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首页> 外文期刊>Trials >CApecitabine plus Radium-223 (Xofigo?) in breast cancer patients with BONe metastases (CARBON): study protocol for a phase IB/IIA randomised controlled trial
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CApecitabine plus Radium-223 (Xofigo?) in breast cancer patients with BONe metastases (CARBON): study protocol for a phase IB/IIA randomised controlled trial

机译:Capecitabine Plus乳腺癌患者乳腺癌患者(碳):IA型IIA的研究方案,用于乳腺转移患者(碳):IA型随机对照试验

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BACKGROUND:A substantial proportion of breast cancer patients develop metastatic disease, with over 450,000 deaths globally per year. Bone is the most common first site of metastatic disease accounting for 40% of all first recurrence and 70% of patients with advanced disease develop skeletal involvement. Treatment of bone metastases currently focusses on symptom relief and prevention and treatment of skeletal complications. However, there remains a need for further treatment options for patients with bone metastases. Combining systemic therapy with a bone-targeted agent, such as radium-223, may provide an effective treatment with minimal additional side effects.METHODS/DESIGN:CARBON is a UK-based, open-label, multi-centre study which comprises an initial safety phase to establish the feasibility and safety of combining radium-223 given on a 6-weekly schedule in combination with orally administered capecitabine followed by a randomised extension phase to further characterise the safety profile and provide preliminary estimation of efficacy.DISCUSSION:The CARBON study is important as the results will be the first to assess radium-223 with chemotherapy in advanced breast cancer. If the results find acceptable rates of toxicity with a decrease in bone turnover markers, further work will be necessary in a phase II/III setting to assess the efficacy and clinical benefit.TRIAL REGISTRATION:ISRCTN, ISRCTN92755158, Registered on 17 February 2016.
机译:背景:大量比例的乳腺癌患者发育转移性疾病,每年全球超过450,000人死亡。骨是最常见的第一个转移性疾病部位占所有第一复发的40%,70%的晚期疾病患者发挥骨骼受累。骨转移治疗目前侧重于症状浮雕和预防和治疗骨骼并发症。然而,仍然需要对骨转移患者进行进一步的治疗选择。将全身疗法与底棒 - 223等骨靶向剂相结合,可以提供有效的处理,其额外的副作用最小。方法/设计:碳是一种基于英国的开放式的多中心研究,包括初始安全阶段,建立与口服延伸阶段的603次安排组合给出的radium-223的可行性和安全性,然后进行随机伸展阶段,以进一步表征安全性,并提供效率的初步估计。探讨:碳研究重要的是,结果将成为第一个评估高乳腺癌的镭-223中的化疗。如果结果发现骨质周转标记减少的可接受的毒性税率,在II / III期的情况下,将进一步的工作是评估疗效和临床利益.Tial注册:ISRCTN,ISRCTN92755158,于2016年2月17日注册。

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