Lung Cancer Clinical Trials with a Seamless Phase II/III Design: Systematic Review

Dionysios Palermos1, Theodoros N Sergentanis1,2, Maria Gavriatopoulou1

  • 1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, 11528 Athens, Greece.

Insights

Seamless phase II/III designs offer a flexible and efficient approach for lung cancer clinical trials, reducing sample size and development time. This adaptive methodology is proving suitable for evaluating novel targeted therapies and immunotherapies in advanced lung cancer.

Area of Science:

  • Oncology
  • Clinical Trial Design
  • Translational Research

Background:

  • Lung cancer research prioritizes biomarkers and personalized medicine.
  • Adaptive clinical trial designs offer enhanced flexibility over traditional models.
  • Seamless phase II/III designs aim to optimize drug development by reducing sample size and time.

Purpose of the Study:

  • To systematically identify and characterize lung cancer clinical trials utilizing seamless phase II/III designs.
  • To analyze the methodologies and endpoints of these adaptive trials.

Main Methods:

  • Algorithmic systematic search of major biomedical databases (MEDLINE, SCOPUS, EMBASE, Cochrane) until June 2022.
  • Screening of 1420 records, with 28 eligible trials included in the systematic review.
  • Categorization of trials based on study endpoints, such as inefficacy/futility analyses and dose escalation.

Main Results:

  • The review identified 28 eligible lung cancer trials employing seamless phase II/III designs.
  • Most common subtypes included inefficacy/futility analyses (61%) and dose escalation (18%).
  • Eligible trials predominantly featured open-label, non-small cell lung cancer patients with advanced disease, evaluating targeted therapies and immunotherapies.

Conclusions:

  • Seamless phase II/III designs are a feasible and effective approach in lung cancer research.
  • This adaptive design methodology supports the evaluation of novel treatments, including targeted therapies and immunotherapies.
  • Distinct subcategories of seamless phase II/III designs exist, tailored to specific study endpoints.

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