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Precision Medicine in Treating Lung Cancer: A Narrative Review on Treatments Targeting Oncogenic Genetic Mutations
Eesha Chitneni1, Adwaith Venugopal2, Confidence Obianuju Okorie3
1Medicine, MediCiti Institute of Medical Sciences, Hyderabad, IND.
Abstract:
Lung cancer is among the leading causes of cancer-related mortality worldwide. It is classified into small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC), with NSCLC being more prevalent. There have been advancements in managing extensive research on immunotherapy agents, oncolytic viruses, and targeted therapies by understanding the genetic mutations and molecular mechanisms behind lung cancer. Targeted therapy is the new paradigm in the treatment of lung cancer, especially NSCLC, and the aim is to inhibit specific proteins involved in cancer growth and progression. They primarily utilize small molecule inhibitors, monoclonal antibodies (mAbs), and antibody-drug conjugates (ADCs) to attack specific oncogenic driver mutations such as epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK), Kirsten rat sarcoma viral oncogene homolog (KRAS), c-ros oncogene 1 (ROS1), and immune checkpoint pathways. These agents have improved outcomes and have shown efficacy in clinical trials, making them a preferred option over traditional chemotherapy. However, the associated adverse effects of these agents, along with drug resistance, remain a challenge. In this review, we discuss targeted therapies for lung cancer, their efficacy, clinical trials, adverse effects, mechanisms of resistance, and future directions.
Insights
Targeted therapy offers a new approach to treating non-small cell lung cancer (NSCLC) by inhibiting specific mutations. While effective, challenges like adverse effects and drug resistance require further research.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Lung cancer is a leading cause of cancer mortality globally.
- Non-small cell lung cancer (NSCLC) is the most common type.
- Advancements in understanding genetic mutations drive new lung cancer treatments.
Purpose of the Study:
- To review targeted therapies for lung cancer, focusing on NSCLC.
- To discuss the efficacy, clinical trials, and adverse effects of these therapies.
- To explore mechanisms of drug resistance and future research directions.
Main Methods:
- Review of current literature on targeted lung cancer therapies.
- Analysis of small molecule inhibitors, monoclonal antibodies (mAbs), and antibody-drug conjugates (ADCs).
- Examination of targeted mutations including EGFR, ALK, KRAS, and ROS1.
Main Results:
- Targeted therapies have improved outcomes in lung cancer clinical trials.
- These agents target specific oncogenic driver mutations and immune checkpoints.
- Adverse effects and the development of drug resistance are significant challenges.
Conclusions:
- Targeted therapy is a preferred treatment option for NSCLC over traditional chemotherapy.
- Further research is needed to overcome resistance and manage adverse effects.
- Understanding molecular mechanisms is key to advancing lung cancer treatment.
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