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Tilburg, Cornelis M. van; Pfaff, Elke; Pajtler, Kristian W.; Langenberg, Karin P. S.; Fiesel, Petra; Jones, Barbara C.; Balasubramanian, Gnana Prakash; Stark, Sebastian; Johann, Pascal D.; Blattner-Johnson, Mirjam; Schramm, Kathrin; Dikow, Nicola; Hirsch, Steffen; Sutter, Christian; Grund, Kerstin; von Stackelberg, Arend; Kulozik, Andreas E.; Lissat, Andrej; Borkhardt, Arndt; Meisel, Roland; Reinhardt, Dirk; Klusmann, Jan-Henning; Fleischhack, Gudrun; Tippelt, Stephan; Schweinitz, Dietrich von; Schmid, Irene; Kramm, Christof M.; von Bueren, Andre O.; Calaminus, Gabriele; Vorwerk, Peter; Graf, Norbert; Westermann, Frank; Fischer, Matthias; Eggert, Angelika; Burkhardt, Birgit; Woessmann, Wilhelm; Nathrath, Michaela; Hecker-Nolting, Stefanie; Fruehwald, Michael C.; Schneider, Dominik T.; Brecht, Ines B.; Ketteler, Petra; Fulda, Simone; Koscielniak, Ewa; Meister, Michael T.; Scheer, Monika; Hettmer, Simone; Schwab, Matthias; Tremmel, Roman; Ora, Ingrid; Hutter, Caroline; Gerber, Nicolas U.; Lohi, Olli; Kazanowska, Bernarda; Kattamis, Antonis; Filippidou, Maria; Goemans, Bianca; Zwaan, C. Michel; Milde, Till; Jaeger, Natalie; Wolf, Stephan; Reuss, David; Sahm, Felix; von Deimling, Andreas; Dirksen, Uta; Freitag, Angelika; Witt, Ruth; Lichter, Peter; Kopp-Schneider, Annette; Jones, David T. W.; Molenaar, Jan J.; Capper, David; Pfister, Stefan M. and Witt, Olaf (2021): The Pediatric Precision Oncology INFORM Registry: Clinical Outcome and Benefit for Patients with Very High-Evidence Targets. In: Cancer Discovery, Vol. 11, No. 11: pp. 2764-2779

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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.

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