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首页> 外文期刊>BMC Cancer >Phase II trial to investigate the safety and efficacy of orally applied niclosamide in patients with metachronous or sychronous metastases of a colorectal cancer progressing after therapy: the NIKOLO trial
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Phase II trial to investigate the safety and efficacy of orally applied niclosamide in patients with metachronous or sychronous metastases of a colorectal cancer progressing after therapy: the NIKOLO trial

机译:II期临床试验旨在探讨口服尼古拉胺对结直肠癌异位或异位转移患者在治疗后进展的安全性和有效性:NIKOLO试验

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Colorectal cancer (CRC) is the second most common cause of all cancer deaths in Europe and the Western world with a lifetime risk of approximately 5%. Despite several improvements in the treatment of patients with unresectable CRC prognosis is poor and there is the need of developing new treatment strategies for patients with metastatic chemorefractory disease. The S100 calcium binding protein A4 (S100A4) predicts metastasis formation and reduced CRC patient survival. S100A4 was previously identified as transcriptional target of the Wnt/β-catenin signaling pathway. The Food and Drug Administration (FDA)-approved anti-helminthic drug niclosamide is known to intervene in the Wnt/β-catenin pathway signaling, leading to reduced expression of S100A4 linked to restricted in vivo metastasis formation. Thus, we aim at translation of our findings on restricting S100A4-driven metastasis into clinical practice for treating metastasized CRC patients progressing after standard therapy. NIKOLO is a phase II, single center, one-arm open-label clinical trial to investigate the safety and efficacy of niclosamide tablets in patients with metastasized CRC progressing under standard therapy. Eligible patients will receive 2?g of orally applied niclosamide once a day and will continue with the treatment once daily till disease progression or toxicity. Toxicities will be graded according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v4.03. The primary objective of this trial is to assess the progression free survival after 4?months, secondary objectives are overall survival, time to progression, disease control rate (remission + partial remission + stable disease), and safety. Furthermore, pharmacokinetic analysis will be conducted to evaluate niclosamide plasma concentration. This study is expected to provide evidence of the feasibility, toxicity and efficacy of niclosamide in the treatment of patients with metastasized CRC and could help to establish a new treatment option. The study is registered with ClinicalTrials.gov ( NCT02519582 ) and the European Clinical Trials Database (EudraCT 2014-005151-20).
机译:大肠癌(CRC)是欧洲和西方世界所有癌症死亡的第二大最常见原因,终生风险约为5%。尽管在无法切除的CRC患者的治疗方面取得了一些进步,但对于转移性化学难治性疾病患者,仍需要开发新的治疗策略。 S100钙结合蛋白A4(S100A4)预测转移形成并降低CRC患者的生存率。 S100A4先前被确定为Wnt /β-catenin信号通路的转录靶标。已知已获得美国食品药品监督管理局(FDA)批准的抗蠕虫药niclosamide干预Wnt /β-catenin信号通路,导致S100A4的表达减少,这与体内转移形成受到限制有关。因此,我们旨在将我们的发现限制在将S100A4驱动的转移限制为临床实践,以治疗标准疗法后进展的转移性CRC患者。 NIKOLO是一项II期,单中心,单臂开放标签临床试验,旨在研究烟酰胺片在标准治疗下对转移性CRC进展的患者的安全性和有效性。符合条件的患者每天口服2微克尼洛酰胺,并将继续每天治疗一次,直至疾病进展或出现毒性。毒性将根据美国国家癌症研究所不良事件通用术语标准(NCI CTCAE)v4.03进行分级。该试验的主要目的是评估4个月后的无进展生存期,次要目标是总体生存期,进展时间,疾病控制率(缓解+部分缓解+疾病稳定)和安全性。此外,将进行药代动力学分析以评估烟酰胺的血浆浓度。该研究有望为尼洛沙胺治疗转移性CRC患者的可行性,毒性和疗效提供证据,并有助于建立新的治疗选择。该研究已在ClinicalTrials.gov(NCT02519582)和欧洲临床试验数据库(EudraCT 2014-005151-20)中注册。

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