首页> 外文期刊>Bone marrow transplantation >Etoposide induces more severe mucositis than CY when added to TBI as conditioning in allograft recipients receiving CsA and MTX.
【24h】

Etoposide induces more severe mucositis than CY when added to TBI as conditioning in allograft recipients receiving CsA and MTX.

机译:当在接受CsA和MTX的同种异体移植受者中加入调理TBI时,依托泊苷比CY引起更严重的粘膜炎。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Fractionated TBI and etoposide (FTBI-VP16) conditioning is effective therapy for patients receiving allogeneic stem cell transplants for ALL. One of the major dose-limiting toxicities with this regimen is mucositis although its effect on patients and hospital resources is not well described. To determine the severity of mucositis (WHO grade 3-4) experienced and assess resource utilisation, we compared the non-haematological toxicities of 38 patients receiving FTBI-VP16 with 104 patients receiving CY and TBI (CYTBI). FTBI-VP16 patients were more likely to develop severe mucositis (odds ratio (OR) 6.0 (95% confidence interval (CI) 1.36, 54.42), P<0.01) and its duration was longer (11.5 vs 8 days, P<0.01). Resource utilisation was considerably higher especially in the use and duration of i.v. narcotics and parenteral nutrition, nursing care requirements and plt-transfusion support. Patients receiving FTBI-VP16 conditioning are ideal candidates for new therapies to prevent or reduce the severity of mucositis.
机译:对于接受ALL的异基因干细胞移植的患者,分级TBI和依托泊苷(FTBI-VP16)调理是有效的疗法。尽管该药对患者和医院资源的影响尚未得到很好的描述,但该方案的主要剂量限制性毒性之一是粘膜炎。为了确定经历过的粘膜炎的严重程度(WHO 3-4级)并评估资源利用,我们比较了38例接受FTBI-VP16的患者和104例接受CY和TBI(CYTBI)的患者的非血液学毒性。 FTBI-VP16患者更有可能发展为重度粘膜炎(优势比(OR)6.0(95%置信区间(CI)1.36,54.42),P <0.01),病程更长(11.5 vs 8天,P <0.01) 。资源利用率大大提高,特别是在i.v的使用和持续时间方面。麻醉药品和肠胃外营养,护理要求和输血支持。接受FTBI-VP16调理的患者是预防或减轻粘膜炎严重程度的新疗法的理想人选。

著录项

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