Second-generation tyrosine kinase inhibitors combined with allogeneic hematopoietic stem cell transp

来源 :The 35th World Congress of the International Society of Hema | 被引量 : 0次 | 上传用户：JK0803luowei

【摘要】

：

【作者】

：

Yanqing Huang Xingchen Gao Yilian Yang Huihui Song Wen Bao Zhengping Yu Jun Wang Gang Zhao Linlin Wang Zhi Chen Jiahua Ding

【机构】

：

Department of Hematology,Zhong Da Hospital,Southeast University,Nanjing,China

【出处】

：

The 35th World Congress of the International Society of Hema

【发表日期】

：

2014年5期

下载到本地 , 更方便阅读

下载此文赞助VIP

声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架

论文部分内容阅读

Blast crisis (BC)is highly refractory to therapy and has a poor prognosis.To determine the efficacy of TKIs-Ⅱ com bined with allogeneic hematopoietic stem cell transplantation (allo-HSCT) in CML BC,we present four consecutive,recent cases of CML BC in which TKIs-Ⅱ were used before or after allo-HSCT.

其他文献

Mir-663 Impairs the Effects of Bone Marrow-Derived Mesenchymal Stem Cells on MRL/Lpr Mice

Objective Previously we have shown that miR-663 was increased in bone marrow derived mesenchymal stem cells (BMSCs) from SLE patients and involved in the functional deficiency of BMSCs through inhibit

会议

The effect of overexpression of Bmi1 or Gata2 on hematopoietic differentiation of hiPSC/hESC in vitr

Thalassemia is a group of hereditary hemolytic anemia,which has high incidence in south China,especially inGuangdong,Guangxi and other province.Hematopoietic stem cell transplantation is the most effe

会议

Possible Role Of G-Csf On Neutrophil Activation,Endothelial Dysfunction And Haemostatic Changes In C

The aim of this study to evaluate granulocyte colony stimulating factor (G-CSF) level in chronic renal failure patients,and to investigate its impact on neutrophil activation,endothelial dysfunction a

会议

“In Vitro” Scf Treatment Downregulates Fpn1 And Gdf15 Mrna Expression In Human Beta-Thalassemic Eryt

Background And Aims Progressive iron overload is the most important and fatal complication in beta-thalassemia.However,little is known about the relationship among ineffective erythropoiesis,the role

会议

Evaluation of the ARKRAY ADAMS A1c HA-8180T analyzer for diagnosis of thalassemia and hemoglobinopat

The Arkray Adams A1c HA-8180T analyzer is relatively new HPLC based hemoglobin (Hb) analyzer designated for both Hb A1c testing and Hb typing using reverse-phase cation exchange chromatography.We exam

会议

Follow up of Turkish and Syrian Thalassemic Patients in Gaziantep Region/Turkey-Struggling with pati

Introduction Thalassemias are a heterogeneous group of autosomal recessive disorders that are characterized by hypochromic microcytic anemia caused by disturbed synthesis of one or more hemoglobin cha

会议

Thalassemia intermedia caused by interaction of beta-globin EKLF binding site mutation with Hb E and

Although thalassemia intermedia patients have mild anemia and do not require regular blood transfusion,they may still suffer from a number of serious clinical complications.We have characterized the m

会议

Increased Incidence Of Trisomy 8 In Aplastic Anemia Patients Combined With Behcet'S

Background Behcets disease (BD) is a disease of unknown cause which is clinically characterized by recurrent oral and genital ulcers,uveitis,polyarthritis,gastrointestinal involvement,and vasculitis.T

会议

Immunosuppressive treatment combined with cord blood infusion for12 patients in severe aplastic anem

Aim We report a single-center experience in treating 12 patients with severe aplastic anemia (SAA) who received immunosuppressive treatment combined with unrelated cord blood infusion.Methods The medi

会议

IL-1 receptor accessory protein as a surface marker for leukemia stem cells is related to clinical p

Chronic myeloid leukemia (CML) is a clonal disease from hematopoietic stem cells.Surviving leukemia stem cells (LSCs) and progenitor cells are a potential source for CML relapse and progression.Recent

会议

Second-generation tyrosine kinase inhibitors combined with allogeneic hematopoietic stem cell transp

与本文相关的学术论文