Abstract

In planning a clinical trial for demonstrating the efficacy of pioglitazone to resolve leukoplakia and erythroplakia in Fanconi anemia patients we had to discuss the need for a randomized controlled trial particularly under sample-size restrictions as very promising results were available from a single-arm clinical trial. Unfortunately, at a later stage, we had to suffer from the fact that single-arm clinical trials may sometimes mislead. When revisiting our planning at a later stage of a grant application, results of a randomized controlled trial had become available which were less impressive, but may still be of clinical interest. However, these results were perceived as disappointing in the light of previously raised hopes based on the results of the single-arm trial. We highlight some major problems when research is based on single-arm trials compared to randomized controlled trials. After debunking common arguments for the conduct of single-arm trials in rare disease we conclude that particularly in rare disease research should be based on randomized building blocks simply because more robust evidence is generated. The plea for single-arm trials should be substituted by a plea for cooperation of all stakeholders to provide best evidence for decision making under sample-size restrictions.

Highlights

  • Randomized controlled trials (RCTs) with one control arm and at least one new treatment arm are the gold standard to inform about treatment efficacy, safety, and benefit-/risk-ratio

  • Lasch et al Orphanet Journal of Rare Diseases (2017) 12:102 response in a control group) derived from registries or historical controls raises two issues: 1. The estimated difference between treatment and counterfactual might be biased and the potential drawbacks of using historical controls or registries have been discussed in many places [5, 6] and apply here

  • When illustrating the global view of study planning, we focus on single-arm trials as antagonists of RCTs

Read more

Summary

Introduction

Randomized controlled trials (RCTs) with one control arm and at least one new treatment arm are the gold standard to inform about treatment efficacy, safety, and benefit-/risk-ratio. Every time a single-arm trial is conducted, the researchers assume that the outcome in the control group (placebo or standard of care) is entirely known and not subjected to patient selection, or temporal effects.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call