Circulating tumor cells criteria (CyCAR) versus standard RECIST criteria for treatment response assessment in metastatic colorectal cancer patients

被引:23
作者
Delgado-Urena, Mayte [1 ]
Ortega, Francisco G. [2 ]
de Miguel-Perez, Diego [2 ,3 ]
Rodriguez-Martinez, Alba [1 ,2 ,3 ,4 ,5 ]
Garcia-Puche, Jose L. [1 ,2 ]
Ilyine, Hugh [4 ]
Lorente, Jose A. [2 ,3 ]
Exposito-Hernandez, Jose [1 ]
Carmen Garrido-Nayas, M. [2 ]
Delgado-Ramirez, Miguel [5 ]
Jose Serrano, M. [1 ,2 ]
机构
[1] Clin Univ Hosp, Integral Oncol Div, Av Dr Oloriz 16, Granada 18012, Spain
[2] Univ Granada, Andalusian Reg Govt PTS, Liquid Biopsy & Metastasis Res Grp, GENYO,Ctr Genom & Oncol Res,Pfizer, Ave Ilustrac 114, Granada 18016, Spain
[3] Univ Granada, Fac Med, Legal Med & Toxicol Dept, Lab Genet Identificat, Ave Invest 11, E-18071 Granada, Spain
[4] DestiNA Genom Ltd, 7-11 Melville St, Edinburgh EH3 7PE, Midlothian, Scotland
[5] Univ Jaen, CIBERESP, Div Prevent Med & Publ Hlth, Campus Lagunillas, Jaen 23072, Spain
关键词
Metastatic colorectal cancer; Bevacizumab; Circulating tumor cells; RECIST; CyCAR; Prognosis; ENDOTHELIAL GROWTH-FACTOR; BREAST-CANCER; PROGRESSION; EXPRESSION; SURVIVAL; CHEMOTHERAPY; BEVACIZUMAB; INHIBITION; STRATEGIES; MARKER;
D O I
10.1186/s12967-018-1624-2
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: The use of circulating tumor cells (CTCs) as indicators of treatment response in metastatic colorectal cancer (mCRC) needs to be clarified. The objective of this study is to compare the Response Evaluation Criteria in Solid Tumors (RECIST) with the Cytologic Criteria Assessing Response (CyCAR), based on the presence and phenotypic characterization of CTCs, as indicators of FOLFOX-bevacizumab treatment response. Methods: 77 mCRC blood samples from FOLFOX-bevacizumab treated patients were analyzed to isolate CTCs before and after (12 and 24 weeks) treatment, using an immunomagnetic separation method. VEGFR expression was identified by double immunostaining. Results: We observed a decrease of CTCs (42.8 vs. 18.2%) and VEGFR positivity (69.7% vs. 41.7%) after treatment. According to RECIST, 6.45% of the patients did not show any clinical benefit, whereas 93.55% patients showed a favorable response at 12 weeks. According to CyCAR, 29% had a non-favorable response and 71% patients did not. No significant differences were found between the response assessment by RECIST and CyCAR at 12 or 24 weeks. However, in the multivariate analysis, RECIST at 12 weeks and CyCAR at 24 weeks were independent prognostic factors for OS (HR: 0.1, 95% CI 0.02-0.58 and HR: 0.35, 95% CI 0.12-0.99 respectively). Conclusions: CyCAR results were comparable to RECIST in evaluating the response in mCRC and can be used as an alternative when the limitation of RECIST requires additional response analysis techniques.
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页数:11
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