首页> 外文期刊>Bone marrow transplantation >Increased acute GvHD and higher transplant-related mortality in non-caucasians undergoing standard sibling allogeneic stem cell transplantation.
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Increased acute GvHD and higher transplant-related mortality in non-caucasians undergoing standard sibling allogeneic stem cell transplantation.

机译:非高加索人进行同级同种异体干细胞移植后,急性GvHD升高,移植相关死亡率更高。

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We conducted a retrospective study to compare outcome in Caucasians and non-Caucasians undergoing standard sibling allogeneic SCT. End points of the study were to compare graft-versus-host disease (GvHD) occurrence and transplant-related mortality (TRM). There were 251 patients, 43 non-Caucasian and 208 Caucasian. A higher proportion of non-Caucasian patients developed acute GvHD (aGvHD) grade 2 or greater as compared to the Caucasian group (48 vs 26%, respectively) P = 0.02. With a median follow-up of 27 months, 26% (11/43) of non-Caucasians and 14% (29/208) of Caucasian patients had died from TRM, which accounted for 55% of all deaths in the non-Caucasian group compared to 33% in Caucasians, P = 0.02. Overall survival 12 months post transplant was 64 vs 69% in the non-Caucasian and Caucasian groups, respectively (P = 0.43). Although there were higher numbers of CMV-positive patients in the non-Caucasian group, there were no deaths from CMV reactivation in this subgroup. We conclude that there is increased TRM and aGvHD following standard sibling allograft in the non-Caucasian population and this could be due to either differences in tumour biology or extrinsic factors such as socio-economic factors, nutritional status, post transplant care or presenting with late stage disease.
机译:我们进行了一项回顾性研究,以比较接受标准同级异基因SCT的高加索人和非高加索人的结局。该研究的目的是比较移植物抗宿主病(GvHD)的发生率和移植相关死亡率(TRM)。有251名患者,43名非高加索人和208名高加索人。与高加索人相比,非高加索人患急性GvHD(aGvHD)2级或更高的比例更高(分别为48%和26%),P = 0.02。中位随访期为27个月,非高加索人中有26%(11/43)和高加索人中有14%(29/208)因TRM死亡,占非高加索人所有死亡的55%与高加索人中的33%相比,P = 0.02。非高加索人和高加索人组移植后12个月的总生存期分别为64%和69%(P = 0.43)。尽管非高加索人群中CMV阳性患者的数量较高,但该亚组中没有因CMV激活而死亡。我们得出结论,非高加索人群同种异体同种异体移植后,TRM和aGvHD升高,这可能是由于肿瘤生物学差异或外在因素(例如社会经济因素,营养状况,移植后护理或出诊较晚)引起的分期疾病。

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