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Neoantigens in Cancer Immunotherapy: An Overview with a Focus on Non-small Cell Lung Cancer and Pancreatic Ductal
Fatemeh Eskandari-Malayeri1, Sajjad Shekarchian1, Esmaeil Mortaz2
1Department of Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. emortaz@gmail.com.
Abstract:
Non-small cell lung cancer (NSCLC) and pancreatic ductal adenocarcinoma (PDAC) figure prominently in the list of prevalent and resistant cancers that reveal significant differences in response to immunotherapy. Neoantigens, specific antigens resulting from tumor mutations, play an important role in provoking immune responses and the success of immunotherapy. This review scrutinizes the quantitative and qualitative differences in neoantigens in NSCLC and PDAC and their impact on the efficacy of immunotherapy. The evidence suggests that the higher mutational burden, greater diversity, and different quality of neoantigens in NSCLC compared with PDAC are among the key drivers contributing to the enhanced susceptibility to immunotherapy in this cancer. These differences could pave the way for the development of personalized therapies and novel strategies to improve treatment outcomes in resistant cancers.
Insights
Non-small cell lung cancer (NSCLC) shows better immunotherapy response than pancreatic ductal adenocarcinoma (PDAC) due to higher quality and quantity of neoantigens. These findings may guide personalized cancer treatments.
Area of Science:
- Oncology
- Immunology
- Cancer Genomics
Background:
- Non-small cell lung cancer (NSCLC) and pancreatic ductal adenocarcinoma (PDAC) are prevalent cancers with differing responses to immunotherapy.
- Neoantigens, arising from tumor mutations, are crucial for effective anti-tumor immune responses and immunotherapy success.
Purpose of the Study:
- To compare quantitative and qualitative differences in neoantigens between NSCLC and PDAC.
- To investigate the impact of these neoantigen differences on immunotherapy efficacy.
Main Methods:
- Review of existing literature and data comparing neoantigen profiles in NSCLC and PDAC.
- Analysis of factors contributing to immunotherapy response variations between these cancer types.
Main Results:
- NSCLC exhibits a higher mutational burden, greater neoantigen diversity, and distinct neoantigen quality compared to PDAC.
- These neoantigen characteristics in NSCLC are associated with enhanced susceptibility to immunotherapy.
Conclusions:
- Differences in neoantigen landscape significantly influence immunotherapy outcomes in NSCLC versus PDAC.
- Understanding these disparities can inform the development of personalized therapies for resistant cancers like PDAC.
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