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首页> 外文期刊>Neurology: Official Journal of the American Academy of Neurology >Cardiotoxicity and other adverse events associated with mitoxantrone treatment for MS.
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Cardiotoxicity and other adverse events associated with mitoxantrone treatment for MS.

机译:毒性和其他相关的不良事件与米托蒽醌治疗MS。

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BACKGROUND: Mitoxantrone is used for aggressive multiple sclerosis (MS), but concerns about safety, including cardiotoxicity and other laboratory measures, prevail. OBJECTIVE: To evaluate the incidence and potential predictors of adverse events associated with mitoxantrone at the MS Clinic, University of British Columbia, Canada. METHODS: Retrospective review of patients treated with mitoxantrone by standard protocol; maximum cumulative dose = 120 mg/m(2). Left ventricular ejection fraction (LVEF) was measured with regular multiple-gated acquisition (MUGA) scans; blood cell counts and biochemical liver tests were performed before infusions. Generalized estimating equations were used to examine potential predictors of adverse events (graded according to the Common Toxicity Criteria, version 4) in patients with normal baseline and > or =1 follow-up MUGA or laboratory assessment. RESULTS: All 163 patients (58% women) treated with mitoxantrone from 1999 to 2007 were reviewed. Mean baseline age was 41.9 (SD 10.8) years, cumulative dose was 59.7 (SD 26.0) mg/m(2), and median follow-up duration was 14 months (maximum 6.5 years). By study end, 14% developed de novo cardiotoxicity (grade > or =2) as measured by decreased LVEF, 27% neutropenia (grade > or =1), 15% anemia (grade > or =1), and 15% liver toxicity (grade > or =1). Possible predictors of adverse events included sex, age, disease duration, and cumulative dose; only women exposed to a higher cumulative dose were at a greater risk of anemia (adjusted odds ratio 1.26, 95% confidence interval 1.08-1.48 per 10 mg/m(2)). CONCLUSIONS: Based on cardiac and laboratory assessments, mitoxantrone was reasonably well tolerated. However, cardiotoxicity was evident after doses well below current maximum recommended levels. A dose-response effect was not apparent. Findings emphasize the importance of monitoring; the long-term effects of mitoxantrone in multiple sclerosis require investigation.
机译:背景:米托蒽醌用于咄咄逼人多发性硬化(MS),但担忧安全,包括毒性和其他实验室措施,获胜。评估发病率和潜在的预测因子与米托蒽醌相关的不良事件女士诊所,英属哥伦比亚大学,加拿大。米托蒽醌治疗标准协议;最大累积剂量= 120毫克/米(2)。心室射血分数(LVEF)测量与普通multiple-gated收购(蒙加)扫描;测试之前进行注资。广义估计方程被用来检查不良事件的潜在因素(根据常见毒性分级标准版本4)患者的正常基线和> = 1后续蒙加或实验室评估。米托蒽醌治疗从1999年到2007年回顾。年,累积剂量为59.7(标准差26.0)毫克/ m(2),平均随访时间为14个月(最大6.5年)。开发新创毒性(> = 2)级以LVEF减少、中性粒细胞减少27%(> = 1)级,15%贫血(> = 1)级,和15%的肝脏毒性(> = 1)级。预测不良事件包括性别、年龄、疾病持续时间和累积剂量;暴露于更高的累积剂量在贫血的风险更高(调整后的优势比为1.26,95%置信区间1.08 - -1.48每10毫克/米(2))。实验室评估、米托蒽醌合理的耐受性良好。毒性剂量远低于后明显目前最大的推荐水平。剂量反应的影响不明显。强调监测的重要性;米托蒽醌在多个的长期影响硬化需要调查。

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