Companion and Complementary Diagnostics From Biomarker Discovery to Clinical Implementation
Coordonnateur : Jørgensen Jan Trøst
Companion and Complementary Diagnostics: From Biomarker Discovery to Clinical Implementation provides readers with in-depth insights into the individual steps in the development of companion diagnostic assays, from the early biomarker discovery phase straight through to final regulatory approval. Further, the clinical implementation of companion diagnostic testing in the clinic is also discussed. As the development of predictive or selective biomarker assays linked to specific drugs is substantially increasing, this book offers comprehensive information on this quickly-evolving area of biomedicine. It is an essential resource for those in academic institutions, hospitals and pharma, and biotech and diagnostic commercial companies.
1. Foreword 2. An Introduction to Companion and Complementary Diagnostics 3. The Drug-Diagnostic Co-Development Model 4. Systems Biology and Biomarker Development in Cancer Signaling Therapy 5. Immunohistochemistry 6. In Situ Hybridization 7. Polymerase Chain Reaction 8. Next Gen Sequencing Based Companion Diagnostics: From Biomarker Discovery to Clinical Implementation 9. Current Next Generation Sequencing Based Companion Diagnostics and their Analytical Validation 10. Companion and Complementary Diagnostics by Mass Spectrometry 11. Molecular Imaging Companion Diagnostics 12. Circulating Tumor DNA Analysis and Opportunities for Personalized Cancer Medicine 13. Companion Diagnostics Assay Development – Prototype, Verification and Analytical Validation 14. Tissue is the Issue: Challenges in Oncology Clinical Trial Tissue Sample Collection for Biomarker Analyses and Companion Diagnostics 15. Adaptive Trial Designs for Biomarker Driven Clinical Trials with Quantitative and Multiple Candidate Biomarkers 16. Companion Diagnostics Based on Time to Event Data 17. Regulatory Requirements for Companion Diagnostics and Drug-Diagnostic Co-Development in the United States of America 18. Companion Diagnostics and Biomarker Tests in the European Medicines Agency’s Assessment of Medicinal Products 19. Understanding the Current Regulatory Landscape for Companion Diagnostic Products in China 20. Regulatory requirements for companion diagnostics – Japan 21. Economic Evaluation of Companion and Complementary Diagnostics 22. A Risk Based Paradigm of Biomarkers in Clinical Trials 23. Implementing Companion Diagnostic Testing in the Clinic 24. Osimertinib (TAGRISSO) and the cobas EGFR Mutation Test v2 25. QMS Omecamtiv Mecarbil Immunoassay and Omecamtiv Mecarbil Co-Development 26. Current Status and Future Direction of Companion Diagnostics
Scientists and health care professionals working in academic research institutions, hospitals as well as pharma, biotech and diagnostic companies. Also academics in molecular biologist, human biologists, clinical chemists, bio-engineers, biostatisticians /bioinformatics, pharmacists, pathologists, and clinicians.
- Covers all aspects, from biomarker discovery, to development and regulatory approval
- Explains the "how to" aspects of companion diagnostics
- Incorporates information on the entire process, allowing for easier and deeper understanding of the topic
Date de parution : 05-2019
Ouvrage de 508 p.
19x23.3 cm
Thèmes de Companion and Complementary Diagnostics :
Mots-clés :
18F-fluorodeoxyglucose; ALK; ALK (anaplastic lymphoma kinase); Adaptive designs; Adaptive enrichment; Analytical validation; And Welfare; Anticancer drugs; Assay development; Assay validation; Biomarker; Biomarker cut point; Biomarkers; Bootstrap resampling; Breakpoint; Breast; Bridging studies; CDx; CE-Mark; Cancer; Center for Medical Device Evaluation (CMDE); Certification; China National Drug Administration (CNDA); Circulating tumor DNA; Clinical evidence; Clinical laboratory diagnoses; Clinical trial; Clinical trials; Clinical utility; Clinical validation; Clonal evolution; Cobas EGFR Mutation Test v2; Codevelopment; Companion diagnostic; Companion diagnostic (CDx); Companion diagnostics; Complementary diagnostics; Cost-effectiveness analysis; Costs; Cross-validation; Cutoff selection; Decision analytic modeling; Deep learning; Definitions; Denaturation; Diagnostics; Digital biomarker; Drug approval; Drug development; Drug-diagnostic codevelopment; Drug–diagnostic codevelopment; EGFR; Erbb2; Ethnic groups; European Medicines Agency; European regulation; FISH; Formalin-fixation; FoundationFocus CDxBRCA assay; FoundationOne CDx; Gene enumeration; Genomics; Genotyping; Health outcomes; Heart failure; Hyaluronic acid; Hybridization; IDE; IDE submission; IHC; IQFISH; IRB; IUO; IVD; Immuno-PET imaging; Immunohistochemistry; In vitro diagnostic; In vitro diagnostics; Innovative Device Pathway; Investigational device; Japan; Laboratory-developed test; Labour; Linked evidence approach; Liquid biopsies; Liquid biopsy; Lung; Lung cancer; MHLW; Machine learning; Markov; Mass spectrometry; Melanoma; Ministry of Health; Molecular diagnostic techniques; Multiscale modeling; NGS; NSCLC; Next-generation sequencing; Nonhealth outcomes