Phase I Oncology Drug Development / Timothy A. Yap, Jordi Rodon, David S. Hong, editors.

This book provides a detailed review of how oncology drug development has changed over the past decade, and serves as a comprehensive guide for the practicalities in setting up phase I trials. The book covers strategies to accelerate the development of novel antitumor compounds from the laboratory t...

Full description

Saved in:
Bibliographic Details
Other Authors: Yap, Timothy A. (Editor), Rodon, Jordi (Editor), Hong, David S. (Editor)
Format: eBook
Language:English
Published: Cham : Springer, 2020.
Subjects:
Online Access:Click for online access

MARC

LEADER 00000cam a2200000 i 4500
001 on1203802613
003 OCoLC
005 20240808213014.0
006 m o d
007 cr |||||||||||
008 200918s2020 sz o 001 0 eng d
040 |a NLW  |b eng  |e pn  |c NLW  |d EBLCP  |d OCLCO  |d YDX  |d LQU  |d UPM  |d OCLCF  |d GW5XE  |d GZM  |d N$T  |d OCLCO  |d UKAHL  |d OCL  |d OCLCQ  |d OCLCO  |d COM  |d OCLCQ  |d UKMGB  |d OCLCQ  |d OCLCO  |d OCLCQ 
015 |a GBC338044  |2 bnb 
016 7 |a 019944381  |2 Uk 
019 |a 1196837368  |a 1197838513  |a 1202456427 
020 |a 9783030476823  |q (electronic bk.) 
020 |a 3030476820  |q (electronic bk.) 
020 |z 9783030476816  |q (print) 
020 |z 3030476812 
024 7 |a 10.1007/978-3-030-47682-3  |2 doi 
024 8 |a 10.1007/978-3-030-47 
035 |a (OCoLC)1203802613  |z (OCoLC)1196837368  |z (OCoLC)1197838513  |z (OCoLC)1202456427 
037 |a com.springer.onix.9783030476823  |b Springer Nature 
050 4 |a RC271.C5 
049 |a HCDD 
245 0 0 |a Phase I Oncology Drug Development /  |c Timothy A. Yap, Jordi Rodon, David S. Hong, editors. 
264 1 |a Cham :  |b Springer,  |c 2020. 
264 4 |c ©2020 
300 |a 1 online resource (352 pages) 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
500 |a Paradigm shift in oncology drug development.- Practicalities in setting up phase I trials.- Optimizing the preclinical development of antitumor agents for entry into phase I trials.- Considerations for the development of novel chemotherapies in phase I trials.- Considerations for the development of novel targeted agents in phase I trials.- Development of immunotherapeutic strategies in early phase clinical trials.- Assessment of radiotherapeutic strategies in phase I trials.- Development of combinatorial strategies in phase I trials.- Novel trial designs for early phase clinical trials.- Incorporating pharmacokinetic strategies for phase I trials.- Development of pharmacodynamic biomarkers for phase I trials.- Efficacy considerations for Phase I trials.- Incorporating precision medicine into Phase I clinical trials.- Molecular profiling of patients for clinical trials.- Incorporating circulating biomarkers into clinical trials.- Statistical considerations for early phase clinical trials.- Lessons from hematology for solid tumor drug development. 
506 1 |a Legal Deposit;  |c Only available on premises controlled by the deposit library and to one user at any one time;  |e The Legal Deposit Libraries (Non-Print Works) Regulations (UK).  |5 WlAbNL 
505 0 |a Paradigm shift in oncology drug development -- Practicalities in setting up phase I trials -- Optimizing the preclinical development of antitumor agents for entry into phase I trials -- Considerations for the development of novel chemotherapies in phase I trials -- Considerations for the development of novel targeted agents in phase I trials -- Development of immunotherapeutic strategies in early phase clinical trials -- Assessment of radiotherapeutic strategies in phase I trials -- Development of combinatorial strategies in phase I trials -- Novel trial designs for early phase clinical trials -- Incorporating pharmacokinetic strategies for phase I trials -- Development of pharmacodynamic biomarkers for phase I trials -- Efficacy considerations for Phase I trials -- Incorporating precision medicine into Phase I clinical trials -- Molecular profiling of patients for clinical trials -- Incorporating circulating biomarkers into clinical trials -- Statistical considerations for early phase clinical trials -- Lessons from hematology for solid tumor drug development. 
500 |a Includes index. 
520 |a This book provides a detailed review of how oncology drug development has changed over the past decade, and serves as a comprehensive guide for the practicalities in setting up phase I trials. The book covers strategies to accelerate the development of novel antitumor compounds from the laboratory to clinical trials and beyond through the use of innovative mechanism-of-action pharmacodynamic biomarkers and pharmacokinetic studies. The reader will learn about all aspects of modern phase I trial designs, including the incorporation of precision medicine strategies, and approaches for rational patient allocation to novel anticancer therapies. Circulating biomarkers to assess mechanisms of response and resistance are changing the way we are assessing patient selection and are also covered in this book. The development of the different classes of antitumor agents are discussed, including chemotherapy, molecularly targeted agents, immunotherapies and also radiotherapy. The authors also discuss the lessons that the oncology field has learnt from the development of hematology-oncology drugs and how such strategies can be carried over into therapies for solid tumors. There is a dedicated chapter that covers the specialized statistical approaches necessary for phase I trial designs, including novel Bayesian strategies for dose escalation. This volume is designed to help clinicians better understand phase I clinical trials, but would also be of use to translational researchers (MDs and PhDs), and drug developers from academia and industry interested in cancer drug development. It could also be of use to phase I trial study coordinators, oncology nurses and advanced practice providers. Other health professionals interested in the treatment of cancer will also find this book of great value. 
650 0 |a Antineoplastic agents  |x Design. 
650 0 |a Cancer  |x Chemotherapy. 
650 0 |a Drug development. 
650 0 |a Medicine. 
650 0 |a Oncology. 
650 0 |a Radiotherapy. 
650 7 |a medicines (material)  |2 aat 
650 7 |a medicine (discipline)  |2 aat 
650 7 |a Radiotherapy.  |2 bicssc 
650 7 |a Oncology.  |2 bicssc 
650 7 |a Medical  |x Radiology & Nuclear Medicine.  |2 bisacsh 
650 7 |a Medical  |x Oncology.  |2 bisacsh 
650 7 |a Medicine  |2 fast 
650 7 |a Drug development  |2 fast 
650 7 |a Cancer  |x Chemotherapy  |2 fast 
650 7 |a Antineoplastic agents  |x Design  |2 fast 
650 7 |a Oncology  |2 fast 
650 7 |a Radiotherapy  |2 fast 
655 0 |a Electronic books. 
700 1 |a Yap, Timothy A.,  |e editor. 
700 1 |a Rodon, Jordi,  |e editor. 
700 1 |a Hong, David S.,  |e editor. 
776 0 8 |i Print version:  |z 3030476812  |z 9783030476816  |w (OCoLC)1150925723 
856 4 0 |u https://holycross.idm.oclc.org/login?auth=cas&url=https://link.springer.com/10.1007/978-3-030-47682-3  |y Click for online access 
903 |a SPRING-MED2020 
994 |a 92  |b HCD