首页> 美国卫生研究院文献>SpringerPlus >Significant dose Escalation of Idarubicin in the treatment of aggressive Non- Hodgkin Lymphoma leads to increased hematotoxicity without improvement in efficacy in comparison to standard CHOEP-14: 9-year follow up results of the CIVEP trial of the DSHNHL
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Significant dose Escalation of Idarubicin in the treatment of aggressive Non- Hodgkin Lymphoma leads to increased hematotoxicity without improvement in efficacy in comparison to standard CHOEP-14: 9-year follow up results of the CIVEP trial of the DSHNHL

机译:与标准CHOEP-14相比依达比星在侵袭性非霍奇金淋巴瘤的治疗中显着剂量升高导致血液毒性增加但疗效没有改善:DSHNHL的CIVEP试验的9年随访结果

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摘要

BackgroundDose escalation and modification of CHOP has improved the prognosis of patients with aggressive lymphoma; even in the rituximab era, dose escalation for high-risk patients is exploited and frequently limited by drug toxicity. Idarubicin (Id) is a 4-demethoxy anthracycline analogue of daunorubicin with activity against lymphoma and has been reported to cause less cardiotoxicity than other anthracylines. The aim of this study was to replace doxorubicine with idarubicin in the CHOEP regimen and to find the maximum tolerable dose (MTD) of idarubicin based on hematotoxicity.
机译:背景剂量的增加和CHOP的改变改善了侵袭性淋巴瘤患者的预后。即使在利妥昔单抗时代,也利用了高危患者的剂量递增,并经常受到药物毒性的限制。依达比星(Id)是柔红霉素的4-脱甲氧基蒽环类类似物,具有抗淋巴瘤的活性,据报道其心脏毒性比其他蒽环类更少。这项研究的目的是在CHOEP方案中用阿达比星替换阿霉素,并根据血液毒性来找到阿达比星的最大耐受剂量(MTD)。

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