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Ipilimumab activity in advanced uveal melanoma

机译:Ipilimumab在晚期葡萄膜黑色素瘤中的活性

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摘要

Uveal melanoma (UM) is a rare disease with a distinct molecular profile. About half of the patients with UM eventually develop metastatic disease. The prognosis of these patients remains poor. Treatment options are limited and none of them have been able to show a survival benefit. Ipilimumab was the first agent to show a survival benefit in patients with cutaneous melanoma in a randomized trial; however, there is limited published evidence for its role in the management of advanced UM. Here, we report our experience of ipilimumab in five patients with advanced UM treated at an academic cancer centre in the UK. Two patients had durable stable disease and three developed progressive disease. Of the patients with stable disease, one maintained disease control at 11 months from the commencement of treatment with ~10% reduction in tumour volume compared with the baseline, and the second patient progressed after 15 months. We also examined the tumour kinetics and response patterns that resembled that of ipilimumab in cutaneous melanoma. Given the lack of randomized trial data, our findings indicate that ipilimumab might be a reasonable treatment option for patients with advanced UM.
机译:葡萄膜黑色素瘤(UM)是一种罕见的疾病,具有独特的分子特征。大约一半的UM患者最终发展成转移性疾病。这些患者的预后仍然很差。治疗选择有限,没有一个能够显示出生存益处。在一项随机试验中,伊匹木单抗是第一种在皮肤黑色素瘤患者中显示生存获益的药物。但是,有关其在高级UM管理中的作用的公开证据有限。在这里,我们报告了在英国一家学术癌症中心接受治疗的5例晚期UM患者的ipilimumab经验。两名患者患有持续稳定的疾病,三名患有进行性疾病。在病情稳定的患者中,一名患者在开始治疗后的11个月就保持了疾病控制,与基线相比肿瘤体积减少了约10%,第二名患者在15个月后进展。我们还检查了与皮肤黑色素瘤中的ipilimumab相似的肿瘤动力学和反应模式。由于缺乏随机试验数据,我们的研究结果表明,依匹莫单抗可能是晚期UM患者的合理治疗选择。

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