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Engraftment syndrome after autologous peripheral blood progenitor cell transplantation in pediatric patients: a prospective evaluation of risk factors and outcome.

机译:小儿患者自体外周血祖细胞移植后的植入综合征:前瞻性评估危险因素和结果。

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We prospectively analyzed the incidence, risk factors and outcome of engraftment syndrome (ES) in 112 patients undergoing autologous peripheral blood progenitor cell transplantation with different malignancies between January 1999 and December 2003. The median age was 8 years (range 1-18). There were 73 males. There were 37 hematological neoplasias and 75 solid tumors. Disease status at transplantation was early in 49, intermediate in 15 and 48 in advanced phase. The median CD34+ cells infused was 4.6 x 10(6)/kg. With a median follow-up of 23 months (1-116 months), 38 patients developed ES. The cumulative incidence of ES was 34.5 +/- 4.5% and the event-free survival was 58.3 +/- 12%. There were no differences in the causes of death between patients with or without ES. A high number of CD34+ cells/kg infused, patients transplanted in early phase, the type of malignancy (solid tumor) and conditioning regimens other than busulfan based were significantly associated with ES in a multivariate analysis.
机译:我们前瞻性分析了1999年1月至2003年12月间112例接受不同恶性肿瘤的自体外周血祖细胞移植的患者的发生率,危险因素和移植物综合征的结果。中位年龄为8岁(范围1-18)。男73人。有37例血液肿瘤和75例实体瘤。移植时的疾病状况为49例早期,中期为15例,晚期为48例。注入的中值CD34 +细胞为4.6 x 10(6)/ kg。中位随访23个月(1-116个月),有38例患者发展为ES。 ES的累积发生率为34.5 +/- 4.5%,无事件生存率为58.3 +/- 12%。有或没有ES的患者之间的死亡原因没有差异。在多变量分析中,大量注入的CD34 +细胞/ kg,早期移植的患者,恶性肿瘤的类型(实体瘤)和除以白消安为基础以外的其他调理方案均与ES显着相关。

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