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首页> 外文期刊>Future oncology >Phase II trial evaluating the efficacy and safety of the anti-CD20 monoclonal antibody obinutuzumab in patients with marginal zone lymphoma
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Phase II trial evaluating the efficacy and safety of the anti-CD20 monoclonal antibody obinutuzumab in patients with marginal zone lymphoma

机译:期II试验评估抗CD20单克隆抗体Obinutuzumab在边缘区淋巴瘤患者中的疗效和安全性

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摘要

Marginal zone lymphoma (MZL) belongs to the group of indolent B-cell non-Hodgkin's lymphomas, which is characterized by an indolent course. In this mostly elderly patient population, the development of chemotherapy-free approaches is of particular interest. In this situation, single-agent treatment with the next-generation anti-CD20 antibody obinutuzumab is an attractive approach, which promises high efficacy without major toxicity. We describe here an open-label, multicentric Phase II trial evaluating the efficacy and safety of obinutuzumab in de novo MZL patients, who are treatment naive for systemic therapy and not eligible for or failed local treatment. ClinicalTrials.gov identifier NCT03322865
机译:边缘区淋巴瘤(MZL)属于惰性B细胞非霍奇金淋巴瘤的淋巴瘤,其特征在于惰性课程。 在这最长的老年患者人口中,无需化疗的方法的发展是特别的兴趣。 在这种情况下,用下一代抗CD20抗体obInutuzumab的单孕处理是一种吸引人的方法,这承诺没有重大毒性的高效性。 我们在这里描述了一个开放标签,多中心第二期试验评估Obinutuzumab在De Novo Mzl患者中的疗效和安全性,他是全身治疗的治疗Naive,不符合局部治疗或失败。 ClinicalTrials.gov标识符NCT03322865

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