医学
置信区间
内科学
优先次序
肿瘤科
前瞻性队列研究
癌症
医学诊断
重症监护医学
儿科
病理
经济
管理科学
作者
Cornelis M. van Tilburg,Elke Pfaff,Kristian W. Pajtler,Karin P.S. Langenberg,Petra Fiesel,Barbara C. Jones,Gnana Prakash Balasubramanian,Sebastian Stark,Pascal D. Johann,Mirjam Blattner-Johnson,Kathrin Schramm,Nicola Dikow,Steffen Hirsch,Christian Sutter,Kerstin Grund,Arend von Stackelberg,Andreas E. Kulozik,Andrej Lissat,Arndt Borkhardt,Roland Meisel
出处
期刊:Cancer Discovery
[American Association for Cancer Research]
日期:2021-08-09
卷期号:11 (11): 2764-2779
被引量:196
标识
DOI:10.1158/2159-8290.cd-21-0094
摘要
Abstract INFORM is a prospective, multinational registry gathering clinical and molecular data of relapsed, progressive, or high-risk pediatric patients with cancer. This report describes long-term follow-up of 519 patients in whom molecular alterations were evaluated according to a predefined seven-scale target prioritization algorithm. Mean turnaround time from sample receipt to report was 25.4 days. The highest target priority level was observed in 42 patients (8.1%). Of these, 20 patients received matched targeted treatment with a median progression-free survival of 204 days [95% confidence interval (CI), 99–not applicable], compared with 117 days (95% CI, 106–143; P = 0.011) in all other patients. The respective molecular targets were shown to be predictive for matched treatment response and not prognostic surrogates for improved outcome. Hereditary cancer predisposition syndromes were identified in 7.5% of patients, half of which were newly identified through the study. Integrated molecular analyses resulted in a change or refinement of diagnoses in 8.2% of cases. Significance: The pediatric precision oncology INFORM registry prospectively tested a target prioritization algorithm in a real-world, multinational setting and identified subgroups of patients benefiting from matched targeted treatment with improved progression-free survival, refinement of diagnosis, and identification of hereditary cancer predisposition syndromes. See related commentary by Eggermont et al., p. 2677 . This article is highlighted in the In This Issue feature, p. 2659
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