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Making progress in early breast cancer: Taking time or accepting risk?

Abstract:
Outcomes for patients diagnosed with early breast cancer in developed countries have improved substantially over recent decades. Adjuvant therapies have contributed to this improvement and their benefits have been confirmed in large randomised controlled trials (RCTs) and meta-analyses. Lower event rates, whilst welcome, have created problems for RCTs, that need to be larger and often take longer to provide a reliable result. In an effort to maintain the rate of progress and to obviate the complexity, cost and time required to conduct large RCTs, there has been an increased tendency to rely on observational data to determine a treatment effect and also to accelerate progress by the use of a surrogate marker (pathological complete remission after neoadjuvant chemotherapy). We highlight the pitfalls in these approaches and suggest some simplifications in the conduct of RCTs.
Publication status:
Published
Peer review status:
Peer reviewed

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Institution:
University of Oxford
Division:
MSD
Department:
Nuffield Department of Population Health
Sub department:
Clinical Trial Service Unit
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Nuffield Department of Population Health
Sub department:
Population Health
Role:
Author


Publisher:
Elsevier
Journal:
European Journal of Cancer More from this journal
Volume:
78
Pages:
24-27
Publication date:
2017-04-01
Acceptance date:
2017-03-06
DOI:
EISSN:
1879-0852
ISSN:
0959-8049


Keywords:
Pubs id:
pubs:689247
UUID:
uuid:374ab942-9529-48d9-96db-5e2369be39ad
Local pid:
pubs:689247
Deposit date:
2017-04-18

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