Cancer Informatics: Essential Technologies for Clinical Trials by John S. SilvaCancer Informatics: Essential Technologies for Clinical Trials by John S. Silva

Cancer Informatics: Essential Technologies for Clinical Trials

byJohn S. SilvaEditorJohn S. Silva, Marion J. Ball

Paperback | September 12, 2012

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Cancer Informatics: Essential Technologies for Clinical Trials describes the National Cancer Institute-s vision of a Cancer Informatics Infrastructure (CII). By exploiting the best that the Internet and information technology have to offer, the CII will facilitate clinical trials, for all who are involved, including the patient along with the myriad of health professionals involved in cancer trials. To bridge the chasm between discoveries and best clinical practices, the editors describe the CII and how it can function to expedite the clinical trial life cycle, facilitate faster and safer drug development, and make more appropriate treatment choices available to cancer patients. Presented in four comprehensive sections edited by leading experts, the book highlights: - E-commerce - Digital libraries - Standards development - Public health informatics - Common data elements (CDEs) - Clinical trials information systems - Consumer education and support Cancer Informatics: Essential Technologies for Clinical Trials is an indispensable guide to clinical trials. Its contributors speak to oncologists and primary care physicians, as well as researchers, trial managers, administrators, informaticians, and consumers. Today, science is extending our knowledge of genes, proteins, and pathways, and pharmaceutical companies are developing more and more new therapies. In this rapidly changing world, the technologies that cancer informatics provides are essential to efforts to translate cancer research into cancer care, control, and, ultimately, prevention. John S. Silva, M.D., Center for Bioinformatics, National Cancer Institute Marion J. Ball, Ed.D., Vice President, Clinical Solutions, Healthlink, Inc.; Adjunct Professor, The Johns Hopkins University School of Nursing Christopher G. Chute, M.D., Dr.P.H., Professor of Medical Informatics, Head, Section of Medical Information Resources, Mayo Clinic Judith V. Douglas, M.A., M.H.S., formerly Associate, First Consulting Group Curtis P. Langlotz, M.D., Ph.D., Assistant Professor of Radiology, Epidemiology, and Computer and Information Science, University of Pennsylvannia Joyce. C. Niland, Ph.D., Chair, Division of Information Sciences, Director, Department of Biostatistics, City of Hope National Medical Center William L. Scherlis, Ph.D., Principal Research Scientist, School of Computer Science, Carnegie Mellon University
Title:Cancer Informatics: Essential Technologies for Clinical TrialsFormat:PaperbackDimensions:377 pagesPublished:September 12, 2012Publisher:Springer NatureLanguage:English

The following ISBNs are associated with this title:

ISBN - 10:1461265479

ISBN - 13:9781461265474

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Table of Contents

Foreword, Series Preface, Preface, Acknowlegements, Dedication, Section 1. The Vision, Section Introduction: Supporting Clinical Trials with a Cancer Informatics Infrastructure, Chapter 1. Translating Cancer Research into Cancer Care, Chapter 2. Visions of the Future, Chapter 3. Clinical Trials in Practice, Section 2. The Infrastructure, Section Introduction: Developing and Improving the Informatics Infrastructure to Support Clinical Research, Chapter 4. Cancer Informatics: Lessons from the World of E-Business, Chapter 5. Security and Privacy, Chapter 6. Digital Libraries and Scholarly Communication, Section 3. Standards and Vocabulary, Section Introduction: The Spectrum of Existing and Emerging Health Data Standards: Their Relevance and Application to Cancer Information, Chapter 7. Cancer Data, Information Standards, and Convergent Efforts, Chapter 8. Toward Terminology as Infrastructure, Chapter 9. Clinical Terminologies for Data Analysis and Structured Data Entry, Chapter 10. Information Standards Within NCI, Chapter 11. CDE Development Model for Chest CT Screening for Lung Cancer, Chapter 12. Pathology Standards in Cancer Informatics, Chapter 13. Clinical Information Interchange with Health Level Seven, Chapter 14. The Health Level Seven Reference Information Model, Chapter 15. HIPAA Administrative Simplification Standards: Provisions of the Final Privacy Rule Related to Clinical Trials, Chapter 16. Toward a Shared Representation of Clinical Trial Protocols: Application of the GLIF Guideline Modeling Framework, Chapter 17. Informatics for Cancer Prevention and Control, Section 4. The Vision, Section Introduction: Moving Toward the Vision: Putting Applications in Place, Chapter 18. Selection of Oncology Information Systems, Chapter 19. Clinical State Diagrams and Informatics Tools for Clinical Trial Protocols, Chapter 20. Support for the Cancer Patient: An Internet Model, Chapter 21. Increasing Clinical Trials Awareness and Accrual Via the Web, Chapter 22. ClinicalTrials.gov: Linking Patients to Medical Research, Chapter 23. The National Cancer Institute's net-Trials, Chapter 24. iN: A Community-Based Cancer Informatics and Clinical Trials Network, Chapter 25. Consumer Health Informatics, Chapter 26. An Internet-Based Data System for Outcomes Research

Editorial Reviews

From the reviews:"People running cancer trials should read this book. It is about the US National Cancer Institute's plans to 'liberate cancer trials from paper'. . The chapters were written by leading US experts. The content is detailed, technical, and surprisingly well-written. They give a clear vision of how cancer trials are likely to develop over the next 20 years. This book is informative, interesting, and . enjoyable." (M Stockler, Cancer Forum, Vol. 27 (3), 2003)