Data-Based Radiation Oncology - Design of Clinical Trials (Record no. 3018963)

MARC details
000 -LEADER
fixed length control field 03246naaaa2200361uu 4500
001 - CONTROL NUMBER
control field https://directory.doabooks.org/handle/20.500.12854/44556
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220714193839.0
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 978-2-88945-438-9
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9782889454389
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.3389/978-2-88945-438-9
Terms of availability doi
041 0# - LANGUAGE CODE
Language code of text/sound track or separate title English
042 ## - AUTHENTICATION CODE
Authentication code dc
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name S
Relator code auth
245 10 - TITLE STATEMENT
Title Data-Based Radiation Oncology - Design of Clinical Trials
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Name of publisher, distributor, etc Frontiers Media SA
Date of publication, distribution, etc 2018
300 ## - PHYSICAL DESCRIPTION
Extent 1 electronic resource (109 p.)
506 0# - RESTRICTIONS ON ACCESS NOTE
Terms governing access Open Access
Source of term star
Standardized terminology for access restriction Unrestricted online access
520 ## - SUMMARY, ETC.
Summary, etc In radiation oncology as in many other specialties clinical trials are essential to investigate new therapy approaches. Usually, preparation for a prospective clinical trial is extremely time consuming until ethics approval is obtained. To test a new treatment usually many years pass before it can be implemented in the routine care. During that time, already new interventions emerge, new drugs appear on the market, technical & physical innovations are being implemented, novel biology driven concepts are translated into clinical approaches while we are still investigating the ones from years ago. Another problem is associated with molecular diagnostics and the growing amount of tumor specific biomarkers which allows for a better stratification of patient subgroups. On the other side, this may result in a much longer time for patient recruiting and consequently in larger multicenter trials. Moreover, all of the relevant data must be readily available for treatment decision making, treatment as well as follow-up, and ultimately for trial evaluation. This challenges even more for agreed standards in data acquisition, quality and management. How could we change the way currently clinical trials are performed in a way they are safe and ethically justifiable and speed up the initiation process, so we can provide new and better treatments faster for our patients? Further, while we rely on various quantitative information handling distributed, large heterogeneous amounts of data efficiently is very important. Thus data management becomes a strong focus. A good infrastructure helps to plan, tailor and conduct clinical trials in a way they are easy and quickly analyzable. In this research topic we want to discuss new ideas for intelligent trial designs and concepts for data management.
540 ## - TERMS GOVERNING USE AND REPRODUCTION NOTE
Terms governing use and reproduction Creative Commons
-- https://creativecommons.org/licenses/by/4.0/
-- cc
-- https://creativecommons.org/licenses/by/4.0/
546 ## - LANGUAGE NOTE
Language note English
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term Study Management
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term Clinical trials
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term Data Collection
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term Radiation Oncology
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term Clinical Study design
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kerstin A. Kessel
Relator code auth
9 (RLIN) 1620219
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Fridtjof Nuesslin
Relator code auth
9 (RLIN) 1620220
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Bhadrasain Vikram
Relator code auth
9 (RLIN) 1620221
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Anne W. Lee
Relator code auth
9 (RLIN) 1620222
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Stephanie E. Combs
Relator code auth
9 (RLIN) 1620223
856 40 - ELECTRONIC LOCATION AND ACCESS
Host name www.oapen.org
Uniform Resource Identifier <a href="https://www.frontiersin.org/research-topics/4727/data-based-radiation-oncology---design-of-clinical-trials">https://www.frontiersin.org/research-topics/4727/data-based-radiation-oncology---design-of-clinical-trials</a>
-- 0
Public note DOAB: download the publication
856 40 - ELECTRONIC LOCATION AND ACCESS
Host name www.oapen.org
Uniform Resource Identifier <a href="https://directory.doabooks.org/handle/20.500.12854/44556">https://directory.doabooks.org/handle/20.500.12854/44556</a>
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Public note DOAB: description of the publication
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