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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.
Abstract:
Current lung cancer clinical research focuses on biomarkers and personalized treatment strategies. Adaptive clinical trial designs have gained significant ground due to their increased flexibility, compared to the conventional model of drug development from phase I to phase IV trials. One such adaptive approach is the seamless phase II/III design, which has been used to reduce the total sample size and drug development time. In this context, an algorithmic systematic search was conducted in MEDLINE (PUBMED), SCOPUS, EMBASE and Cochrane Central Register of Controlled Trials until 31 June 2022 in order to identify lung cancer trials of systematic treatments that have employed the seamless phase II/III methodology and to describe their characteristics. The search strategy yielded a total of 1420 records that were screened through their title and abstract; 28 eligible trials were included in the systematic review. Based on the study endpoints, the most common subtype included phase II/III trials with inefficacy/futility analyses (61%; 17/28), followed by dose escalation phase II/III trials (18%; 5/28), one multi-arm multi stage trial and 5 trials with other design (18%). Most eligible trials were open-label (71%; 20/27), included patients with non-small cell lung cancer (82%; 23/28), evaluated targeted therapies and/or immunotherapies (82%; 23/28) and recruited patients with advanced disease (89.3%; 25/28). In conclusion, the seamless phase II/III design is a feasible and suitable approach in lung cancer research, with distinct design subcategories according to study endpoints.
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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