Literature DB >> 9564167

[Clinical studies in oncology. Relevance, design, ethical considerations].

B Wörmann1, G Wulf, W Hiddemann.   

Abstract

BACKGROUND: Clinical research in oncology includes the evaluation of diagnostic, prognostic and therapeutic parameters in order to establish standards for the different tumor entities. Prerequisite is the retrospective and prospective analysis of large patient groups with established statistical methods. New potentially better strategies have to be compared in randomised studies with the respective "gold standard". The central role of clinical studies for evaluation and optimisation of therapy can be considered as moral obligation to included the maximal possible number of patients in clinical studies. However, only a small number of tumor patients in Germany is treated in controlled clinical studies. Reasons are lack of organisational structures, but also ethical considerations. STUDY DESIGNS: In this article several models for clinical studies are discussed with respect to their statistical significance, indication, and potential ethical objections.
CONCLUSION: Aim of the discussion is to increase the acceptance of the necessity of clinical studies for evaluation and optimisation of therapeutic options in oncology.

Entities:  

Mesh:

Year:  1998        PMID: 9564167     DOI: 10.1007/BF03044837

Source DB:  PubMed          Journal:  Med Klin (Munich)        ISSN: 0723-5003


  14 in total

1.  Women resist trials to test marrow transplants.

Authors:  Gina Kolata
Journal:  N Y Times Web       Date:  1995-02-15

2.  The clinical trial.

Authors:  A B HILL
Journal:  Br Med Bull       Date:  1951       Impact factor: 4.291

3.  The Value of Mixed Vaccines in the Prevention of the Common Cold.

Authors:  F R Ferguson; A F Davey; W W Topley
Journal:  J Hyg (Lond)       Date:  1927-03

4.  Clinical and prophylactic trials with assured new treatment for those at greater risk: II. Examples.

Authors:  M O Finkelstein; B Levin; H Robbins
Journal:  Am J Public Health       Date:  1996-05       Impact factor: 9.308

5.  Ethical and scientific features of cutoff-based designs of clinical trials: a simulation study.

Authors:  J C Cappelleri; W M Trochim
Journal:  Med Decis Making       Date:  1995 Oct-Dec       Impact factor: 2.583

6.  Sensitivity and specificity of clinical trials. Randomized v historical controls.

Authors:  H S Sacks; T C Chalmers; H Smith
Journal:  Arch Intern Med       Date:  1983-04

7.  Controversies in the management of non-small cell lung cancer: the results of an expert surrogate study.

Authors:  M J Palmer; B O'Sullivan; R Steele; W J Mackillop
Journal:  Radiother Oncol       Date:  1990-09       Impact factor: 6.280

8.  Clinical and prophylactic trials with assured new treatment for those at greater risk: I. A design proposal.

Authors:  M O Finkelstein; B Levin; H Robbins
Journal:  Am J Public Health       Date:  1996-05       Impact factor: 9.308

9.  An argument that all prerandomized clinical trials are unethical.

Authors:  D Marquis
Journal:  J Med Philos       Date:  1986-11

10.  A new design for randomized clinical trials.

Authors:  M Zelen
Journal:  N Engl J Med       Date:  1979-05-31       Impact factor: 91.245

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.