摘要
目的:分析依硫磷酸治疗骨髓增生异常综合征(MDS)的临床疗效和不良反应,以指导MDS的治疗。方法:以amifostine、myelodysplasticsyndrome和therapuetics以及依硫磷酸和MDS为主题词在中英文数据库中检索所有依硫磷酸治疗MDS的临床研究。结果:共检索到24篇依硫磷酸治疗MDS的论文,一共有220例患者纳入研究,其中符合总疗效分析条件的患者一共有195例。在60例输血依赖患者当中,24例(14.7%)治疗后脱离输血,36例(60.0%)输血间隔延长一倍以上;140例粒细胞缺乏患者治疗后69例(49.3%)粒细胞上升超过一倍以上;在57例RAEB和RAEB-t患者当中,无一例幼稚细胞减少。不良反应主要有食欲下降61例(41.2%),恶心53例(35.8%),皮疹13例(8.8%),呕吐12例(8.1%),低血压11例(7.4%),疲劳感9例(6.1%),打喷嚏3例(2.0%),无症状低钙血症2例(1.3%),深静脉血栓2例(占1.3%)。结论:依硫磷酸可用于治疗细胞减少的难治性/复发性MDS。但对于血栓性疾病患者慎用。
Objective:To analyze the efficacy and side effects of amifostine in the treatment of myelodysplastic syndrome (MDS) in order to providing a basis for a decision model for the use of amifostine in MDS. Method: Amifostine, myelodysplastic syndrome and therapuetics were used as subjects to search all clinical papers related with amifostine in the treatment of MDS. Result:This Meta-analysis included 18 original articles with a total of 220 patients with MDS and there were 195 patients were suitable for the efficacy analysis. The average response rate for improving anemia was 36.8% (60) in 163 anemia patients treated with amifostine and 14.7%(24) patients were independent of transfusion among 60 transfusion dependent patients after treated with amifostine. Transfusion interval of another 36 patients (60%) doubled or more. The neutrophil number of 69(49.3%) patients increased significantly among 140 neutropenic patients. There was no blast decrease among all 57 RAEB and RAEB-t patients. Main side effects during and after amifostine treatment included decreased appetite (61, 41.2%), nausea (53, 35. 8%), pruritis (13, 8.8%), vomiting (12, 8. 1%), transient hypotension (11, 7. 4%), fatigue (9, 6. 1%), sneezing (3, 2.0%), asymptom hypocalcemia (2, 1.3%), deep venous thrombosis (2, 1.3%). Conclusion:Amifostine could be safely used in the treatment of relapse and/or refratory MDS. Amifostine may be not suitable for the patients with thrombosis.
出处
《临床血液学杂志》
CAS
2009年第1期6-9,14,共5页
Journal of Clinical Hematology
基金
国家自然科学基金项目(No:30772597)
军队"十一五"项目(No:2006B)1