...
首页> 外文期刊>Journal of cancer survivorship: research and practice >Late cardiotoxicity after low dose of anthracycline therapy for acute lymphoblastic leukemia in childhood
【24h】

Late cardiotoxicity after low dose of anthracycline therapy for acute lymphoblastic leukemia in childhood

机译:小剂量蒽环类药物治疗儿童急性淋巴细胞白血病后的晚期心脏毒性

获取原文
获取原文并翻译 | 示例

摘要

Introduction: Late cardiotoxicity is a known complication of anthracycline therapy but the long-term effects of low cumulative doses are not well documented. We studied late cardiotoxicity in survivors of childhood acute lymphoblastic leukemia (ALL) treated with low anthracycline doses 10 to 20 years earlier. Methods: Seventy-seven ALL survivors who received a cumulative anthracycline dose 250 mg/m 2 and were at least 10 years after treatment were evaluated for signs of clinical heart failure. Cardiac function was assessed by echocardiography including tissue Doppler measurements of the septal mitral annulus in 37 ALL survivors 10. 6-18. 3 years (median 13. 3 years) after anthracycline treatment with cumulative doses of 180 (n = 19) or 240 mg/m 2 (n = 18). The control group consisted of 30 healthy volunteers matched for age, sex, BSA, and BMI. Results: No clinical relevant cardiotoxicity was found. Left ventricular shortening fraction (SF) was significantly reduced in male ALL survivors. Three of the 19 male ALL survivors had an SF below 30%. Male ALL survivors showed a significantly lower early filling velocity to atrial contraction velocity ratio but myocardial velocity during early filling was comparable between patients and controls. ALL survivors had a significantly longer isovolumetric relaxation time (IVRT). Thirty percent of the ALL survivors have an abnormal IVRT compared to the normal range of the controls. Conclusion and implications for cancer survivors: At a median of 13. 3 years after exposure to cumulative doses of anthracyclines of 180 or 240 mg/m 2, no clinical relevant cardiotoxicity was found but subclinical cardiac abnormalities were present in 30% of the patients.
机译:简介:晚期心脏毒性是蒽环类药物治疗的一种已知并发症,但是低累积剂量的长期作用尚未得到充分证明。我们研究了使用低蒽环类药物剂量治疗10至20年以前的儿童急性淋巴细胞白血病(ALL)幸存者的晚期心脏毒性。方法:对接受累积蒽环类药物剂量<250 mg / m 2且治疗后至少10年的77名ALL幸存者进行临床心力衰竭迹象的评估。通过超声心动图评估心脏功能,包括对37位ALL幸存者10、6-18中二尖瓣环间隔进行组织多普勒测量。蒽环类药物治疗后3年(中位数13年。3年),累积剂量为180(n = 19)或240 mg / m 2(n = 18)。对照组由30位年龄,性别,BSA和BMI相匹配的健康志愿者组成。结果:未发现临床相关的心脏毒性。男性ALL幸存者的左心室缩短分数(SF)明显降低。 19名男性ALL幸存者中有3名的SF低于30%。男性ALL幸存者显示出较低的早期充盈速度与心房收缩速度之比,但早期充盈期间的心肌速度在患者和对照组之间相当。所有幸存者的等容松弛时间(IVRT)均明显更长。与对照组的正常范围相比,所有幸存者中有30%的IVRT异常。结论和对癌症幸存者的影响:在接触累积剂量为180或240 mg / m 2的蒽环类药物后的中位数13. 3年,未发现临床相关的心脏毒性,但30%的患者存在亚临床心脏异常。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 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