Bork, U.* ; Grützmann, R.* ; Rahbari, N.N.* ; Schölch, S.* ; Distler, M.* ; Reissfelder, C.* ; Koch, M.* ; Weitz, J.*
    
    
        
Prognostic relevance of minimal residual disease in colorectal cancer.
    
    
        
    
    
        
        World J. Gastroenterol. 20, 10296-10304 (2014)
    
    
 	
    
	
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			Open Access Gold as soon as Publ. Version/Full Text is submitted to ZB.
		
     
    
      
      
	
	    Presence of occult minimal residual disease in patients with colorectal cancer (CRC) has a strong prognostic impact on survival. Minimal residual disease plays a major role in disease relapse and formation of metastases in CRC. Analysis of circulating tumor cells (CTC) in the blood is increasingly used in clinical practice for disease monitoring of CRC patients. In this review article the role of CTC, disseminated tumor cells (DTC) in the bone marrow and micrometastases and isolated tumor cells (ITC) in the lymph nodes will be discussed, including literature published until September 2013. Occult disease is a strong prognostic marker for patient survival in CRC and defined by the presence of CTC in the blood, DTC in the bone marrow and/or micrometastases and ITC in the lymph nodes. Minimal residual disease could be used in the future to identify patient groups at risk, who might benefit from individualized treatment options.
	
	
	    
	
       
      
	
	    
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        Publication type
        Article: Journal article
    
 
    
        Document type
        Scientific Article
    
 
    
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        Keywords
        Circulating Tumor Cells ; Colorectal Cancer ; Disseminated Tumor Cells ; Isolated Tumor Cells ; Micrometastases ; Minimal Residual Disease ; Occult Disease
    
 
    
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        english
    
 
    
        Publication Year
        2014
    
 
    
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        ISSN (print) / ISBN
        1007-9327
    
 
    
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        2219-2840
    
 
    
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	    Volume: 20,  
	    Issue: 30,  
	    Pages: 10296-10304 
	    Article Number: ,  
	    Supplement: ,  
	
    
 
    
        
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            WJG Press
        
 
        
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        Peer reviewed
    
 
    
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        Institute of Pancreatic Islet Research (IPI)
    
 
    
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        Erfassungsdatum
        2014-12-31