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El. knyga: Phase I Cancer Clinical Trials: A Practical Guide

Edited by (Head, Department of Oncology; Medical Director, Oncology Program, Queen's University, Kingston General Hospital, Cancer Centre of Southeastern Ontario, Kingston, Ontario, Canada), Edited by , Edited by (Professor of Clinical Pharmacology and Oncology; Head, )
  • Formatas: 352 pages
  • Išleidimo metai: 20-Mar-2015
  • Leidėjas: Oxford University Press Inc
  • Kalba: eng
  • ISBN-13: 9780199359028
Kitos knygos pagal šią temą:
  • Formatas: 352 pages
  • Išleidimo metai: 20-Mar-2015
  • Leidėjas: Oxford University Press Inc
  • Kalba: eng
  • ISBN-13: 9780199359028
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Phase I trials are a critical first step in the study of novel cancer therapeutic approaches. Their primary goals are to identify the recommended dose, schedule and pharmacologic behavior of new agents or new combinations of agents and to describe the adverse effects of treatment. In cancer therapeutics, such studies have particular challenges. Due to the nature of the effects of treatment, most such studies are conducted in patients with advanced malignancy, rather than in healthy volunteers. Further, the endpoints of these trials are usually measures adverse effects rather than molecular target or anti-tumor effects. These factors render the design, conduct, analysis and ethical aspects of phase I cancer trials unique. As the only comprehensive book on this topic, Phase I Cancer Clinical Trials is a useful resource for oncology trainees or specialists interested in understanding cancer drug development. New to this edition are chapters on Phase 0 Trials and Immunotherapeutics, and updated information on the process, pitfalls, and logistics of Phase I Trials

Recenzijos

This is a well-written, well-structured book that comprehensively covers the unique aspects of phase I clinical trials in cancer patients. This may be the only book of its kind and will be appropriate for a wide audience. * Karen L. Reckamp, MD, MS; Doodys Reviews *

Preface vii
Contributors ix
1 Introduction
1(8)
Elizabeth A. Eisenhauer
2 Preclinical Data and Requirements
9(35)
Sophie Postel-Vinay
Jean-Charles Soria
Elizabeth A. Eisenhauer
3 Phase 0 Clinical Trials
44(13)
Shivaani Kummar
James H. Doroshow
4 Basics of Phase I Design: First-in-Human Studies
57(34)
Donna M. Graham
Aaron R. Hansen
Elizabeth A. Eisenhauer
Lillian L. Siu
5 Ethical Issues in First-in-Human Phase I Cancer Trials
91(13)
Elizabeth A. Eisenhauer
6 Phase I Trials in Special Populations and Circumstances
104(45)
Rajiv Kumar
Chris Twelves
Udai Banerji
7 Phase I Trials of Immunotherapeutics
149(21)
Christy Ralph
Emma King
Chris Twelves
Christian Ottensmeier
8 Statistical Designs for First-in-Man Phase I Cancer Trials
170(30)
Xavier Paoletti
Marc Buyse
9 Writing the Protocol
200(27)
Penelope A. Bradbury
Elizabeth A. Eisenhauer
10 Practical Aspects of Pharmacokinetics and Pharmacodynamics
227(46)
Chris Twelves
Maria Jove
Paul Loadman
11 Process, Pitfalls, and Logistics of Phase I Trials
273(35)
Elizabeth A. Eisenhauer
Chris Twelves
Hayley Farmer
Philip Ross
12 Reporting and Interpreting Results
308(31)
Lesleigh S. Abbott
Elizabeth A. Eisenhauer
Lesley K. Seymour
Appendix: Useful Web Resources 339(4)
Index 343
EAE: Head, Department of Oncology, Queen's University, Medical Director, Oncology Program, Kingston General Hospital, Cancer Centre of Southeastern Ontario, Kingston, Canada; CT: Professor of Clinical Pharmacology and Oncology, Head, Section of Clinical Cancer Research Groups, Leeds Institute of Cancer Studies and Pathology, St. James's Institute of Oncology Leeds, UK; MB: Founder and Chairman, International Drug Development Institute, Louvain-la-Neuve, Belgium, Associate Professor of Biostatistics, Universiteit Hasselt Diepenbeek, Belgium