医学
累积发病率
入射(几何)
造血干细胞移植
移植
移植物抗宿主病
间充质干细胞
内科学
干细胞
造血
胃肠病学
免疫学
外科
肿瘤科
病理
物理
光学
生物
遗传学
作者
Li Ding,Dongmei Han,Hong-Min Yan,Jie-Xin Zhou,Xiao-Li Zheng,Ling Zhu,Mei Xue,Jing Liu,Ning Mao,Zi‐Kuan Guo,Hongmei Ning,Heng-Xiang Wang,Heng Zhu
标识
DOI:10.1038/s41409-022-01688-5
摘要
Although haploidentical stem cell transplantation (haplo-HSCT) offers almost all acute lymphoblastic leukaemia (ALL) patients an opportunity for immediate transplantation, it exhibits a higher incidence of graft failure and graft versus host disease (GVHD). Mesenchymal stem cells (MSCs) are characterised by their haematopoiesis-promoting and immunomodulatory capacity. Thus, we designed a combination of haplo-HSCT and MSCs for ALL patients. ALL patients (n = 110) were given haploidentical HSCs combined with allogenic MSCs, and ALL patients without MSC infusion (n = 56) were included as controls. The 100-day cumulative incidences of grade ≥2 acute GVHD (aGVHD) and grade ≥3 aGVHD were 40.00% and 9.09% compared to 42.32% (P = 0.79) and 22.79% (P = 0.03) in patients without MSC infusion, respectively. The 3-year cumulative incidences of chronic GVHD (cGVHD) and extensive cGVHD were 22.27% and 10.27% compared to 32.14% (P = 0.19) and 22.21% (P = 0.04) in patients without MSC infusion, respectively. No significant differences in the 3-year relapse incidence, nonrelapse mortality, leukaemia-free survival or overall survival in groups with and without MSC cotransplantation were observed. Multivariate analysis showed that MSC infusion contributed to a lower risk of developing extensive cGVHD. Our data suggested that haplo-HSCT combined with MSCs may provide an effective and safe treatment for ALL patients.
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