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首页> 外文期刊>Annals of hematology >The clinical features of fatal cyclophosphamide-induced cardiotoxicity in a conditioning regimen for allogeneic hematopoietic stem cell transplantation (allo-HSCT)
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The clinical features of fatal cyclophosphamide-induced cardiotoxicity in a conditioning regimen for allogeneic hematopoietic stem cell transplantation (allo-HSCT)

机译:异基因造血干细胞移植(allo-HSCT)调理方案中致命性环磷酰胺引起的心脏毒性的临床特征

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摘要

Cyclophosphamide (CY) cardiotoxicity induces a rare lethal complication associated with its use. The minimum dose for cardiac toxicity is still not known, although there are no reports of CY toxicity at doses of less than 100 mg/kg. There are few studies of CY cardiotoxicity that included a large number of patients who received high-dose CY for conditioning for allogeneic stem cell transplant (allo-HSCT). To elucidate the clinical course, complications, true incidence, and risk factors, the cardiac events of 811 patients who received more than a total of 100 mg/kg of CY as conditioning for allo-HSCT were analyzed. Twelve of 811 recipients (1.5 %) developed fatal cardiac failure induced by CY at a median of 4 (range 2-8) days after the first administration of CY. Regarding the dose of CY, 8.5, 1.2, and 0 % of the patients developed cardiac failure among the patients treated with a total of 200, 120, and 100 mg/kg CY, respectively. On echocardiography, the E/A ratio shows diastolic dysfunction but not the ejection fraction changed in the early course. Moreover, a short time to the first symptom after the administration of CY tended to be associated with early death (p = 0.09). Eleven patients died from progressive acute cardiac failure at day 7 (5-30) after the first administration of CY, and only one patient survived. In summary, fatal CY cardiotoxicity with allo-HSCT is a rare complication, but it is associated with high mortality. The possibility of CY-induced cardiotoxicity must be considered early after the administration of CY.
机译:环磷酰胺(CY)的心脏毒性会引起罕见的致死性并发症。尽管尚无低于100 mg / kg剂量的CY毒性的报道,但对心脏毒性的最小剂量仍然未知。 CY心脏毒性的研究很少,其中包括大量接受高剂量CY进行同种异体干细胞移植(allo-HSCT)调理的患者。为了阐明临床过程,并发症,真实发生率和危险因素,分析了811名接受总剂量超过100 mg / kg CY的患者的心脏事件,作为Allo-HSCT的条件。 811位接受者中有十二位(占1.5%)在首次服用CY后的4天(2-8天)中位数出现了由CY引起的致命性心力衰竭。关于CY的剂量,在分别以200、120和100 mg / kg CY治疗的患者中,分别有8.5%,1.2%和0%的患者出现心力衰竭。在超声心动图上,E / A比显示舒张功能障碍,但射血分数在早期病程中未改变。而且,CY给药后第一症状出现的时间短往往与早期死亡相关(p = 0.09)。首次给予CY后第7天(5-30),有11名患者死于进行性急性心力衰竭,只有一名患者存活。总之,同种异体造血干细胞移植致命的CY心脏毒性是一种罕见的并发症,但与高死亡率相关。 CY给药后应尽早考虑CY引起的心脏毒性的可能性。

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