Drug repurposing for cancer treatments: a well-intentioned, but misguided strategy
Potential selection bias was mitigated by the exclusion of prevalent statin users and estimation of inverse probability weights for outcome models, and immortal-time bias was addressed by defining statin therapy initiation among survivors. [...]compared with previous studies, the study by Emilsson a...
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Published in | The lancet oncology Vol. 21; no. 9; pp. 1134 - 1136 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Ltd
01.09.2020
Elsevier Limited |
Subjects | |
Online Access | Get full text |
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Summary: | Potential selection bias was mitigated by the exclusion of prevalent statin users and estimation of inverse probability weights for outcome models, and immortal-time bias was addressed by defining statin therapy initiation among survivors. [...]compared with previous studies, the study by Emilsson and colleagues had more rigorous methodology. Emilsson and colleagues also observed that, as investigators allowed more time to define a statin user (ie, anyone who takes statins in the first 6, 12, or 18 months after a cancer diagnosis), the magnitude of benefit became more favourable. [...]the longer and more permissive the definition of statin use became, the more effective statins seemed to be, indicating the presence of immortal-time bias. Because these drugs lack single-agent activity in cancer, they cannot be assessed in uncontrolled, phase 2 studies, which is common in oncological research. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1470-2045 1474-5488 |
DOI: | 10.1016/S1470-2045(20)30424-1 |