Back to Search Start Over

The Pediatric Precision Oncology INFORM Registry: Clinical Outcome and Benefit for Patients with Very High-Evidence Targets

Authors :
van Tilburg, Cornelis M.
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
von Schweinitz, Dietrich
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.
Witt, Olaf
van Tilburg, Cornelis M.
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
von Schweinitz, Dietrich
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.
Witt, Olaf
Publication Year :
2021

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.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1312208237
Document Type :
Electronic Resource