阿齐科死亡:可以提供单一剂量的德国肺结核新疗法

F. Stanzel
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摘要

贝伐单抗用于恶性胸腔积液(MPE)或恶性心包积液(MPCE)引起了越来越多的研究人员的兴趣,但贝伐单抗的精确给药方式尚不清楚。组织学或细胞学证实患有MPE或MPCE的非小细胞肺癌(NSCLC)患者被纳入研究,并在积液引流后使用低剂量的单次贝伐单抗(100mg)胸腔内或心包内注射进行治疗。本研究以肺癌症状量表(LCSS)、给药有效性和安全性作为评价参数。结果显示,治疗后患者肺癌相关症状较治疗前明显改善(LCSS评分494±78分vs 377±77分,mean±SD) (P < 0.001)。恶性积液得到很好的控制,MPE和MPCE的中位进展时间(TTP)分别为91天和111天。此外,除一名患者出现轻度头晕外,未观察到严重的副作用。综上所述,低剂量单次贝伐单抗(100mg)胸膜内或心包内注射治疗肺癌介导的恶性积液是有效且安全的,可迅速改善NSCLC患者的恶性积液相关症状和生活质量。
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Lungenkarzinom-assoziierte maligne Ergüsse: Neue Therapie könnte mit Einzeldosis Bevacizumab etabliert werden
The usage of bevacizumab for malignant pleural effusion (MPE) or malignant pericardial effusion (MPCE) has attracted increasing interest from researchers, but the precise ways of bevacizumab administration remain unknown. Patients with histologically or cytologically confirmed non-small-cell lung cancer (NSCLC) with MPE or MPCE were enrolled in the study and treated with a low dose of single bevacizumab (100 mg) intrapleurally or intrapericardially injected after the drainage of the effusions. The Lung Cancer Symptom Scale (LCSS), efficacy, and safety of drug administration were used as evaluation parameters in this study. The results indicated that lung cancer-related symptoms were significantly improved following treatment, compared with symptoms before the treatment (LCSS, score 494 ± 78 vs. score 377 ± 77, mean ± SD) (P < 0.001). Malignant effusions were well controlled, and the median time to progression (TTP) was 91 days and 111 days in MPE and MPCE, respectively. In addition, no severe side effects were observed, except in one patient with mild dizziness. In summary, the low dose of single bevacizumab (100 mg) with intrapleural or intrapericardial injection is effective and safe in the treatment of lung cancer-mediated malignant effusion, rapidly improving the malignant effusion-related symptoms and quality of life in patients with NSCLC.
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