首页> 外文期刊>Investigational new drugs. >BBR 3438, a novel 9-aza-anthrapyrazole, in patients with advanced gastric cancer: A phase II study group trial of the central European Society of Anticancer-Drug Research (CESAR).
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BBR 3438, a novel 9-aza-anthrapyrazole, in patients with advanced gastric cancer: A phase II study group trial of the central European Society of Anticancer-Drug Research (CESAR).

机译:BBR 3438,一种新型的9-氮杂-蒽吡唑,用于晚期胃癌患者:中欧抗癌药物研究协会(CESAR)的II期研究组试验。

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BBR 3438, a member of the 9-aza-anthrapyrazole family designed to decrease anthracycline dependent cardiotoxicity and to improve efficacy provided high in vivo activity in gastric carcinoma xenograft models. The present study was carried out to assess the efficacy and safety of BBR 3438 applied at a dose of 50 mg/m(2) four-weekly as an 1-hour infusion to pretreated patients with gastric cancer. Twenty-seven patients received at least one administration of BBR 3438. Lymph nodes and liver were the most common sites of metastases. A total of 94 cycles were administered (median 2, range 1-6). The main toxicity consisted of (worst per patient [%]; NCIC CTC grades 1/2/3/4) neutropenia 7/7/19/52 (one case of febrile neutropenia), stomatitis 15/19/4/-, nausea 22/26/7/-, vomiting 19/7/7/-, alopecia 15/33/-/-. Neutrophil nadir (520/mul) was reached after a median 15 days. The median time to recovery to
机译:BBR 3438是9-氮杂-蒽吡唑家族的成员,旨在减少蒽环类依赖性心脏毒性并提高疗效,在胃癌异种移植模型中提供了高体内活性。进行本研究以评估BBR 3438的疗效和安全性,每周四次以50 mg / m(2)的剂量向治疗过的胃癌患者灌胃1小时。 27名患者接受了至少一种BBR 3438的给药。淋巴结和肝脏是最常见的转移部位。总共进行了94个周期(中位数2,范围1-6)。主要毒性包括(每名患者中最差[%]; NCIC CTC分级1/2/3/4)中性粒细胞减少症7/7/19/52(1例高热性中性粒细胞减少症),口腔炎15/19/4 /-,恶心22/26/7 /-,呕吐19/7/7 /-,脱发15/33 /-/-。中位数15天后达到中性粒细胞最低点(520 / mul)。恢复到1级嗜中性白血球减少症的中位时间为13.5天。 BBR 3438的中位平均累积剂量为166.8 mg,中位剂量强度为48.8 mg / m(2)。左心室射血功能(LVEF)用多门血管造影术(MUGA)监测。基线和第2周期结束时的LVEF中值分别为67.5%和65%,并且没有患者显示LVEF降低。在25例可评估反应的患者中,未观察到缓解。四名患者(16%)病情稳定。进展中位时间为51天,中位总生存时间为64天。总体而言,证实了BBR 3438每周4次以50 mg / m(2)的剂量给药的可行性和耐受性,并且既未发现相关的LVEF降低,也未观察到心脏毒性的迹象。就抗肿瘤活性而言,发现BBR 3438在治疗胃癌方面无效。

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