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Recombinant Human Erythropoietin Treatment for Chemotherapy-related Anemia in Children

机译:重组人促红细胞生成素治疗儿童化疗相关性贫血

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Objective.? The efficacy and safety of recombinant human erythropoietin (rHuEPO) treatment in chemotherapy-induced anemia in children were investigated. rHuEPO is used to treat chemotherapy-induced anemia. Several studies recommend 150 to 300 IU/kg rHuEPO for 2 to 8 months. There are only a few controlled trials in children and no precise data about the optimal dose and duration of rHuEPO treatment is available.Patients and Methods.? Thirty-four patients receiving chemotherapy for treatment of their solid tumors between October 1996 and June 1997 were included in this study. Patients were randomly selected for each group. The male/female ratio was 20/14, and the median age was 5 years (range, 1–16 years). They had normal hemoglobin levels at the time of diagnosis. When hemoglobin levels decreased to levels lower than 10 g/dL, rHuEPO (150 IU/kg/d, 3 times a week, subcutaneously) was given to 17 patients for 2 months. Their renal, liver, and pulmonary functions were normal. None of the patients had hematologic disease. We did not use any other drugs such as iron or granulocyte colony-stimulating factor. There were 17 patients in the control group. Fifteen patients got chemotherapy regimens including cisplatin (CDDP), but 19 were treated with regimens without CDDP. At the end of rHuEPO treatment, all patients were examined in terms of transfusion requirements and rate of change in hemoglobin levels.Results.? One patient in the study group needed a blood transfusion, whereas 8 patients needed a transfusion in the control group. Patients in the study group had less transfusion requirements compared with the control group. The mean hemoglobin levels before and after the study were 8.48 ± 0.98 g/dL and 8.41 ± 1.65 g/dL in the control group and 8.50 ± 0.85 g/dL and 10.21 ± 2.14 g/dL in the rHuEPO group, respectively. Optimal hemoglobin increments began in 4 weeks and continued during treatment. CDDP-receiving and CDDP-nonreceiving groups did not have any difference in pretreatment serum erythropoietin levels. rHuEPO treatment was more effective in patients treated with non-CDDP regimens. Mean hemoglobin level increased from 8.68 ± 0.73 g/dL to 10.26 ± 1.84 g/dL in 9 patients treated with non-CDDP chemotherapy regimens in the erythropoietin group, although it increased from 8.28 ± 0.97 g/dL to 10.15 ± 2.5 g/dL in 8 patients treated with CDDP-containing regimens in the erythropoietin group. rHuEPO caused high blood pressure in only 1 patient that resolved spontaneously after cessation of erythropoietin treatment for a week.Conclusion.? rHuEPO treatment (150 IU/kg/d 3 times a week) is effective and safe in children with chemotherapy-induced anemia. It decreases blood transfusion requirements in solid tumor patients. Our results show that the response to rHuEPO in CDDP-induced anemia is less than the response in non-CDDP receiving patients. Higher doses may be necessary in patients using CDDP.
机译:目的。?研究了重组人促红细胞生成素(rHuEPO)治疗儿童化疗性贫血的疗效和安全性。 rHuEPO用于治疗化疗引起的贫血。多项研究建议在2到8个月内使用150到300 IU / kg rHuEPO。在儿童中只有少数对照试验,尚无关于rHuEPO治疗的最佳剂量和持续时间的确切数据。该研究包括1996年10月至1997年6月期间接受化疗治疗实体瘤的34名患者。每组随机选择患者。男女比例为20/14,中位年龄为5岁(范围为1-16岁)。诊断时他们的血红蛋白水平正常。当血红蛋白水平降至低于10 g / dL时,对17例患者进行了2个月的rHuEPO(150 IU / kg / d,每周3次,皮下注射)。他们的肾,肝和肺功能正常。没有患者有血液系统疾病。我们没有使用任何其他药物,例如铁或粒细胞集落刺激因子。对照组17例。 15例患者接受了包括顺铂(CDDP)在内的化疗方案,但19例接受了无CDDP方案的治疗。在rHuEPO治疗结束时,检查了所有患者的输血需求和血红蛋白水平的变化率。研究组中一名患者需要输血,而对照组中有八名患者需要输血。与对照组相比,研究组患者的输血需求较少。研究之前和之后的平均血红蛋白水平在对照组中分别为8.48±0.98 g / dL和8.41±1.65 g / dL,在rHuEPO组中分别为8.50±0.85 g / dL和10.21±2.14 g / dL。最佳血红蛋白增量在4周内开始,并在治疗期间持续不断。 CDDP接受组和CDDP非接受组在治疗前血清促红细胞生成素水平上没有任何差异。在非CDDP方案治疗的患者中,rHuEPO治疗更有效。促红细胞生成素组中9位接受非CDDP化疗方案的患者的平均血红蛋白水平从8.68±0.73 g / dL增加到10.26±1.84 g / dL,尽管从8.28±0.97 g / dL增加到10.15±2.5 g / dL在促红细胞生成素组中接受CDDP方案治疗的8例患者中。 rHuEPO仅导致1名患者的高血压,该患者在停止使用促红细胞生成素治疗一周后自发缓解。 rHuEPO治疗(每周3次150 IU / kg / d)对患有化疗引起的贫血的儿童有效且安全。它减少了实体瘤患者的输血需求。我们的结果表明,在CDDP引起的贫血中,对rHuEPO的反应小于未接受CDDP的患者。使用CDDP的患者可能需要更高剂量。

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