- VernacularTitle:骨髓增生异常综合征患者合并疾病的预后意义研究
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			        		Yi LI
			        		
			        		
			        		
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			        		Tiejun QIN
			        		
			        		
			        		
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			        		Zefeng XU
			        		
			        		
			        		
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			        		Yue ZHANG
			        		
			        		
			        		
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			        		Liwei FANG
			        		
			        		
			        		
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			        		Hongli ZHANG
			        		
			        		
			        		
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			        		Lijuan PAN
			        		
			        		
			        		
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			        		Naibo HU
			        		
			        		
			        		
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			        		Shiqiang QU
			        		
			        		
			        		
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			        		Bing LI
			        		
			        		
			        		
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			        		Zhijian XIAO
			        		
			        		
			        		
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			        		Author Information
			        		
 - Publication Type:Journal Article
 - MeSH: Abnormal Karyotype; Blood Platelets; Comorbidity; Humans; Leukocytes; Myelodysplastic Syndromes; Prognosis; Retrospective Studies; Risk
 - From: Chinese Journal of Hematology 2015;36(3):196-201
 - CountryChina
 - Language:Chinese
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		        	Abstract:
			       	
			       		
				        
				        	
OBJECTIVETo discuss the impact of comorbidities on the outcomes of patients with MDS.
METHODSThe clinical characteristics of 676 MDS patients with detailed comorbidities evaluations was analyzed retrospectively.
RESULTSThere were 395/676 cases (58.4%) with comorbidities (group 1), 281/676 cases (41.6%) without (group 2). Significant differences were seen in the distribution of age (≥ 60 y), bone marrow blasts, abnormal karyotype, WHO 2008 subtypes and IPSS-R risk cohorts (P<0.05) between the two groups. While gender, HGB concentrations, WBC levels, platelet levels and serum ferritin were not significantly different (P>0.05). Independent prognostic significance of comorbidities was seen in both uni-variate and multi-variate analyses (P<0.001). According to MDS-specific comorbidity index (MDS-CI), the median survival were 32(1-153) months, 19(2-85) months and 13(1-37) months in the low-risk, intermediate-risk and high-risk cohorts respectively, while 96(1-166) months in cohorts without any comorbidities, of which significant differences were seen (P<0.001). The MDS-CI allowed further stratification in the IPSS-R low-risk, intermediate-risk and high-risk cohorts (P<0.001).
CONCLUSIONComorbidities provides prognostic stratification independently of IPSS-R for MDS patients.
 
            
