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From Clinical Trials to the Front Line: Vinflunine for Treatment of Urothelial Cell Carcinoma at the National Cancer Institute of Naples

机译:从临床试验到第一线:那不勒斯国家癌症研究所的长春氟宁治疗尿道上皮细胞癌

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Background: The efficacy of Vinflunine, after failure of platinum-based chemotherapy in patients with metastatic or recurrent Transitional Cell Cancer of the Urothelial Tract, TCCU, has been demonstrated in an international, randomized, phase III trial comparing Vinflunine plus Best Supportive Care, BSC, with BSC alone. On the basis of that study vinflunine has been approved by the European Medicine Association, EMA, for treatment of TCCU patients after failure of a platinum treatment. However, since data in clinical trials often differ from routine clinical practice due to unselected population and less strict monitoring, “real life” experiences are very helpful to verify the efficacy of a new therapy. Methods: This was a spontaneous, observational, retrospective study involving 43 patients with metastatic TCCU treated with vinflunine at our cancer center, data about demographics, disease characteristics, and previous treatments were collected and outcome and toxicities of vinflunine were analyzed. Results: 41 of 43 patients were eligible for RR analysis, the Overall RR was 12%, the Disease Control Rate was 29%; when including only patients treated in II line the DCR rose to 33%; the median PFS and the median OS were 2.2 and 6.9 months, respectively. Conclusion: Our findings were consistent with the outcome data emerged in the phase III randomized trial and in the other observational studies conducted all around Europe in the last 2–3 years. This experience supports the use of vinflunine in patients with advanced TTCU as effective and manageable antineoplastic drug.
机译:背景:一项国际性的,随机对照的,III期临床试验证明了长春氟宁对转移性或复发性尿道导管转移性细胞癌TCCU患者的疗效,该试验比较了长春氟宁与最佳支持治疗,仅使用BSC。在该研究的基础上,长春氟宁已被欧洲医学协会EMA批准用于铂类药物治疗失败后的TCCU患者的治疗。但是,由于人群选择不多且监测不严格,临床试验中的数据通常与常规临床实践有所不同,因此“现实生活”经验对于验证新疗法的有效性非常有帮助。方法:这是一项自发的观察性回顾性研究,研究对象为43名在我们癌症中心接受长春氟宁治疗的转移性TCCU患者,收集了有关人口统计学,疾病特征和以前治疗的数据,并分析了长春氟宁的疗效和毒性。结果:43例患者中有41例符合RR分析,总RR为12%,疾病控制率为29%;当仅包括接受II线治疗的患者时,DCR上升至33%; PFS和OS的中位数分别为2.2个月和6.9个月。结论:我们的发现与过去2-3年中在整个欧洲进行的III期随机试验和其他观察性研究中得出的结果数据一致。这项经验支持在长时TTCU患者中使用长春氟宁作为有效且可控的抗肿瘤药。

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