医学
四分位间距
内科学
肿瘤科
液体活检
靶向治疗
中期分析
耐火材料(行星科学)
临床终点
临床试验
癌症
物理
天体生物学
作者
Jakob M. Riedl,Samantha O. Hasenleithner,Gudrun Pregartner,Lukas Scheipner,Florian Posch,Karin Groller,Karl Kashofer,Stephan Jahn,Thomas Bauernhofer,Martin Pichler,Herbert Stöger,Andrea Berghold,Gerald Höefler,Michael R. Speicher,Ellen Heitzer,Armin Gerger
标识
DOI:10.1177/1758835920987658
摘要
BACKGROUND: Molecular profiling (MP) represents an opportunity to match patients to a targeted therapy and when tumor tissue is unavailable, circulating tumor deoxyribonucleic acid (ctDNA) can be harnessed as a non-invasive analyte for this purpose. We evaluated the success of a targeted therapy selected by profiling of ctDNA and tissue in patients with advanced and refractory carcinoma. PATIENTS AND METHODS: the CureMatch PreciGENE™ decision support algorithm. RESULTS: Interim analysis of 24 patients yielded informative results from 20 patients (83%). A potential tumor-specific drug could be matched in 11 patients (46%) and eight (33%) received a matched treatment. Median PFS in the matched treatment group was 61.5 days [interquartile range (IQR) 49.8-71.0] compared with 81.5 days (IQR 68.5-117.8) for the last evidence-based treatment, resulting in a median PFS ratio of 0.7 (IQR 0.6-0.9). Hence, as no patient experienced a PFS ratio ⩾1.2, the study was terminated. Except for one case, the CureMatch analysis identified either a two-drug or three-drug combination option. CONCLUSIONS: EudraCT: 2014-005341-44.
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