Analysis of clinical characteristics and outcome of patients with very high risk primary immunoglobulin light-chain amyloidosis 
	    		
		   		
		   			
		   		
	    	
    	 
    	10.3760/cma.j.issn.0253-2727.2017.02.005
   		
        
        	
        		- VernacularTitle: 极高危原发性轻链型淀粉样变患者的临床特征和预后分析 
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Jun FENG
			        		
			        		;
		        		
		        		
		        		
			        		Xufei HUANG
			        		
			        		;
		        		
		        		
		        		
			        		Congli ZHANG
			        		
			        		;
		        		
		        		
		        		
			        		Kaini SHEN
			        		
			        		;
		        		
		        		
		        		
			        		Chunlan ZHANG
			        		
			        		;
		        		
		        		
		        		
			        		Jian SUN
			        		
			        		;
		        		
		        		
		        		
			        		Zhuang TIAN
			        		
			        		;
		        		
		        		
		        		
			        		Xinxin CAO
			        		
			        		;
		        		
		        		
		        		
			        		Lu ZHANG
			        		
			        		;
		        		
		        		
		        		
			        		Daobin ZHOU
			        		
			        		;
		        		
		        		
		        		
			        		Jian LI
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. Department of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		Primary light chain amyloidosis;
			        		
			        		
			        		
				        		Very high risk;
			        		
			        		
			        		
				        		Bortezomib
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Chinese Journal of Hematology
	            		
	            		 2017;38(2):107-111
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	 Objective:To evaluate the clinical characteristics and outcomes of very high risk patients with primary immunoglobulin light-chain amyloidosis (pAL) at a single center in China.
				        	
				        
				        	Method:Clinical data, treatment and outcome of 205 pAL patients in Peking Union Medical College Hospital from January 2009 to February 2016 were retrospectively analyzed. A 'very high risk’ group includes patients with Mayo 2004 stage Ⅲb and Mayo 2012 stage 4.
				        	
				        
				        	Results:Of 205 patients, 34 (16.6%) were defined as very high risk pAL patients. The median age at diagnosis was 57 (20-84) years, and 22 patients (64.7%) were male. All 34 patients were diagnosed with cardiac involvement, multi-organ involvement was observed in 15 patients (44.1%) , and 27 (81.8%) had New York Heart Association Class Ⅲ or Ⅳ. Median values of serum cTnI, NT-proBNP, and free light chains difference were 0.25 μg/L, 11 733 ng/L, and 403 mg/L, respectively. Eight (24.2%) had more than 10% plasma cell on the bone marrow aspirate. Sixteen (47.1%) patients received bortezomib based chemotherapy and overall hematologic response rate was 58.3%. Median overall survival (OS) was 4 months. The estimated OS at 3, 6, 12, and 24 months was 51.3%, 44.0%, 35.2%, and 29.6%, respectively. Fourteen (41.2%) patients died within 3 months after the diagnosis. The estimated 1-year survival rate for the patients who got hematologic response, without hematologic response, and palliative treatment was 90.9%, 11.1%, and 0, respectively (P<0.001) .
				        	
				        
				        	Conclusion:Patients with very high risk pAL had very poor prognosis and the early death rate remained high. Those patients who obtained hematologic remission would have significantly better outcomes.