首页> 外文期刊>Bone marrow transplantation >Successive double high-dose chemotherapy with peripheral blood stem cell rescue collected during a single leukapheresis round in patients with high-risk pediatric solid tumors: a pilot study in a single center.
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Successive double high-dose chemotherapy with peripheral blood stem cell rescue collected during a single leukapheresis round in patients with high-risk pediatric solid tumors: a pilot study in a single center.

机译:高危儿科实体瘤患者在单次白细胞分离期间收集了连续两次大剂量化疗,并进行了外周血干细胞抢救:在单个中心进行的一项初步研究。

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In total, 18 of 26 double high-dose chemotherapies (HDCT) in pediatric solid tumors were rescued with peripheral blood stem cells collected during a single leukapheresis round (single-harvest group, SHG). In the remaining eight HDCT, additional leukapheresis were necessary after the first HDCT (HDCT1) to rescue the second HDCT (HDCT2) (double-harvest group, DHG). Stem cell collection after HDCT1 was inefficient and delayed in patients who had received prior chemotherapy before HDCT1. The interval between HDCT1 and HDCT2 was shorter in SHG than in DHG (median 62.5 days vs 178.5 days, P-value=0.002). Hematologic recovery in HDCT2 was delayed compared to HDCT1. However, there was no difference in hematologic recovery between SHG and DHG. A high rate of treatment-related mortality (TRM) was recorded during HDCT2, but there was no evidence that the shorter interval caused a higher rate of TRM (P-value=0.454). The probability of disease-free survival at 2 years after HDCT2 in the SHG and DHG were 66.7 and 25.0%, respectively (P-value=0.031). Therefore, to administer the second HDCT earlier in double HDCT, and thus to improve the survival of patients with high-risk solid tumors, the single-harvest approach is recommended rather than the double-harvest approach.Bone Marrow Transplantation (2003) 31, 447-452. doi:10.1038/sj.bmt.1703869
机译:总共有26例小儿实体瘤双重高剂量化学疗法(HDCT)中的18例通过单次白细胞分离术(单采血组,SHG)收集的外周血干细胞进行了抢救。在其余的八个HDCT中,在第一个HDCT(HDCT1)之后需要进行额外的白细胞穿刺术以营救第二个HDCT(HDCT2)(双重收获组DHG)。在HDCT1之前接受过化疗的患者中,HDCT1之后的干细胞收集效率低下且延迟。在SHG中,HDCT1和HDCT2之间的间隔短于DHG(中位62.5天vs 178.5天,P值= 0.002)。与HDCT1相比,HDCT2的血液学恢复延迟。但是,SHG和DHG之间的血液学恢复没有差异。在HDCT2期间记录到较高的治疗相关死亡率(TRM),但没有证据表明间隔时间越短导致TRM发生率越高(P值= 0.454)。在SHCT和DHG中HDCT2后2年无病生存的概率分别为66.7%和25.0%(P值= 0.031)。因此,为了在双HDCT中较早使用第二个HDCT,从而提高高危实体瘤患者的生存率,建议采用单收获方法而不是双收获方法.Bone Marrow Transplant(2003)31, 447-452。 doi:10.1038 / sj.bmt.1703869

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