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作 者:张诚[1] 陈幸华[1] 张曦[1] 高蕾[1] 刘林[1] 孔佩艳[1] 刘红[1] 彭贤贵[1] 王武[1] 王庆佘[1]
机构地区:[1]第三军医大学新桥医院血液科,重庆400037
出 处:《中国医师杂志》2007年第10期1297-1300,共4页Journal of Chinese Physician
基 金:重庆市医学重点学科建设基金资助项目(2006C028)
摘 要:目的评价大剂量化疗、自体外周血干细胞移植、生物治疗,长间歇维持化疗序贯治疗成人急性非淋巴细胞白血病(ANLL)的疗效。方法32例成人急性非淋巴细胞白血病患者首次缓解并经3个周期大剂量阿糖胞苷强化治疗后,行自体外周血干细胞移植,预处理方案采用MAC、CEAC等,造血重建后予以大剂量IL-2生物治疗4个疗程,之后每3~4个月予以长间歇化疗1次,共维持2年,常用方案包括TA、MA、HEA等。结果32例患者移植后均成功重建造血,无一例移植相关死亡。长间歇维持化疗满2年的12例中,有8例存活;存活中位时间为确诊后1268(953-1926)d,移植后986(725-1742)d,平均生存时间为1475.7 d,3年无病存活率为(66.7±8.1)%;其余维持化疗还未到2年的20例患者中,有2例复发(10.0%),其中1例死亡(5.0%),其余18例至今病情稳定。结论大剂量化疗、自体外周血干细胞移植、生物治疗、长间歇维持化疗序贯治疗成人急性非淋巴细胞白血病,治疗相关死亡率低,无病生存率较高,可作为改善成人ANLL治疗效果的重要措施。Objective To evaluate the clinical efficacy of high - dose hemotherapy, auto - peripheral blood stem cell transplantation (auto- PBSCT) and long -interval maintenance therapy in adult acute nonlymphoblastic leukemia (ANLL). Methods Thirty -two adult ANLL patients received auto-PBSCT after first remission induction and three courses high-dose Ara - e treatment. After auto-PBSCT, patients received high dose IL-2 (100WU/d) treatmemt for 28 days and long-interval maintenance therapy per 3 -4 months. MAC and CEAC are the frequently used treatment prescription. Results Thirty-two adult ANLL patients had rapid hematopoietie reeonstitution after auto-PBSCT. There was no hematopoietic stem cell transplantation related death. After two years of long-interval maintenance therapy, eight of twelve patients were alive. The median follow-up duration was 1268 (953 - 1926) days after diagnosis or 986 (725 - 1742) days after auto-PBSCT, and the average live time was 1475.7 days. The 3 year disease - free survival (DFS) was (66.7 ± 8. 1 ) %. Among the other twenty patients who are being still for long-interval maintenance therapy, two patients were relapse (10. 0% ) including one died patient(5.0% ). Conclusion It suggested that auto-PBSCT combined with long-interval maintenance therapy could be used as an important treatment for adult acute nonlymphoblastie leukemia owing to its low HSCT related death and long DFS.
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