conroy, T. [7 ]
Chauffert, B. [8 ]
Francois, E. [9 ]
Guichard, P. [10 ]
Galais, M. P. [11 ]
Cvitkovic, F. [12 ]
Ducreux, M. [2 ]
Farace, F. [1 ,3 ]
机构
[1] Inst Gustave Roussy, Lab Translat Res, F-94805 Villejuif, France
[2] Inst Gustave Roussy, Dept Med Oncol, Gastrointestinal Oncol Unit, F-94805 Villejuif, France
[3] Univ Paris 11, INSERM, U981, Villejuif, France
[4] Ctr Oscar Lambret, Dept Gastrointestinal Oncol, F-59020 Lille, France
[5] Ctr Eugene Marquis, Dept Med Oncol, Rennes, France
[6] Inst Curie, Dept Med Oncol, Paris, France
[7] Ctr Alexis Vautrin, Dept Med Oncol, Vandoeuvre Les Nancy, France
[8] Ctr Georges Francois, Dept Med Oncol, Dijon, France
[9] Ctr Antoine Lacassagne, Dept Med Oncol, F-06054 Nice, France
[10] Polyclin 4 Pavillons, Dept Med Oncol, Lormont, France
[11] Ctr Francois Baclesse, Dept Med Oncol, F-14021 Caen, France
[12] Ctr Rene Huguenin, Dept Med Oncol, St Cloud, France
关键词
bevacizumab; biomarker; chemotherapy; circulating endothelial cells; metastatic colorectal cancer; prognosis; FLOW-CYTOMETRIC ASSAY; VASCULAR DISORDERS; PERIPHERAL-BLOOD; SURVIVAL; QUANTIFICATION; FLUOROURACIL; OXALIPLATIN; COMBINATION; LEUCOVORIN; CARCINOMAS;
D O I
10.1093/annonc/mdr365
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: We investigated whether circulating endothelial cells (CECs) predict clinical outcome of first-line chemotherapy and bevacizumab in metastatic colorectal cancer (mCRC) patients. Patients and methods: In a substudy of the randomized phase II FNCLCC ACCORD 13/0503 trial, CECs (CD45-CD31+CD146+ 7-amino-actinomycin- cells) were enumerated in 99 patients by four-color flow cytometry at baseline and after one cycle of treatment. We correlated CEC levels with objective response rate (ORR), 6-month progression-free survival (PFS) rate (primary end point of the trial), PFS, and overall survival (OS). Multivariate analyses of potential prognostic factors, including CEC counts and Kohne score, were carried out. Results: By multivariate analysis, high baseline CEC levels were the only independent prognostic factor for 6-month PFS rate (P < 0.01) and were independently associated with worse PFS (P = 0.02). High CEC levels after one cycle were the only independent prognostic factor for ORR (P = 0.03). High CEC levels at both time points independently predicted worse ORR (P = 0.025), 6-month PFS rate (P = 0.007), and PFS (P = 0.02). Kohne score was the only variable associated with OS. Conclusion: CEC levels at baseline and after one treatment cycle may independently predict ORR and PFS in mCRC patients starting first-line bevacizumab and chemotherapy.
引用
收藏
页码:919 / U5
页数:9
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