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米托蒽醌的心脏评估。

Cardiac evaluation of mitoxantrone.

作者信息

Unverferth D V, Unverferth B J, Balcerzak S P, Bashore T A, Neidhart J A

出版信息

Cancer Treat Rep. 1983 Apr;67(4):343-50.

PMID:6850653
Abstract

Mitoxantrone is a synthetic anthraquinone that was developed through the doxorubicin analog program in hopes of retaining anticancer activity with less cardiotoxicity. This study evaluated 18 patients receiving mitoxantrone with serial noninvasive tests of left ventricular function and with endomyocardial biopsy. The echocardiograms and systolic time intervals demonstrated a trend to deterioration that did not achieve statistical significance. However, the nuclear angiographic ejection fraction significantly decreased from 61% +/- 6% (means +/- SD) at baseline to 58% +/- 5% (P less than 0.05) after 48 mg/m2 of mitoxantrone. The endomyocardial biopsies revealed tubular swelling, degeneration of mitochondria, minimal chromatin clumping, and myofibrillar lysis. This study has revealed mild but definite impairment of cardiac function and mild changes of myocardial morphology during mitoxantrone therapy. Although mitoxantrone is an effective chemotherapeutic agent, a direct comparison of mitoxantrone with doxorubicin is necessary to compare relative therapeutic to cardiotoxic ratios.

摘要

米托蒽醌是一种合成蒽醌,它是通过阿霉素类似物项目开发的,以期在保持抗癌活性的同时降低心脏毒性。本研究对18例接受米托蒽醌治疗的患者进行了左心室功能的系列非侵入性检测和心内膜活检。超声心动图和收缩期时间间期显示有恶化趋势,但未达到统计学意义。然而,核素血管造影射血分数在给予48mg/m²米托蒽醌后,从基线时的61%±6%(均值±标准差)显著降至58%±5%(P<0.05)。心内膜活检显示有管状肿胀、线粒体变性、少量染色质凝聚和肌原纤维溶解。本研究揭示了米托蒽醌治疗期间心脏功能有轻度但明确的损害以及心肌形态有轻度改变。尽管米托蒽醌是一种有效的化疗药物,但有必要将米托蒽醌与阿霉素进行直接比较,以比较相对治疗与心脏毒性比率。

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