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New research in the December 2021 issue of JNCCN—Journal of the National Comprehensive Cancer Network found that only 59% of oncology clinical trials studied provided adequately-defined rules for censoring. The researchers examined published randomized control trials supporting FDA approval for treatments for solid tumors from January 2015 through December 2019—and found that for 33 out of 81 studies, it was not clear in the publication why or how patients were being censored.

Censoring is defined in this context as the practice of removing patients from follow-up before experiencing the outcome of interest; for instance, if the main outcome of a cancer treatment trial is survival and the patient experiences a heart attack and withdraws from the trial, they may no longer be followed-up. If the proportion of patients who are censored is not evenly balanced between comparison groups, indocin for arthritis pain this can introduce bias and makes it difficult to interpret the results of trials.

“We hope that our findings will prompt investigators and journals to report early drug discontinuation, withdrawal of consent, loss to follow-up, and censoring more transparently in trial publications. This would allow patients and clinicians to make more informed decisions regarding the potential benefits of a treatment,” said lead researcher Brooke E. Wilson, MBBS, MSc, University of Toronto. “Regulatory authorities and journals can play a leadership role in mandating improved transparency and ensuring that censoring data be made publicly available.”

The authors compiled a list of goals and recommendations to improve transparency and reporting in clinical trials. Those goals include:

  • Minimize the chance of post-randomization bias
  • Improve transparency regarding censoring methods in oncology trials
  • Explore the impact of censoring on trial results
  • Improve the handling of transparency of missing outcome data in trial results
  • Acknowledge the potential impact of censoring on the interpretation of results
  • Provide transparent information regarding early drug discontinuation and withdrawal of consent or loss to follow-up

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