Targeted Therapy for Cancers: From Ongoing Clinical Trials to FDA-Approved Drugs.
Ha Yeong ChoiJi-Eun ChangPublished in: International journal of molecular sciences (2023)
The development of targeted therapies has revolutionized cancer treatment, offering improved efficacy with reduced side effects compared with traditional chemotherapy. This review highlights the current landscape of targeted therapy in lung cancer, colorectal cancer, and prostate cancer, focusing on key molecular targets. Moreover, it aligns with US Food and Drug Administration (FDA)-approved drugs and drug candidates. In lung cancer, mutations in the epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) gene rearrangements have emerged as significant targets. FDA-approved drugs like osimertinib and crizotinib specifically inhibit these aberrant pathways, providing remarkable benefits in patients with EGFR-mutated or ALK-positive lung cancer. Colorectal cancer treatment has been shaped by targeting the vascular endothelial growth factor (VEGF) and EGFR. Bevacizumab and cetuximab are prominent FDA-approved agents that hinder VEGF and EGFR signaling, significantly enhancing outcomes in metastatic colorectal cancer patients. In prostate cancer, androgen receptor (AR) targeting is pivotal. Drugs like enzalutamide, apalutamide, and darolutamide effectively inhibit AR signaling, demonstrating efficacy in castration-resistant prostate cancer. This review further highlights promising targets like mesenchymal-epithelial transition (MET), ROS1, BRAF, and poly(ADP-ribose) polymeras (PARP) in specific cancer subsets, along with ongoing clinical trials that continue to shape the future of targeted therapy.
Keyphrases
- epidermal growth factor receptor
- drug administration
- advanced non small cell lung cancer
- tyrosine kinase
- vascular endothelial growth factor
- prostate cancer
- clinical trial
- small cell lung cancer
- radical prostatectomy
- endothelial cells
- dna damage
- metastatic colorectal cancer
- squamous cell carcinoma
- locally advanced
- cancer therapy
- gene expression
- wild type
- genome wide
- phase iii
- diffuse large b cell lymphoma
- study protocol
- metabolic syndrome
- young adults
- randomized controlled trial
- adipose tissue
- adverse drug
- reactive oxygen species
- climate change
- risk assessment
- rectal cancer
- protein kinase
- peripheral blood
- lymph node metastasis