Evaluation of Oncology Trial Results Reporting Over a 10-Year Period

Xu Liu1,2, Yuan Zhang1,2, Wen-Fei Li1

  • 1Department of Radiation Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center of Cancer Medicine, Guangzhou, Guangdong, China.

JAMA Network Open
|May 24, 2021
PubMed
Abstract

Insights

Reporting of clinical trial results for oncology studies improved over a decade, with registries offering a platform for unpublished data. This enhances transparency and patient rights in cancer research.

Area of Science:

  • Oncology
  • Clinical Trials
  • Biostatistics

Background:

  • Unreported clinical trial results violate human rights.
  • Oncology trials constitute a significant portion of biopharmaceutical studies.

Purpose of the Study:

  • To analyze the reporting rates of interventional oncology trials registered on ClinicalTrials.gov between 2007 and 2017.

Main Methods:

  • A cohort study analyzed 12,240 oncology trials registered on ClinicalTrials.gov.
  • Results reporting was assessed within 24 months of trial completion.
  • Publication data was verified through ClinicalTrials.gov, PubMed, and Embase.

Main Results:

  • 60.7% of trials reported results, with a 34% increase in reporting rates from 2007-2017.
  • Factors influencing reporting included trial recency, sample size, funding source, and completion status.
  • 37.8% of reported results were posted only on ClinicalTrials.gov, often for terminated or small trials.

Conclusions:

  • Oncology trial results reporting has gradually improved over ten years.
  • Clinical trial registries can serve as platforms for reporting unpublished results.
  • Registries can also function as valuable data sources for future research.

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