中华内科杂志
中華內科雜誌
중화내과잡지
CHINESE JOURNAL OF INTERNAL MEDICINE
2008年
4期
316-319
,共4页
陈瑶%许兰平%刘开彦%刘代红%韩伟%陈欢%张耀臣%陈育红%黄晓军
陳瑤%許蘭平%劉開彥%劉代紅%韓偉%陳歡%張耀臣%陳育紅%黃曉軍
진요%허란평%류개언%류대홍%한위%진환%장요신%진육홍%황효군
白血病%造血干细胞移植%肝炎表面抗原,乙型%移植物抗宿主病
白血病%造血榦細胞移植%肝炎錶麵抗原,乙型%移植物抗宿主病
백혈병%조혈간세포이식%간염표면항원,을형%이식물항숙주병
Leukemia%Hematopoietic stem cell transplantation%Hepatitis B surface antigens%Graft vs host disease
目的 探讨HBsAg阳性患者接受异基因造血干细胞移植(allo-HSCT)后的肝脏不良事件的发生及影响该类患者长期存在的危险因素.方法 回顾性分析本所2001年3月至2006年11月接受allo-HSCT治疗的26例HBsAg阳性患者的临床资料.造血干细胞来源:18例为HLA配型相合同胞,7例为HLA配型不合亲缘供者,1例为无关供者.所有患者移植前后均排除丙型肝炎病毒感染.2例移植前HBV DNA阳性,其余均表达阴性.结果 26例患者急性移植物抗宿主病(Agvhd)累积发生率为50.0%.在可评估的20例中,5例发生了慢性GVHD,累积发生率25.0%.移植后出现肝功能异常共有15例(57.7%).出现肝功能受损的病因主要为:乙型肝炎及肝脏GVHD.移植后乙型肝炎再燃5年累积发生率33.4%,发生中位时间为82(65~159)d.拉米夫定预防性应用13例,1例发生乙型肝炎事件;未给药组为11例,7例发生乙型肝炎事件,两者累积发生率差异有统计学意义(P=0.006);预防用药组未发生一例肝衰竭,未预防用药组发生4例肝衰竭.死亡原因:5例肝衰竭,3例肺部感染,2例移植后疾病复发.26例患者中共有10例死亡,5年生存率(OS)为59.0%.多因素分析最终确定与OS发生相关的危险因素为肝衰竭(P=0.000).结论 HBsAg阳性患者接受allo-HSCT治疗后常出现肝功能异常表现,其首要病因为乙型肝炎,所导致的肝衰竭严重影响患者预后.而对HBsAg阳性患者预防性应用拉米夫定能够有效预防移植后乙型肝炎的复燃.
目的 探討HBsAg暘性患者接受異基因造血榦細胞移植(allo-HSCT)後的肝髒不良事件的髮生及影響該類患者長期存在的危險因素.方法 迴顧性分析本所2001年3月至2006年11月接受allo-HSCT治療的26例HBsAg暘性患者的臨床資料.造血榦細胞來源:18例為HLA配型相閤同胞,7例為HLA配型不閤親緣供者,1例為無關供者.所有患者移植前後均排除丙型肝炎病毒感染.2例移植前HBV DNA暘性,其餘均錶達陰性.結果 26例患者急性移植物抗宿主病(Agvhd)纍積髮生率為50.0%.在可評估的20例中,5例髮生瞭慢性GVHD,纍積髮生率25.0%.移植後齣現肝功能異常共有15例(57.7%).齣現肝功能受損的病因主要為:乙型肝炎及肝髒GVHD.移植後乙型肝炎再燃5年纍積髮生率33.4%,髮生中位時間為82(65~159)d.拉米伕定預防性應用13例,1例髮生乙型肝炎事件;未給藥組為11例,7例髮生乙型肝炎事件,兩者纍積髮生率差異有統計學意義(P=0.006);預防用藥組未髮生一例肝衰竭,未預防用藥組髮生4例肝衰竭.死亡原因:5例肝衰竭,3例肺部感染,2例移植後疾病複髮.26例患者中共有10例死亡,5年生存率(OS)為59.0%.多因素分析最終確定與OS髮生相關的危險因素為肝衰竭(P=0.000).結論 HBsAg暘性患者接受allo-HSCT治療後常齣現肝功能異常錶現,其首要病因為乙型肝炎,所導緻的肝衰竭嚴重影響患者預後.而對HBsAg暘性患者預防性應用拉米伕定能夠有效預防移植後乙型肝炎的複燃.
목적 탐토HBsAg양성환자접수이기인조혈간세포이식(allo-HSCT)후적간장불량사건적발생급영향해류환자장기존재적위험인소.방법 회고성분석본소2001년3월지2006년11월접수allo-HSCT치료적26례HBsAg양성환자적림상자료.조혈간세포래원:18례위HLA배형상합동포,7례위HLA배형불합친연공자,1례위무관공자.소유환자이식전후균배제병형간염병독감염.2례이식전HBV DNA양성,기여균표체음성.결과 26례환자급성이식물항숙주병(Agvhd)루적발생솔위50.0%.재가평고적20례중,5례발생료만성GVHD,루적발생솔25.0%.이식후출현간공능이상공유15례(57.7%).출현간공능수손적병인주요위:을형간염급간장GVHD.이식후을형간염재연5년루적발생솔33.4%,발생중위시간위82(65~159)d.랍미부정예방성응용13례,1례발생을형간염사건;미급약조위11례,7례발생을형간염사건,량자루적발생솔차이유통계학의의(P=0.006);예방용약조미발생일례간쇠갈,미예방용약조발생4례간쇠갈.사망원인:5례간쇠갈,3례폐부감염,2례이식후질병복발.26례환자중공유10례사망,5년생존솔(OS)위59.0%.다인소분석최종학정여OS발생상관적위험인소위간쇠갈(P=0.000).결론 HBsAg양성환자접수allo-HSCT치료후상출현간공능이상표현,기수요병인위을형간염,소도치적간쇠갈엄중영향환자예후.이대HBsAg양성환자예방성응용랍미부정능구유효예방이식후을형간염적복연.
Objective To explore the incidence and risk factors of hepatic events and overall survival among HBsAg positive leukemia patients after allo-hematopoietic stem cell transplantation (allo-HSCT). Methods A retrospective clinical study was conducted at the bone marrow transplant unit in our hospital between March 2001 and November 2006. A total of 26 HBsAg positive leukemia patients were included in the study.18 patients received HLA-identical sibling allo-HSCT, 7 patients received HLA-mismatched related and 1 patient received HLA-identical unrelated. All the patients were free from hepatitis C infection before and after allo-HSCT. HBV serologic markers,including HBsAg、HBeAg、HBsAb、HBeAb and HBcAb were tested. 2 patients were positive for HBV-DNA before allo-HSCT. Results The cumulative incidence for acute graft vs host disease(aGVHD) grades Ⅰ-Ⅳ was 50.0%. The cumulative incidence for chronic GVHD was 25.0%. 15(57. 7%)of all the patients had abnormalities of liver function after allo-HSCT. The types of hepatic disease were reactivation of HBV and hepatic GVHD. The cumulative incidence in 5 years for hepatitis B reactivation was 33.4%, the median day of hepatitis B reactivation was 82th(65th-159th)day. The virologic and clinical outcomes were compared between two groups:one received lamivudine as prophylactic(group 1)and the other did not receive lamivudine(group 2). After transplantation,1 patient in group 1 and 7 patients in group 2 had hepatitis due to reactivation of HBV. The cumulative incidence for hepatitis B reactivation was statistically different between the two groups(P=0.006). None in group 1 but 4 in group 2 died of HBV-related hepatic failure. 10 of the 26 patients died after transplantation. The overall survival(OS) in 5 years was 59.0%. The causes of death included hepatic failure(5 cases), lung infection(3 cases) and relapse of leukemia(2 cases). By multivariate Cox analysis, development of hepatic failure was a significant predictor of mortality(P=0.000). Conclusion HBsAg positive leukemia patients often suffered from hepatic injury after allo-HSCT. The principal cause of hepatic damage was the reactivation of HBV. Hepatic failure caused by HBV was the principal reason of death. Prophylaxis with lamivudine in HBsAg positive leukemia recipients can reduce the reactivation of HBV.