The pediatric precision oncology inform registry: Clinical outcome and benefit for patients with very high-evidence targets

  • Cornelis M. Van Tilburg (Corresponding Author)
  • , Elke Pfaff
  • , Kristian W. Pajtler
  • , Karin P.S. Langenberg
  • , Petra Fiesel
  • , Barbara C. Jones
  • , Gnana Prakash Balasubramanian
  • , Sebastian Stark
  • , Pascal D. Johann
  • , Mirjam Eleonora Blattner-Johnson
  • , Kathrin Schramm
  • , Nicola Dikow
  • , Steffen Hirsch
  • , Christian Sutter
  • , Kerstin Grund
  • , Arend Von Stackelberg
  • , Andreas E. Kulozik
  • , Andrej Lissat
  • , Arndt Borkhardt
  • , Roland Meisel
  • Dirk Reinhardt, Jan Henning Klusmann, Gudrun Fleischhack, Stephan Tippelt, Dietrich Von Schweinitz, Irene Schmid, Christof M. Kramm, André O. Von Bueren, Gabriele Calaminus, Peter Vorwerk, Norbert Graf, Frank Westermann, Matthias Fischer, Angelika Eggert, Birgit Burkhardt, Wilhelm Wößmann, Michaela Nathrath, Stefanie Hecker-Nolting, Michael C. Frühwald, Dominik T. Schneider, Ines B. Brecht, Petra Ketteler, Simone Fulda, Ewa Koscielniak, Michael T. Meister, Monika Scheer, Simone Hettmer, Matthias Schwab, Roman Tremmel, Ingrid Øra, Caroline Hutter, Nicolas U. Gerber, Olli Lohi, Bernarda Kazanowska, Antonis Kattamis, Maria Filippidou, Bianca Goemans, C. Michel Zwaan, Till Milde, Natalie Jäger, Stephan Wolf, David Reuss, Felix Sahm, Andreas Von Deimling, Uta Dirksen, Angelika Freitag, Ruth Witt, Peter Lichter, Annette Kopp-Schneider, David T.W. Jones, Jan J. Molenaar, David Capper, Stefan M. Pfister, Olaf Witt

Research output: Contribution to journalArticlepeer-review

196 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)2764-2779
Number of pages16
JournalCancer Discovery
Volume11
Issue number11
DOIs
Publication statusPublished - Nov 2021
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Field of Science*

  • 3.2 Clinical medicine
  • 3.1 Basic medicine

Publication Type*

  • 1.1. Scientific article indexed in Web of Science and/or Scopus database

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