ENSAT registry-based randomized clinical trials for adrenocortical carcinoma

临床试验 随机对照试验 医学 肾上腺皮质癌 疾病 随机化 疾病登记处 重症监护医学 内科学
作者
Joakim Crona,Éric Baudin,Massimo Terzolo,Alexandra Chrisoulidou,Anna Angelousi,Cristina Rabascio,Cristina Lamas Oliveira,Els J. M. Nieveen van Dijkum,Filippo Ceccato,Françoise Borson‐Chazot,Giuseppe Reimondo,Guido A M Tiberi,Hester Ettaieb,Andreas Kiriakopoulos,Letizia Canu,Darko Kaštelan,Esthr Osher,Eugenia Yiannakopoulou,Giorgio Arnaldi,Guillaume Assié,Isabel Paiva,Isabelle Bourdeau,John Newell‐Price,Karolina M. Nowak,Mario Romero,Maria Cristina De Martino,Maria João Bugalho,Mark Sherlock,Marie-Christine Vantyghem,Michael Conall Dennedy,Paula Loli,Patrice Rodien,Richard A Feelders,Ronald R. de Krijger,Sam Van Slycke,Simon Aylwin,Valentina Morelli,Laurent Vroonen,Zulfiya Shafigullina,Irina Bancos,Małgorzata Trofimiuk–Müldner,Marcus Quinkler,Michaela Luconi,Matthias Kroiß,Mitsuhide Naruse,Péter Igaz,Radu Mihai,Silvia Della Casa,Alfredo Berruti,Martin Fassnacht,Felix Beuschlein
出处
期刊:European journal of endocrinology [Oxford University Press]
卷期号:184 (2): R51-R59 被引量:11
标识
DOI:10.1530/eje-20-0800
摘要

Adrenocortical carcinoma (ACC) is an orphan disease lacking effective systemic treatment options. The low incidence of the disease and high cost of clinical trials are major obstacles in the search for improved treatment strategies. As a novel approach, registry-based clinical trials have been introduced in clinical research, so allowing for significant cost reduction, but without compromising scientific benefit. Herein, we describe how the European Network for the Study of Adrenal Tumours (ENSAT) could transform its current registry into one fit for a clinical trial infrastructure. The rationale to perform randomized registry-based trials in ACC is outlined including an analysis of relevant limitations and challenges. We summarize a survey on this concept among ENSAT members who expressed a strong interest in the concept and rated its scientific potential as high. Legal aspects, including ethical approval of registry-based randomization were identified as potential obstacles. Finally, we describe three potential randomized registry-based clinical trials in an adjuvant setting and for advanced disease with a high potential to be executed within the framework of an advanced ENSAT registry. Thus we, therefore, provide the basis for future registry-based trials for ACC patients. This could ultimately provide proof-of-principle of how to perform more effective randomized trials for an orphan disease.

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