Landscape survey of non-small-cell lung carcinoma (NSCLC) for immuno-oncology (IO)
Overview
Immuno-oncology (IO) has significantly transformed the treatment landscape for non-small-cell lung carcinoma (NSCLC), with therapies targeting immune checkpoints such as PD-1 and PD-L1 demonstrating promising clinical outcomes. However, identifying reliable biomarkers and understanding treatment efficacy across different therapy lines requires extensive analysis of clinical trial data and scientific literature.
Excelra partnered with a large pharmaceutical company to perform a comprehensive NSCLC immuno-oncology landscape survey, analyzing clinical studies and biomarker data to support clinical trial strategy. Leveraging advanced data curation services, bioinformatics solutions, and scientific informatics, Excelra developed a structured dataset from a wide range of clinical studies to uncover biomarker insights and treatment trends.
Our client
The client is a large pharmaceutical company based in the United States focused on developing new therapeutic strategies for non-small-cell lung cancer (NSCLC). Their research team aimed to identify biomarkers that could support the design of effective immuno-oncology clinical trials and improve patient outcomes.
Client’s challenge
Identifying suitable biomarkers for NSCLC immunotherapy requires extensive analysis of existing clinical trial data and scientific literature.
The client faced several challenges:
- Extracting NSCLC clinical trial data from large volumes of published literature
- Structuring heterogeneous datasets for meaningful analysis
- Identifying correlations between immune response biomarkers and clinical outcomes
- Evaluating checkpoint inhibitors targeting PD-1 and PD-L1 pathways
- Understanding treatment efficacy across multiple lines of therapy
Conducting this analysis manually would require significant time and resources, prompting the client to collaborate with Excelra for a comprehensive data analysis solution.
Client’s goals
The client sought to achieve the following objectives:
- Conduct a comprehensive landscape survey of NSCLC clinical trials
- Identify biomarkers that could guide immuno-oncology clinical trial design
- Evaluate checkpoint inhibitors targeting PD-1 and PD-L1
- Assess treatment outcomes across multiple therapy lines
- Gain insights into immune response mechanisms and tumor-infiltrating lymphocytes (TILs)
Our approach
Literature identification using text mining
Excelra developed a text-mining algorithm to identify relevant literature and clinical studies related to NSCLC immunotherapies. This automated approach enabled rapid extraction of relevant publications from large scientific databases.
Data curation and annotation
Once relevant studies were identified, Excelra’s scientific experts manually curated and annotated the data. According to the curated dataset, 82 relevant clinical studies were analyzed across multiple parameters including therapy lines, immune profiles, and biomarker correlations.
Key curated data points included:
- Line of therapy
- Circulating immune cell profile
- Tumor-infiltrating lymphocytes (TILs)
- PD-L1 expression assays
- Baseline mutation status
- Correlation between clinical response and immune markers
Clinical trial landscape analysis
Excelra’s analysis focused on checkpoint inhibitors targeting PD-1 and PD-L1, evaluating their efficacy across four lines of therapy:
- Naïve patients
- First-line therapy
- Second-line therapy
- Third-line therapy
The compiled landscape dataset included detailed information about drugs, treatment regimens, and efficacy-related endpoints.
Comparative immunotherapy analysis
Excelra conducted comparative analyses between anti-PD-1 and anti-PD-L1 therapies, identifying similarities and unique efficacy endpoints across treatments. The analysis revealed several correlations between PD-L1 expression levels, immune cell profiles, and clinical response rates.
Figure 1: Summary of the compiled NSCLC landscape for pembrolizumab
Table: Treatment regimen for NSCLC and the measured clinical response
Our solution
Excelra delivered a comprehensive NSCLC immuno-oncology landscape dataset that enabled the client to make informed decisions regarding biomarker selection and clinical trial design.
Key outcomes
- Curated dataset of 82 NSCLC clinical studies
- Identification of biomarkers associated with immune response and treatment outcomes
- Comparative analysis of anti-PD-1 and anti-PD-L1 therapies
- Insights into tumor-infiltrating lymphocyte (TIL) profiles and immune cell dynamics
- Structured analysis of treatment regimens across therapy lines
The analysis also highlighted trends in PD-L1 assays and tumor proportion score (TPS) correlations with clinical response across multiple therapy stages.
Key benefits
- Accelerated biomarker discovery
The curated NSCLC dataset enabled faster identification of biomarkers relevant to immunotherapy clinical trials. - Improved clinical trial strategy
Comprehensive analysis of therapy lines and treatment regimens supported optimized trial design. - High-Quality Analysis-Ready data
Excelra delivered structured datasets ready for downstream analysis and research applications.
Figure 3: Anti-PD-1 and anti-PD-L1 treatment and efficacy data points. Blue data points are common
for both anti-PD-1 and anti-PD-L1. Orange data points are unique to anti-PD-1
Figure 4: Comparative analysis of efficacy endpoints between different lines of therapy
Figure 5: PD-L1 assays and association with the clinical response across different lines of therapy
Conclusion
Excelra’s comprehensive NSCLC immuno-oncology landscape survey provided the client with valuable insights into biomarker correlations, immune response mechanisms, and treatment efficacy across therapy lines. By integrating text mining, data curation, and clinical trial analysis, Excelra delivered analysis-ready data that supports clinical decision-making and accelerates oncology research.
For additional insights into Excelra’s expertise in biomedical data analysis, explore resources such as big data in drug discovery or related case studies.
