Recommendations for the collection and annotation of biosamples for analysis of biomarkers in neurofibromatosis and schwannomatosis clinical trials

Author:

Sundby R Taylor1ORCID,Rhodes Steven D2,Komlodi-Pasztor Edina3,Sarnoff Herb45,Grasso Vito67,Upadhyaya Meena8,Kim AeRang9,Evans D Gareth10,Blakeley Jaishri O11,Hanemann C Oliver12,Bettegowda Chetan13

Affiliation:

1. Pediatric Oncology Branch, National Cancer Institute, Bethesda, MD, USA

2. Division of Hematology/Oncology/Stem Cell Transplant, Department of Pediatrics, Herman B Wells Center for Pediatric Research, School of Medicine, Indiana University, Indianapolis, IN, USA

3. Department of Neurology, MedStar Georgetown University Hospital, Washington, DC, USA

4. Research and Development, Infixion Bioscience, Inc., San Diego, CA, USA

5. Patient Representative, REiNS International Collaboration, San Diego, CA, USA

6. Neural Stem Cell Institute, Rensselaer, NY, USA

7. Patient Representative, REiNS International Collaboration, Troy, NY, USA

8. Division of Cancer and Genetics, Cardiff University, Wales, UK

9. Center for Cancer and Blood Disorders, Children’s National Hospital, Washington, DC, USA

10. Manchester Centre for Genomic Medicine, St Mary’s Hospital, Manchester Academic Health Sciences Centre (MAHSC), ERN GENTURIS, Division of Evolution, Infection and Genomics, The University of Manchester, Manchester, UK

11. Division of Neuro-Oncology, Department of Neurology, School of Medicine, Johns Hopkins University, Baltimore, MD, USA

12. Peninsula Medical School, University of Plymouth, Plymouth, UK

13. Department of Neurosurgery, School of Medicine, Johns Hopkins University, Baltimore, MD, USA

Abstract

Introduction Neurofibromatosis 1 and schwannomatosis are characterized by potential lifelong morbidity and life-threatening complications. To date, however, diagnostic and predictive biomarkers are an unmet need in this patient population. The inclusion of biomarker discovery correlatives in neurofibromatosis 1/schwannomatosis clinical trials enables study of low-incidence disease. The implementation of a common data model would further enhance biomarker discovery by enabling effective concatenation of data from multiple studies. Methods The Response Evaluation in Neurofibromatosis and Schwannomatosis biomarker working group reviewed published data on emerging trends in neurofibromatosis 1 and schwannomatosis biomarker research and developed recommendations in a series of consensus meetings. Results Liquid biopsy has emerged as a promising assay for neurofibromatosis 1/schwannomatosis biomarker discovery and validation. In addition, we review recommendations for a range of biomarkers in clinical trials, neurofibromatosis 1/schwannomatosis–specific data annotations, and common data models for data integration. Conclusion These Response Evaluation in Neurofibromatosis and Schwannomatosis consensus guidelines are intended to provide best practices for the inclusion of biomarker studies in neurofibromatosis 1/schwannomatosis clinical trials, data, and sample annotation and to lay a framework for data harmonization and concatenation between trials.

Publisher

SAGE Publications

Subject

Pharmacology,General Medicine

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