Implementation of paediatric precision oncology into clinical practice: The Individualized Therapies for Children with cancer program ‘iTHER’

Karin P.S. Langenberg(Princess Máxima Center), Michael T. Meister(Oncode Institute), Jette J. Bakhuizen(Heidelberg University), Judith M. Boer(Princess Máxima Center), Natasha K. A. van Eijkelenburg(Princess Máxima Center), Esther Hulleman(Princess Máxima Center), Uri Ilan(Princess Máxima Center), Eleonora J. Looze(Princess Máxima Center), Miranda P. Dierselhuis(Princess Máxima Center), Jasper van der Lugt(Princess Máxima Center), Willemijn B. Breunis(Princess Máxima Center), Linda Schild(Princess Máxima Center), Kimberley Ober(Princess Máxima Center), Sander R. van Hooff(Princess Máxima Center), Marijn A. Scheijde‐Vermeulen(Heidelberg University), Laura S. Hiemcke‐Jiwa(Heidelberg University), Uta Flucke(Heidelberg University), Mariëtte E.G. Kranendonk(Heidelberg University), Pieter Wesseling(Heidelberg University), Edwin Sonneveld(Princess Máxima Center), Simone Punt(Heidelberg University), Arjan Boltjes(Princess Máxima Center), Freerk van Dijk(Princess Máxima Center), Eugène T.P. Verwiel(Princess Máxima Center), Richard Volckmann(Amsterdam University Medical Centers), Jayne Y. Hehir‐Kwa(Princess Máxima Center), Lennart Kester(Princess Máxima Center), Marco M.J. Koudijs(Heidelberg University), Esmé Waanders(Heidelberg University), Frank C. P. Holstege(Heidelberg University), Josef Vormoor(Princess Máxima Center), Eelco W. Hoving(Princess Máxima Center), Max M. van Noesel(Heidelberg University), Rob Pieters(Princess Máxima Center), Marcel Kool(German Cancer Research Center), Miriam Stumpf(Princess Máxima Center), Mirjam Blattner-Johnson(German Cancer Research Center), Gnana Prakash Balasubramanian(German Cancer Research Center), Cornelis M. van Tilburg(German Cancer Research Center), Barbara C. Jones(German Cancer Research Center), David Jones(German Cancer Research Center), Olaf Witt(German Cancer Research Center), Stefan M. Pfister(German Cancer Research Center), Marjolijn C.J. Jongmans(Heidelberg University), Roland P. Kuiper(Heidelberg University), Ronald R. de Krijger(Heidelberg University), Marc H W Wijnen(Princess Máxima Center), Monique L. den Boer(Princess Máxima Center), C. Michel Zwaan(Princess Máxima Center), Patrick Kemmeren(Heidelberg University), Jan Köster(Amsterdam University Medical Centers), Bastiaan B.J. Tops(Princess Máxima Center), Bianca F. Goemans(Princess Máxima Center), Jan J. Molenaar(Utrecht University)
European Journal of Cancer
September 28, 2022
Cited by 58Open Access
Full Text

Abstract

iTHER is a Dutch prospective national precision oncology program aiming to define tumour molecular profiles in children and adolescents with primary very high-risk, relapsed, or refractory paediatric tumours. Between April 2017 and April 2021, 302 samples from 253 patients were included. Comprehensive molecular profiling including low-coverage whole genome sequencing (lcWGS), whole exome sequencing (WES), RNA sequencing (RNA-seq), Affymetrix, and/or 850k methylation profiling was successfully performed for 226 samples with at least 20% tumour content. Germline pathogenic variants were identified in 16% of patients (35/219), of which 22 variants were judged causative for a cancer predisposition syndrome. At least one somatic alteration was detected in 204 (90.3%), and 185 (81.9%) were considered druggable, with clinical priority very high (6.1%), high (21.3%), moderate (26.0%), intermediate (36.1%), and borderline (10.5%) priority. iTHER led to revision or refinement of diagnosis in 8 patients (3.5%). Temporal heterogeneity was observed in paired samples of 15 patients, indicating the value of sequential analyses. Of 137 patients with follow-up beyond twelve months, 21 molecularly matched treatments were applied in 19 patients (13.9%), with clinical benefit in few. Most relevant barriers to not applying targeted therapies included poor performance status, as well as limited access to drugs within clinical trial. iTHER demonstrates the feasibility of comprehensive molecular profiling across all ages, tumour types and stages in paediatric cancers, informing of diagnostic, prognostic, and targetable alterations as well as reportable germline variants. Therefore, WES and RNA-seq is nowadays standard clinical care at the Princess Máxima Center for all children with cancer, including patients at primary diagnosis. Improved access to innovative treatments within biology-driven combination trials is required to ultimately improve survival.


Related Papers

No related papers found

Powered by citation graph analysis