首页> 外文期刊>British Journal of Haematology >High event-free survival rate with minimum-dose-anthracycline treatment in childhood acute promyelocytic leukaemia: a nationwide prospective study by the Japanese Paediatric Leukaemia/Lymphoma Study Group
【24h】

High event-free survival rate with minimum-dose-anthracycline treatment in childhood acute promyelocytic leukaemia: a nationwide prospective study by the Japanese Paediatric Leukaemia/Lymphoma Study Group

机译:儿童急性早幼粒细胞白血病使用最小剂量的蒽环类药物治疗的无事件生存率高:日本小儿白血病/淋巴瘤研究小组的一项全国性前瞻性研究

获取原文
获取原文并翻译 | 示例
           

摘要

We evaluated the efficacy of treatment using reduced cumulative doses of anthracyclines in children with acute promyelocytic leukaemia (APL) in the Japanese Paediatric Leukaemia/Lymphoma Study Group AML-P05 study. All patients received two and three subsequent courses of induction and consolidation chemotherapy respectively, consisting of all-trans retinoic acid (ATRA), cytarabine and anthracyclines, followed by maintenance therapy with ATRA. Notably, a single administration of anthracyclines was introduced in the second induction and all consolidation therapies to minimize total doses of anthracycline. The 3-year event-free (EFS) and overall survival rates for 43 eligible children were 836% [95% confidence interval (CI): 686-918%] and 907% (95% CI: 771-964%), respectively. Although two patients died of intracranial haemorrhage or infection during induction phases, no cardiac adverse events or treatment-related deaths were observed during subsequent phases. Patients not displaying M1 marrow after the first induction therapy, or those under 5years of age at diagnosis, showed inferior outcomes (3-year EFS rate; 333% (95% CI: 193-676%) and 546% (95% CI: 229-780%), respectively). In conclusion, a single administration of anthracycline during each consolidation phase was sufficient for treating childhood APL. In younger children, however, conventional ATRA and chemotherapy may be insufficient so that alternative therapies should be considered.
机译:我们在日本小儿白血病/淋巴瘤研究小组AML-P05研究中评估了减少剂量的蒽环类药物治疗急性早幼粒细胞白血病(APL)的疗效。所有患者均分别接受了两个和三个疗程的诱导和巩固化疗,包括全反式维甲酸(ATRA),阿糖胞苷和蒽环类药物,然后进行ATRA维持治疗。值得注意的是,在第二次诱导中引入了蒽环类药物的单次给药,并采用所有巩固疗法以使蒽环类药物的总剂量最小化。 43名合格儿童的3年无事件(EFS)和总生存率分别为836%[95%置信区间(CI):686-918%]和907%(95%CI:771-964%) 。尽管有两名患者在诱导阶段死于颅内出血或感染,但在随后的阶段未观察到心脏不良事件或与治疗相关的死亡。首次诱导治疗后未显示M1骨髓的患者或诊断时年龄小于5岁的患者表现较差(3年EFS率; 333%(95%CI:193-676%)和546%(95%CI:分别为229-780%)。总之,在每个巩固阶段单用蒽环类药物就足以治疗儿童期APL。然而,对于年幼的儿童,常规的ATRA和化疗可能不足,因此应考虑其他疗法。

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号