首页> 外文期刊>European journal of cancer: official journal for European Organization for Research and Treatment of Cancer (EORTC) [and] European Association for Cancer Research (EACR) >Multicentric parallel phase II trial of the polo-like kinase 1 inhibitor BI 2536 in patients with advanced head and neck cancer, breast cancer, ovarian cancer, soft tissue sarcoma and melanoma. The first protocol of the European Organization for Research and Treatment of Cancer (EORTC) Network Of Core Institutes (NOCI).
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Multicentric parallel phase II trial of the polo-like kinase 1 inhibitor BI 2536 in patients with advanced head and neck cancer, breast cancer, ovarian cancer, soft tissue sarcoma and melanoma. The first protocol of the European Organization for Research and Treatment of Cancer (EORTC) Network Of Core Institutes (NOCI).

机译:polo样激酶1抑制剂BI 2536在晚期头颈癌,乳腺癌,卵巢癌,软组织肉瘤和黑色素瘤患者中的多中心平行II期试验。欧洲癌症研究与治疗组织(EORTC)核心研究所网络(NOCI)的第一个协议。

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AIMS: BI 2536 is a selective and potent small-molecule inhibitor of polo-like kinase 1. We performed a multi-centre, multi-tumour phase II trial to investigate the efficacy, safety and pharmacokinetics of BI 2536 in five solid tumour types. PATIENTS AND METHODS: Patients with advanced head and neck, breast and ovarian cancer, soft tissue sarcoma and melanoma were selected according to protocol-defined general and tumour-specific criteria. They were 18years old, had a good performance status, adequate bone marrow, renal and liver function, measurable progressive disease and had completed other relevant systemic treatments >4weeks ago. BI 2536 200-250mg was given intravenously on day 1 every 3 weeks until intolerance, progression or refusal. The study was based on a Simon two-stage design, with 12 patients entering in stage 1 and additional 25 patients to be entered in case of at least one response in the first stage. The rate of objective responses (RECIST criteria) was chosen as primary end-point. RESULTS: Seventy six patients were included, 71 started treatment and received a median number of two cycles (four in ovarian cancer). Frequent grade 3-4 adverse events were neutropaenia (81.6%), thrombocytopaenia (19.7%), febrile neutropaenia (19.7%), anaemia (15.5%) and pain (9.9%). We did not observe confirmed objective responses. All cohorts were closed after the entry of 14-15 eligible non-responding patients. Pharmacokinetic analyses revealed multi-compartmental behaviour and a rapid distribution of BI 2536. CONCLUSIONS: BI 2536 showed limited antitumour activity according to the design of this trial in five different tumour types. Derivatives of BI 2536 with a more favourable pharmacological profile are currently explored further in prospective studies.
机译:目的:BI 2536是polo样激酶1的选择性强效小分子抑制剂。我们进行了一项多中心,多肿瘤II期临床试验,以研究BI 2536在五种实体瘤类型中的功效,安全性和药代动力学。患者和方法:根据方案定义的一般和肿瘤特异性标准,选择患有晚期头颈癌,乳腺癌和卵巢癌,软组织肉瘤和黑色素瘤的患者。他们今年18岁,身体状况良好,骨髓,肾和肝功能良好,可测量的进行性疾病,并且在4周前完成了其他相关的全身治疗。第1天每3周静脉给予BI 2536 200-250mg,直到出现不耐受,进展或拒绝。该研究基于西蒙的两阶段设计,第一阶段有12名患者进入研究,而在第一阶段至少有一种反应的情况下,将有25名患者进入研究。选择客观反应率(RECIST标准)作为主要终点。结果:共纳入76例患者,其中71例开始接受治疗,平均接受了两个周期的治疗(卵巢癌为四个周期)。常见的3-4级不良事件为中性粒细胞减少症(81.6%),血小板减少症(19.7%),高热性中性粒细胞减少症(19.7%),贫血(15.5%)和疼痛(9.9%)。我们没有观察到证实的客观反应。入组14-15名无反应的患者后,所有队列均关闭。药代动力学分析表明,BI 2536具有多室行为,并且分布迅速。结论:根据该试验的设计,BI 2536在五种不同的肿瘤类型中显示出有限的抗肿瘤活性。目前在前瞻性研究中进一步探索了具有更有利药理学特征的BI 2536衍生物。

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