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JAMA:贝伐单抗与遗传性血管疾病患者心输出量改善有关

2012-03-08 MedSci MedSci原创

近日,国际医学杂志《美国医学会杂志》JAMA上的一项研究揭示,在一项包括有25名罹患遗传性出血性毛细血管扩张症(一种遗传性疾病,它会导致血管的异常)并因为这一疾病而有严重肝累及的病人的研究中,那些接受药物贝伐单抗的病人的心输出量会得到改善,其发生鼻衄的时间会缩短而且次数减少;而鼻衄是罹患这种疾病者的一种可能会威胁生命的并发症。 遗传性出血性毛细血管扩张症(HHT)是一种显性的遗传性血管疾病;

近日,国际医学杂志《美国医学会杂志》JAMA上的一项研究揭示,在一项包括有25名罹患遗传性出血性毛细血管扩张症(一种遗传性疾病,它会导致血管的异常)并因为这一疾病而有严重肝累及的病人的研究中,那些接受药物贝伐单抗的病人的心输出量会得到改善,其发生鼻衄的时间会缩短而且次数减少;而鼻衄是罹患这种疾病者的一种可能会威胁生命的并发症。

遗传性出血性毛细血管扩张症(HHT)是一种显性的遗传性血管疾病;它会影响多种器官,其中包括肺、胃肠道、肝和脑。根据文章的背景资料,人们观察到,有高达74%的这种病人会有肝脏的累及,而肝血管畸形会导致严重的并发症,其中包括高输出量心力衰竭。

法国Bron市LouisPradel医院的Sophie Dupuis-Girod, M.D., Ph.D.及其同事在有严重的与高心输出量有关的肝脏形式的HHT患者中对药物贝伐单抗的功效进行了分析。贝伐单抗是一种抗血管内皮生长因子的治疗药物,人们认为它可能会对治疗HHT有效。该单一中心的2期试验包括了被确诊有HHT、严重肝累及以及与HHT有关的高心脏指数的25名患者。参与者每14天会接受一次贝伐单抗治疗,他们总共会接受6次贝伐单抗的注射。治疗的全部时间为2.5个月;病人在治疗开始后会被随访长达6个月。该研究的主要检测结果是第一次注射后3个月时的由超声心动图评估的心输出量。

在24名可重新再读其超声心动图的病人中,这24名患者中有反应者达20人,其中心指数恢复正常者(有完全的反应)有3人,有部分反应者达17人,无反应者有4人。在治疗开始时的心指数中位数(中点)在治疗3个月后显著降低。在治疗后6个月时的心指数中位数比治疗前有了显著的下降。病人在被纳入研究时其平均鼻衄(鼻出血)时间为每月221分钟,但其在治疗开始后3个月时(134分钟)和6个月时(43分钟)则有了显著的减少。他们的生活品质也有了显著的改善。

Bevacizumab in Patients With Hereditary Hemorrhagic Telangiectasia and Severe Hepatic Vascular Malformations and High Cardiac Output

Sophie Dupuis-Girod, MD, PhD; Isabelle Ginon, MD; Jean-Christophe Saurin, MD, PhD; Denis Marion, MD; Elsa Guillot, MD; Evelyne Decullier, PhD; Adeline Roux, MsC; Marie-France Carette, MD, PhD; Brigitte Gilbert-Dussardier, MD, PhD; Pierre-Yves Hatron, MD, PhD; Pascal Lacombe, MD, PhD; Bernard Lorcerie, MD, PhD; Sophie Rivière, MD; Romain Corre, MD; Sophie Giraud, MD, PhD; Sabine Bailly, PhD; Gilles Paintaud, MD, PhD; David Ternant, MD; Pierre-Jean Valette, MD, PhD; Henri Plauchu, MD, PhD; Frédéric Faure, MD, PhD

Context:The only treatment available to restore normal cardiac output in patients with hereditary hemorrhagic telangiectasia (HHT) and cardiac failure is liver transplant. Anti–vascular endothelial growth factor treatments such as bevacizumab may be an effective treatment.

Objectives:To test the efficacy of bevacizumab in reducing high cardiac output in severe hepatic forms of HHT and to assess improvement in epistaxis duration and quality of life.

Design, Setting, and Patients:Single-center, phase 2 trial with national recruitment from the French HHT Network. Patients were 18 to 70 years old and had confirmed HHT, severe liver involvement, and a high cardiac index related to HHT.

Intervention:Bevacizumab, 5 mg per kg, every 14 days for a total of 6 injections. The total duration of the treatment was 2.5 months; patients were followed up for 6 months after the beginning of the treatment.

Main Outcome Measure:Decrease in cardiac output at 3 months after the first injection, evaluated by echocardiography. Results A total of 25 patients were included between March 2009 and November 2010. Of the 24 patients who had echocardiograms available for reread, there was a response in 20 of 24 patients with normalization of cardiac index (complete response [CR]) in 3 of 24, partial response (PR) in 17 of 24, and no response in 4 cases. Median cardiac index at beginning of the treatment was 5.05 L/min/m2 (range, 4.1-6.2) and significantly decreased at 3 months after the beginning of the treatment with a median cardiac index of 4.2 L/min/m2 (range, 2.9-5.2; P < .001). Median cardiac index at 6 months was significantly lower than before treatment (4.1 L/min/m2; range, 3.0-5.1). Among 23 patients with available data at 6 months, we observed CR in 5 cases, PR in 15 cases, and no response in 3 cases. Mean duration of epistaxis, which was 221 minutes per month (range, 0-947) at inclusion, had significantly decreased at 3 months (134 minutes; range, 0-656) and 6 months (43 minutes; range, 0-310) (P = .008). Quality of life had significantly improved. The most severe adverse events were 2 cases of grade 3 systemic hypertension, which were successfully treated.

Conclusion:In this preliminary study of patients with HHT associated with severe hepatic vascular malformations and high cardiac output, administration of bevacizumab was associated with a decrease in cardiac output and reduced duration and number of episodes of epistaxis.

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  美国匹兹堡市国家外科辅助乳腺与肠道项目   背景 (研究)已显示,在有转移性乳腺癌的患者中,在紫杉烷类的基础上加上贝伐单抗、抗代谢药物卡培他滨及吉西他滨可以改善(患者)转归。该项试验的主要目的是确定在患有可手术的、人表皮生长因子受体2(HER2)-阴性乳腺癌的女性中,在多西他赛序贯多柔比星及环磷酰胺的新辅助化疗基础上,加上卡培他滨或吉西他滨是否可增加病理学完全缓解率,以及确定在这些化疗方案中

NEJM:新辅助化疗和贝伐单抗治疗HER2-阴性乳腺癌

  德国乳腺组和妇产科肿瘤—乳腺联合(Arbeisgemeinschaft)研究组   背景 贝伐单抗是一种抗血管内皮生长因子A的单克隆抗体,已在患有人表皮生长因子受体2(HER2)-阴性转移性的乳腺癌患者中显示出了临床疗效。我们在患有早期乳腺癌的患者中,评估了在新辅助化疗基础上加用贝伐单抗的疗效和安全性,根据病理学完全缓解率(在乳房和腋淋巴结中无侵润性和导管内病变)来检测疗效。   方法 我

贝伐单抗能增加癌症患者的重症蛋白尿风险

采用化学治疗药物(贝伐单抗,是中和血管内皮生长因子的人源化抗体)治疗可导致蛋白尿和肾功能损害。尚未完全理解肾功能不良事件的风险因素和临床结果。我们对已发表的随机、对照试验进行一项系统性回顾和荟萃分析,以评估应用贝伐单抗治疗引起重症蛋白尿的整体风险。我们分析了来自16个研究(包括12,268例患有多种肿瘤的患者)的数据。应用贝伐单抗治疗的大量(3或4级)蛋白尿发病率为2.2%(95%置信区间 [CI

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