中华内科杂志
中華內科雜誌
중화내과잡지
CHINESE JOURNAL OF INTERNAL MEDICINE
2014年
2期
99-103
,共5页
赵珺%任汉云%邱志祥%王茫桔%刘微%许蔚林%李渊%孙玉华%王莉红
趙珺%任漢雲%邱誌祥%王茫桔%劉微%許蔚林%李淵%孫玉華%王莉紅
조군%임한운%구지상%왕망길%류미%허위림%리연%손옥화%왕리홍
造血干细胞移植,异基因%肝功能异常%肝脏合并症%总生存%移植相关死亡
造血榦細胞移植,異基因%肝功能異常%肝髒閤併癥%總生存%移植相關死亡
조혈간세포이식,이기인%간공능이상%간장합병증%총생존%이식상관사망
Hematopoietic stem cell transplantation,allogeneic%Liver dysfunction%Hepatic complication%Overall survival%Transplant-related mortality
目的 探讨异基因造血干细胞移植(allo-HSCT)患者移植前和预处理期间肝功能异常的特征及其与肝脏合并症和预后的关系.方法 回顾性分析196例allo-HSCT治疗血液系统疾病患者,采集其移植前和预处理期间肝功能数据,观察其对造血重建、移植相关肝脏并发症、生存和移植相关死亡的影响.结果 196例患者中,38例移植前存在肝功能异常,159例预处理期间发生肝功能异常,28例(17.6%)出现3度肝损害,无4度肝损害出现.移植前和预处理期间肝功能异常对造血重建时间、肝静脉阻塞病(HVOD)、肝脏急性移植物抗宿主病(aGVHD)和慢性移植物抗宿主病(cGVHD)发生无显著影响.单因素分析显示年龄(P =0.022)、移植前疾病状态高危(P =0.003)、移植前AST(P=0.019)和TBil水平升高(P =0.015)、Ⅲ~Ⅳ度肝脏aGVHD(P=0.000)和HVOD(P=0.000)是影响总生存(OS)率的危险因素.多因素Cox回归分析显示移植前疾病状态为高危(P=0.002)、Ⅲ~Ⅳ度肝脏aGVHD(P=0.000)是影响OS率的独立危险因素,同时也是影响移植相关死亡(TRM)率的独立危险因素(P值分别为0.002和0.000),而移植前和预处理期间肝功能异常对OS率和TRM率无显著影响.结论 1~2度肝功能异常患者,在密切监测肝功能、充分保肝治疗及积极预防HVOD基础上,可考虑进行allo-HSCT.
目的 探討異基因造血榦細胞移植(allo-HSCT)患者移植前和預處理期間肝功能異常的特徵及其與肝髒閤併癥和預後的關繫.方法 迴顧性分析196例allo-HSCT治療血液繫統疾病患者,採集其移植前和預處理期間肝功能數據,觀察其對造血重建、移植相關肝髒併髮癥、生存和移植相關死亡的影響.結果 196例患者中,38例移植前存在肝功能異常,159例預處理期間髮生肝功能異常,28例(17.6%)齣現3度肝損害,無4度肝損害齣現.移植前和預處理期間肝功能異常對造血重建時間、肝靜脈阻塞病(HVOD)、肝髒急性移植物抗宿主病(aGVHD)和慢性移植物抗宿主病(cGVHD)髮生無顯著影響.單因素分析顯示年齡(P =0.022)、移植前疾病狀態高危(P =0.003)、移植前AST(P=0.019)和TBil水平升高(P =0.015)、Ⅲ~Ⅳ度肝髒aGVHD(P=0.000)和HVOD(P=0.000)是影響總生存(OS)率的危險因素.多因素Cox迴歸分析顯示移植前疾病狀態為高危(P=0.002)、Ⅲ~Ⅳ度肝髒aGVHD(P=0.000)是影響OS率的獨立危險因素,同時也是影響移植相關死亡(TRM)率的獨立危險因素(P值分彆為0.002和0.000),而移植前和預處理期間肝功能異常對OS率和TRM率無顯著影響.結論 1~2度肝功能異常患者,在密切鑑測肝功能、充分保肝治療及積極預防HVOD基礎上,可攷慮進行allo-HSCT.
목적 탐토이기인조혈간세포이식(allo-HSCT)환자이식전화예처리기간간공능이상적특정급기여간장합병증화예후적관계.방법 회고성분석196례allo-HSCT치료혈액계통질병환자,채집기이식전화예처리기간간공능수거,관찰기대조혈중건、이식상관간장병발증、생존화이식상관사망적영향.결과 196례환자중,38례이식전존재간공능이상,159례예처리기간발생간공능이상,28례(17.6%)출현3도간손해,무4도간손해출현.이식전화예처리기간간공능이상대조혈중건시간、간정맥조새병(HVOD)、간장급성이식물항숙주병(aGVHD)화만성이식물항숙주병(cGVHD)발생무현저영향.단인소분석현시년령(P =0.022)、이식전질병상태고위(P =0.003)、이식전AST(P=0.019)화TBil수평승고(P =0.015)、Ⅲ~Ⅳ도간장aGVHD(P=0.000)화HVOD(P=0.000)시영향총생존(OS)솔적위험인소.다인소Cox회귀분석현시이식전질병상태위고위(P=0.002)、Ⅲ~Ⅳ도간장aGVHD(P=0.000)시영향OS솔적독립위험인소,동시야시영향이식상관사망(TRM)솔적독립위험인소(P치분별위0.002화0.000),이이식전화예처리기간간공능이상대OS솔화TRM솔무현저영향.결론 1~2도간공능이상환자,재밀절감측간공능、충분보간치료급적겁예방HVOD기출상,가고필진행allo-HSCT.
Objective To investigate the characteristics of liver dysfunction pre-transplant and during conditioning period and its impacts on transplantation related hepatic complication,overall survival (OS) and transplant-related mortality (TRM).Methods A total of 196 patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT) at Peking University First Hospital were analyzed retrospectively.Liver function test for each patient was examined pre-transplant and during the period of conditioning.The correlation of liver dysfunction with hepatic complications,OS and TRM rates were analyzed.Results Liver dysfunction before transplantation was found in 38 (19.8%,38/192) patients,while damage of liver function during conditioning was found in 159 (81.1%) patients,28 of whom developed grade 3 hepatic dysfunction.There was no life-threatening impairment of liver function.No matter pre-transplant or during conditioning,liver dysfunction did not suggest apparent influence on the engraftment of neutrophil or platelet or the incidence of hepatic complications including hepatic veno occlusive disease (HVOD),acute graft versus host disease (aGVHD) and chronic graft versus host disease (cGVHD).Univariate analysis revealed that factors affecting OS rate included age (P =0.022),high risk stage (P =0.003),AST and TBil elevation before transplantation (P =0.019 and 0.015 respectively),Ⅲ-Ⅳ hepatic aGVHD (P =0.000) and HVOD(P =0.000).Multivariate Cox regression analysis revealed that high risk stage (P =0.002) and Ⅲ-Ⅳ hepatic aGVHD (P =0.000) were independent prognostic risk factors affecting both OS rate and TRM rate,while liver dysfunction before transplantation or during conditioning period had no apparent influence on OS rate or TRM rate.Conclusion Allo-HSCT would be administrated for the patients with mild impairment of liver function grade 1 and 2.