Advancements in NSCLC Treatment: Efficacy and Mechanisms of Surgery, Targeted Therapy, and Immunotherapy

Authors

  • Jingya Huang

DOI:

https://doi.org/10.62051/wyn27m95

Keywords:

lung cancer; surgery; targeted therapy; immunotherapy.

Abstract

Lung cancer, the most lethal cancer form across the globe, accounts for nearly 1.8 million death each year. The high mortality rate from lung cancer underscores the critical need for effective treatments even in the face of medical progress. Currently available treatment options include radiation therapy, chemotherapy, immunotherapy, targeted therapy, and surgery. This study examines the workings and efficaciousness of the last three treatment in NSCLC. The most effective treatment for early-stage NSCLC continues to be surgical resection, offering high cure rates, especially with procedures like lobectomy and VATS. Targeted therapies have revolutionized treatment by focusing on specific genetic mutations, such as EGFR and ALK. The usage of medications like osimertinib and alectinib has achieved great success. Immunotherapy, which uses immune checkpoint inhibitors like pembrolizumab and nivolumab, has improved the immune system's ability to target cancer cells, opening up new possibilities for long-lasting responses in advanced non-small-cell lung cancer. Notwithstanding these developments, problems including immunological-related side effects and medication resistance still exist. The present status of these medicines, their modes of action, and their effects on patient outcomes are highlighted in this paper.

Downloads

Download data is not yet available.

References

[1] J.R. Brahmer, S.S. Tykodi, L.Q. Chow, W.J. Hwu, S.L. Topalian, P. Hwu, ... J.D. Powderly, Safety and activity of anti-PD-L1 antibody in patients with advanced cancer, New England Journal of Medicine. 366 (2012) 2455-2465. doi:10.1056/NEJMoa1200694.

[2] American Cancer Society. (2020). Cancer facts & figures 2020. Information on https://www.cancer.org/research/ cancer-facts-statistics/all-cancer-facts-figures/cancer-facts-figures-2020.html

[3] National Cancer Institute. (n.d.). Lung cancer—patient version. Information on https://www.cancer.gov/types/lung

[4] R.L. Siegel, K.D. Miller, A. Jemal, Cancer statistics, 2020, CA: A Cancer Journal for Clinicians. 70 (2020) 7-30. doi:10.3322/caac.21590.

[5] N. Normanno, C. De Luca, A. Maiello, S. Campiglio, S. Napolitano, S. Mancino, G. Carotenuto, M. Agrawal, A. Halmos, L. Rosell, Epidermal growth factor receptor (EGFR) signaling in cancer, Gene. 366 (2006) 2-16.

[6] J.C. Soria, G.J. Kim, J.J. Wu, Osimertinib in Untreated EGFR-Mutated Advanced Non-Small-Cell Lung Cancer, New England Journal of Medicine. 378 (2018) 113-125.

[7] T. Reungwetwattana, T.S. Mok, L. Spigel, Central nervous system response to osimertinib in patients with T790M-positive advanced non-small-cell lung cancer: pooled data from two Phase II studies, Journal of Clinical Oncology. 36 (2018) 1542-1550.

[8] B. Hallberg, R.H. Palmer, Mechanistic insight into ALK receptor tyrosine kinase in human cancer biology, Nature Reviews Cancer. 13 (2013) 685-700.

[9] J.C. Soria, H. Tan, E. Chiari, Alectinib versus Crizotinib in Untreated ALK-Positive Non–Small-Cell Lung Cancer, New England Journal of Medicine. 377 (2017) 829-838.

[10] J. Zhao, Q. Lin, Y. Song, D. Liu, Universal CARs, universal T cells, and universal CAR T cells, Journal of Hematology & Oncology. 12 (2019) 1-9.

[11] K. Newick, S. O'Brien, E. Moon, S.M. Albelda, CAR T cell therapy for solid tumors, Annual Review of Medicine. 68 (2017) 139-152.

[12] S.V. Sharma, D.W. Bell, J. Settleman, D.A. Haber, Epidermal growth factor receptor mutations in lung cancer, Nature Reviews Cancer. 7 (2007) 169-181. doi:10.1038/nrc2088.

[13] Revolutionizing Gene Editing with CRISPR Cas9, information on https://lifesciences.danaher.com/us/en/library/ crispr-cas9.html

Downloads

Published

24-12-2024

How to Cite

Huang, J. (2024). Advancements in NSCLC Treatment: Efficacy and Mechanisms of Surgery, Targeted Therapy, and Immunotherapy. Transactions on Materials, Biotechnology and Life Sciences, 7, 27-32. https://doi.org/10.62051/wyn27m95