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Checkpoint Blockade in Lung Cancer and Mesothelioma
Lysanne A Lievense1,2, Daniel H Sterman3, Robin Cornelissen1
11 Department of Pulmonary Medicine, Erasmus Medical Center Cancer Institute, Rotterdam, the Netherlands.
Abstract:
In the last decade, immunotherapy has emerged as a new treatment modality in cancer. The most success has been achieved with the class of checkpoint inhibitors (CPIs), antibodies that unleash the antitumor immune response. After the success in melanoma, numerous clinical trials are being conducted investigating CPIs in lung cancer and mesothelioma. The programmed death protein (PD) 1-PD ligand 1/2 pathway and cytotoxic T lymphocyte-associated protein 4 are currently the most studied immunotherapeutic targets in these malignancies. In non-small cell lung cancer, anti-PD-1 antibodies have become part of the approved treatment arsenal. In small cell lung cancer and mesothelioma, the efficacy of checkpoint inhibition has not yet been proven. In this Concise Clinical Review, an overview of the landmark clinical trials investigating checkpoint blockade in lung cancer and mesothelioma is provided. Because response rates are around 20% in the majority of clinical trials, there is much room for improvement. Predictive biomarkers are therefore essential to fully develop the potential of CPIs. To increase efficacy, multiple clinical trials investigating the combination of cytotoxic T lymphocyte-associated protein 4 inhibitors and PD-1/PD ligand 1 blockade in lung cancer and mesothelioma are being conducted. Given the potential benefit of immunotherapy, implementation of current and new knowledge in trial designs and interpretation of results is essential for moving forward.
Insights
Immunotherapy, including checkpoint inhibitors (CPIs), shows promise in lung cancer and mesothelioma. Further research and biomarkers are crucial to improve the current 20% response rates for these cancers.
Area of Science:
- Oncology
- Immunology
- Clinical Trials
Background:
- Immunotherapy, particularly checkpoint inhibitors (CPIs), has revolutionized cancer treatment.
- CPIs unleash the body's immune response against tumors.
- CPIs are being investigated for lung cancer and mesothelioma, building on success in melanoma.
Purpose of the Study:
- To provide an overview of landmark clinical trials for CPIs in lung cancer and mesothelioma.
- To highlight the need for improved efficacy and predictive biomarkers for CPIs.
- To discuss combination therapies and future directions in immunotherapy for these cancers.
Main Methods:
- Review of landmark clinical trials investigating CPIs in lung cancer and mesothelioma.
- Analysis of response rates and efficacy of programmed death protein (PD)-1/PD-ligand 1 and cytotoxic T lymphocyte-associated protein 4 (CTLA-4) pathways.
- Exploration of ongoing trials combining different CPIs.
Main Results:
- Anti-PD-1 antibodies are approved for non-small cell lung cancer.
- Efficacy of checkpoint inhibition is not yet proven for small cell lung cancer and mesothelioma.
- Current clinical trials show response rates around 20%, indicating room for improvement.
Conclusions:
- Predictive biomarkers are essential to maximize the potential of CPIs.
- Combination therapies (e.g., CTLA-4 and PD-1/PD-L1 blockade) are under investigation to enhance efficacy.
- Integrating new knowledge into trial design and interpretation is vital for advancing immunotherapy in lung cancer and mesothelioma.
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