...
首页> 外文期刊>British Journal of Dermatology >A randomized, multinational, noninferiority, phase III III trial to evaluate the safety and efficacy of BF BF ‐200 aminolaevulinic acid gel vs. methyl aminolaevulinate cream in the treatment of nonaggressive basal cell carcinoma with photodynamic therapy
【24h】

A randomized, multinational, noninferiority, phase III III trial to evaluate the safety and efficacy of BF BF ‐200 aminolaevulinic acid gel vs. methyl aminolaevulinate cream in the treatment of nonaggressive basal cell carcinoma with photodynamic therapy

机译:随机,跨国,非事实体,第III期III III期试验,以评估BF BF -200氨基乙酰乙酰胆酸凝胶与甲基氨基乙酰乙烯基乳膏的安全性和功效治疗具有光动力学疗法的非收力基础细胞癌

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Summary Background Basal cell carcinoma ( BCC ) represents the most common nonmelanoma skin cancer worldwide, affecting mainly adult, fair‐skinned individuals. The World Health Organization distinguishes aggressive and nonaggressive forms, of which prototypical variants of the latter are primary nodular and superficial BCC . Objectives To demonstrate noninferiority of BF ‐200 ALA (a nanoemulsion gel containing 5‐aminolaevulinic acid) compared with MAL (a cream containing methyl aminolaevulinate) in the treatment of nonaggressive BCC with photodynamic therapy ( PDT ). Noninferiority of the primary efficacy variable (overall patient complete response 12 weeks after last PDT ) would be declared if the mean response for BF ‐200 ALA was no worse than that for MAL , within a statistical margin of Δ = ?15%. Methods The study was a randomized, phase III trial performed in Germany and the U.K. with ongoing 5‐year follow‐up. Of 281 randomized patients, 138 were treated with BF ‐200 ALA and 143 with MAL . Patients received two PDT sessions 1 week apart. Remaining lesions 12 weeks after the second PDT were retreated. Illumination was performed with a red light source (635 nm, 37 J cm ?2 ). The results shown include clinical end points and patients’ reassessment 12 months after the last PDT . The study was registered with Eudra CT (number 2013‐003241‐42). Results Of the BF ‐200 ALA ‐treated patients, 93·4% were complete responders compared with 91·8% in the MAL group. The difference of means was 1·6, with a one‐sided 97·5% confidence interval of ?6·5, establishing noninferiority ( P 0·0001). The results for secondary efficacy parameters were in line with the primary outcome. Recurrence rates 12 months after the last treatment were ≤ 10%. Conclusions Treatment of nonaggressive BCC with BF ‐200 ALA ‐ PDT is highly effective and well tolerated with proven noninferiority to MAL ‐ PDT . It demonstrates low recurrence rates after 1 year of follow‐up.
机译:发明内容背景基础细胞癌(BCC)代表全球最常见的非梅兰肿瘤癌,主要影响成人,公平皮肤的个体。世界卫生组织区分了侵略性和非侵略性形式,其中后者的原型变体是初级结节性和肤浅的BCC。与MAL(含甲基氨基乙酰乙酰丁酸盐)的MAR(含甲基氨基纤维酸)的含有5-氨基乙酰丙酸的纳米乳剂凝胶的含义的目标证明非易失异的目的,用于治疗具有光动力学治疗(PDT)的非收力BCC。如果BF -200 ALA的平均反应没有比MAL的平均响应在Δ= 15%的统计边缘内,则将宣布初级疗效变量的非疗效变量(最后的PDT后12周的整体患者的响应)将被宣布。方法该研究是在德国和U.K的随机,第III次审判中进行,随着5年的跟进。在281例随机患者中,138例用BF -200 ALA和143处理,用MAL处理。患者接受了一周的两个PDT会话。第二次PDT后12周后剩余病变。用红色光源(635nm,37J厘米2)进行照明。结果显示的结果包括最后一次PDT后12个月的临床目的和患者重新评估。该研究在EUDRA CT(2013-003241-42号)注册。 BF -200 Ala -.Treated患者的结果,93·4%是完全响应者,而MAL组的91·8%相比。平均值的差异为1·6,具有单侧的97·5%置信区间的α6·5,建立非闭合性(P <0·0001)。二次疗效参数的结果与主要结果一致。最后一次治疗后12个月的复发率≤10%。结论与BF -200 ALA - PDT的非侵略性BCC的处理高效且耐受性耐受性的非侵入性对MAL - PDT。随访后,它展示了低复发率。

著录项

  • 来源
    《British Journal of Dermatology》 |2018年第2期|共11页
  • 作者单位

    Dermatology DepartmentStirling Community HospitalStirling U.K.;

    ProDermaDülmen Germany;

    Private Dermatological PracticeFriedrichshafen Germany;

    CentroDerm GmbH Wuppertal and Faculty of HealthUniversity Witten/HerdeckeWitten Germany;

    Dermatologikum Kiel and Department of DermatologyUniversity Hospital Schleswig‐Holstein (UKSH)Kiel;

    Medical Centre BonnBonn Germany;

    Department of DermatologyUniversity Hospital Carl Gustav CarusDresden Germany;

    CMB Collegium Medicum Berlin GmbHBerlin Germany;

    St Mary's HospitalPortsmouth U.K.;

    MENSINGDERMA research GmbHHamburg Germany;

    Photobiology UnitUniversity of DundeeDundee U.K.;

    ZENTdermaM?nchengladbach Germany;

    Department of Dermatology and AllergologyUniversity Hospital MunichMunich Germany;

    Dermatological Private PracticeClinical Research and Laser MedicineBerlin Germany;

    Specialist Hospital HornheideDepartment of DermatologyMünster Germany;

    Dermatology and Allergology Practice at the Clinical Centre HanauHanau Germany;

    Centre for Dermatology VechtaVechta Germany;

    Private PracticeFreising Germany;

    Private PracticeMahlow Germany;

    Department of DermatologyClinical Centre Lippe GmbH DetmoldDetmold Germany;

    Department of DermatologyUniversity Hospital Johannes Gutenberg University MainzMainz Germany;

    Monklands HospitalGlasgow U.K.;

    Private PracticeWuppertal Germany;

    Clinipace – Accovion GmbHEschborn Germany;

    Biofrontera Bioscience GmbHLeverkusen Germany;

    Biofrontera Bioscience GmbHLeverkusen Germany;

    Biofrontera Bioscience GmbHLeverkusen Germany;

    Department of Dermatology and AllergologyVest ClinicRecklinghausen Germany;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 皮肤病学与性病学;
  • 关键词

相似文献

  • 外文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号