TY - JOUR
T1 - Thermal ablation in non-small cell lung cancer
T2 - A review of treatment modalities and the evidence for combination with immune checkpoint inhibitors
AU - Rangamuwa, Kanishka
AU - Leong, Tracy
AU - Weeden, Clare
AU - Asselin-Labat, Marie Liesse
AU - Bozinovski, Steven
AU - Christie, Michael
AU - John, Tom
AU - Antippa, Phillip
AU - Irving, Louis
AU - Steinfort, Daniel
N1 - Publisher Copyright:
© 2021 AME Publishing Company. All rights reserved.
PY - 2021/6
Y1 - 2021/6
N2 - Lung cancer is the leading cause of cancer death worldwide, with approximately 1.6 million cancer related deaths each year. Prognosis is best in patients with early stage disease, though even then five-year survival is only 55% in some groups. Median survival for advanced non-small cell lung cancer (NSCLC) is 8-12 months with conventional treatment. Immune checkpoint inhibitor (ICI) therapy has revolutionised the treatment of NSCLC with significant long-term improvements in survival demonstrated in some patients with advanced NSCLC. However, only a small proportion of patients respond to ICI, suggesting the need for further techniques to harness the potential of ICI therapy. Thermal ablation utilizes the extremes of temperature to cause tumour destruction. Commonly used modalities are radiofrequency ablation (RFA), cryoablation and microwave ablation (MWA). At present thermal ablation is reserved for curative-intent therapy in patients with localized NSCLC who are unable to undergo surgical resection or stereotactic ablative body radiotherapy (SABR). Limited evidence suggests that thermal ablative modalities can upregulate an anticancer immune response in NSCLC. It is postulated that thermal ablation can increase tumour antigen release, which would initiate and upregulated steps in the cancer immunity cycle required to elicit an anticancer immune response. This article will review the current thermal ablative techniques and their ability to modulate an anti-cancer immune response with a view of using thermal ablation in conjunction with ICI therapy.
AB - Lung cancer is the leading cause of cancer death worldwide, with approximately 1.6 million cancer related deaths each year. Prognosis is best in patients with early stage disease, though even then five-year survival is only 55% in some groups. Median survival for advanced non-small cell lung cancer (NSCLC) is 8-12 months with conventional treatment. Immune checkpoint inhibitor (ICI) therapy has revolutionised the treatment of NSCLC with significant long-term improvements in survival demonstrated in some patients with advanced NSCLC. However, only a small proportion of patients respond to ICI, suggesting the need for further techniques to harness the potential of ICI therapy. Thermal ablation utilizes the extremes of temperature to cause tumour destruction. Commonly used modalities are radiofrequency ablation (RFA), cryoablation and microwave ablation (MWA). At present thermal ablation is reserved for curative-intent therapy in patients with localized NSCLC who are unable to undergo surgical resection or stereotactic ablative body radiotherapy (SABR). Limited evidence suggests that thermal ablative modalities can upregulate an anticancer immune response in NSCLC. It is postulated that thermal ablation can increase tumour antigen release, which would initiate and upregulated steps in the cancer immunity cycle required to elicit an anticancer immune response. This article will review the current thermal ablative techniques and their ability to modulate an anti-cancer immune response with a view of using thermal ablation in conjunction with ICI therapy.
KW - Cancer immunity
KW - Immunotherapy
KW - Non-small cell lung cancer (NSCLC)
KW - Thermal ablation
UR - http://www.scopus.com/inward/record.url?scp=85102935365&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85102935365&partnerID=8YFLogxK
U2 - 10.21037/tlcr-20-1075
DO - 10.21037/tlcr-20-1075
M3 - Review article
AN - SCOPUS:85102935365
SN - 2226-4477
VL - 10
SP - 2842
EP - 2857
JO - Translational Lung Cancer Research
JF - Translational Lung Cancer Research
IS - 6
ER -