Factors influencing inclusion of patients with malignancies in clinical trials

Caroline Tournoux1, Sandrine Katsahian, Sylvie Chevret

  • 1Department of Biostatistics, Hospital Saint Louis, APHP, Paris, France.

Cancer
|January 7, 2006
PubMed

Insights

Low patient participation in oncology clinical trials stems from patient preferences, consent concerns, and protocol issues. Addressing these barriers requires targeted strategies for both patients and clinicians to improve trial recruitment.

Area of Science:

  • Oncology
  • Clinical Trials
  • Health Services Research

Background:

  • Patient participation in clinical trials is a significant challenge in oncology.
  • Low recruitment rates hinder the advancement of cancer treatments and research.

Purpose of the Study:

  • To systematically review and identify barriers to patient recruitment in oncology clinical trials.
  • To categorize these barriers based on patient-related, clinician-related, and other factors.

Main Methods:

  • A systematic review of 75 papers published up to August 2004 was conducted.
  • Barriers were analyzed and categorized based on their source (patient, clinician, other) and specific nature.

Main Results:

  • Patient-related factors (44%) included preference, information/consent concerns, and uncertainty. Clinician-related factors (37%) involved protocol incompatibility and consent procedures.
  • Other factors (49%) frequently cited specific patient groups, such as age and minority populations, particularly in North American studies.
  • Clinician-related factors were reported more frequently in papers published before 1995.

Conclusions:

  • Patient and clinician-related factors significantly impede oncology clinical trial recruitment.
  • Addressing barriers like patient preferences, consent issues, and protocol complexities is crucial.
  • Developing and evaluating targeted strategies is essential to enhance patient enrollment in clinical trials.

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