Difference between revisions of "Resource:4be659bc-2261-4e62-b4ed-d746e9f2c5be"

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|Resource Type=Cases
 
|Resource Type=Cases
 
|Title=Scientist Ousted From Cancer Study Declines to Testify to House Panel
 
|Title=Scientist Ousted From Cancer Study Declines to Testify to House Panel
|Is About=Data falsification in a series of studies which showed that lumpectomy was as effective as removing the entire breast for preventing recurrence in many women with early cancer. This is a factual case.
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|Is About=This is a factual case. This newspaper article describes a case of scientific misconduct in a series of studiesheaded by Bernard Fisher, that aimed to determine the best treatment for breast cancer. It was shown that one of the doctors responsible for admittance of patients to the trail committed fraud. The fraud included changing data to make patients eligible for inclusion in the study, even when they had explicitly stated that they did not want to participate.
|Important Because=To give insight in different ways of cheating in clinical trials.
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|Important Because=The article shows that fraud in clinical trials can happen in many forms and at various levels. Although the fraudulent actions sometimes may seem trivial, they can have a large impact. Cheating in a clinical trial may not only endanger the health of the patients participating in the study but also that of future patients.<ref name=":0">Baigent C, Harrell FE, Buyse M, Emberson JR, Altman DG. Ensuring trial validity by data quality assurance and diversification of monitoring methods. Clinical Trials. 2008;5(1):49-55. doi:10.1177/1740774507087554
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<br /></ref> As pointed out by the article, these malpractices in clinical trails may be more frequent than some scientific leaders are willing to publicly admit. Therefore, clinical trail data should be reviewed via a central statistical review by independent committees or algorithms designed for this purpose.<ref name=":0" />
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<references />
 
|Important For=researchers; research leaders; All stakeholders in research; phd students
 
|Important For=researchers; research leaders; All stakeholders in research; phd students
 
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{{Tags
 
{{Tags
|Involves=Roger Poisson; Bernard Fisher
 
 
|Has Timepoint=1985-1990
 
|Has Timepoint=1985-1990
 
|Has Location=Canada
 
|Has Location=Canada

Latest revision as of 08:46, 30 April 2021

Cases

Scientist Ousted From Cancer Study Declines to Testify to House Panel

What is this about?

This is a factual case. This newspaper article describes a case of scientific misconduct in a series of studiesheaded by Bernard Fisher, that aimed to determine the best treatment for breast cancer. It was shown that one of the doctors responsible for admittance of patients to the trail committed fraud. The fraud included changing data to make patients eligible for inclusion in the study, even when they had explicitly stated that they did not want to participate.

Why is this important?

The article shows that fraud in clinical trials can happen in many forms and at various levels. Although the fraudulent actions sometimes may seem trivial, they can have a large impact. Cheating in a clinical trial may not only endanger the health of the patients participating in the study but also that of future patients.[1] As pointed out by the article, these malpractices in clinical trails may be more frequent than some scientific leaders are willing to publicly admit. Therefore, clinical trail data should be reviewed via a central statistical review by independent committees or algorithms designed for this purpose.[1]

  1. 1.0 1.1 Baigent C, Harrell FE, Buyse M, Emberson JR, Altman DG. Ensuring trial validity by data quality assurance and diversification of monitoring methods. Clinical Trials. 2008;5(1):49-55. doi:10.1177/1740774507087554

For whom is this important?

Other information

When
Where
Virtues & Values
Good Practices & Misconduct
Research Area
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