Immune checkpoint inhibitors in driver mutation-positive nonsmall cell lung cancer
Rudolf M Huber1, Diego Kauffmann-Guerrero
1Ludwig-Maximilians-Universität München (LMU), University hospitals, Department of Medicine V, Division of Respiratory Medicine and Thoracic Oncology, Thoracic Oncology Centre Munich, Member of the German Center for Lung Research (DZL), Munich, Germany.
Purpose Of Review:
Immune checkpoint inhibitors (ICIs) and targeted therapies have changed the landscape of management of nonsmall cell lung cancer (NSCLC) dramatically. Whereas ICIs in NSCLC without specific driver mutations are well established it is unclear what the place of ICIs in driver mutation-positive NSCLC is. This review summarizes the current view on the use of ICIs in driver mutation-positive NSCLC.
Recent Findings:
Immune checkpoint inhibition in combination with chemotherapy (and antiangiogenesis) in recurrent driver mutation-positive NSCLC after tyrosine kinase inhibitor therapy may be effective.
Summary:
Currently the role of immune checkpoint inhibitors in driver mutation-positive NSCLC is limited. They can in combination be applied in second and later line settings if no specific therapy is available.
Insights
Immune checkpoint inhibitors (ICIs) show limited use in driver mutation-positive non-small cell lung cancer (NSCLC). Combination therapy with ICIs may be effective in later treatment lines when other options are unavailable.
Area of Science:
- Oncology
- Immunotherapy
- Genetics
Background:
- Non-small cell lung cancer (NSCLC) management has been transformed by targeted therapies and immune checkpoint inhibitors (ICIs).
- The efficacy of ICIs is established in NSCLC lacking specific driver mutations.
- The role of ICIs in driver mutation-positive NSCLC remains less clear.
Purpose of the Study:
- To review the current understanding of immune checkpoint inhibitor (ICI) utilization in driver mutation-positive non-small cell lung cancer (NSCLC).
- To clarify the place of ICIs in the treatment landscape for NSCLC with specific driver mutations.
Main Methods:
- Literature review of current research on immune checkpoint inhibitors and targeted therapies in NSCLC.
- Synthesis of evidence regarding the efficacy and limitations of ICIs in driver mutation-positive NSCLC.
Main Results:
- Immune checkpoint inhibition, particularly in combination with chemotherapy and antiangiogenesis, may offer benefits in recurrent driver mutation-positive NSCLC post-tyrosine kinase inhibitor therapy.
- Current data suggests a limited role for ICIs as a primary treatment in this patient group.
Conclusions:
- The application of immune checkpoint inhibitors in driver mutation-positive NSCLC is currently restricted.
- ICIs can be considered for combination therapy in second- and later-line settings when no other specific treatment options exist.
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