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首页> 外文期刊>Bone marrow transplantation >Mobilization of PBSC for allogeneic transplantation by the use of the G-CSF biosimilar XM02 in healthy donors
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Mobilization of PBSC for allogeneic transplantation by the use of the G-CSF biosimilar XM02 in healthy donors

机译:通过使用G-CSF生物仿制药XM02在健康供体中动员PBSC进行异体移植

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摘要

The human recombinant G-CSF filgrastim has been widely used for the mobilization of CD34 + stem cells of healthy donors (HD). In 2008, the G-CSF biosimilar XM02 (Ratiograstim, Tevagrastim and Biograstim) was approved by the European Medicines Agency (EMA) for the mobilization of PBSC. However, there is limited experience in the application of biosimilar G-CSF for the mobilization of PBSC especially in HD. Therefore, we investigated in two cohorts (n=22), the efficacy and safety of PBSC mobilization by either biosimilar G-CSF or reference G-CSF. We observed a similar yield of CD34 + stem cells as well as CD3 + T-cells and nucleated cells in both groups and a safe engraftment in all patients with similar reconstitution of hematopoiesis in all hosts. In summary, we found a comparable efficacy and safety of biosimilar G-CSF when compared with reference G-CSF.
机译:人重组G-CSF非格司亭已被广泛用于动员健康供体(HD)的CD34 +干细胞。在2008年,G-CSF生物仿制药XM02(雷诺格拉司汀,梯瓦格拉司汀和生物格拉司汀)被欧洲药品管理局(EMA)批准用于动员PBSC。然而,在将生物仿制药G-CSF用于动员PBSC(尤其是HD)中的经验有限。因此,我们在两个队列(n = 22)中研究了通过生物仿制药G-CSF或参考G-CSF进行PBSC动员的有效性和安全性。我们观察到两组中的CD34 +干细胞以及CD3 + T细胞和有核细胞的收率相似,并且在所有宿主中具有相似造血功能重建的所有患者中,均可以安全植入。总而言之,我们发现与参考G-CSF相比,生物仿制药G-CSF的疗效和安全性相当。

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