Worldwide, the leading cause of mortality is lung cancer. There are two most
common types of this cancer: non-small cell lung cancer (NSCLC), which is in first
place in prevalence, and small cell lung cancer (SCLC). Lack of health screening and
nonspecific symptoms are the leading causes of diagnosis in advanced or metastatic
states. Late detection and resistance to therapy are the reasons why the prognosis
remains poor. Lifestyle, environmental factors, and genetic mutations contribute to
the development of lung cancer. The most common proto-oncogene in non-small
cell lung cancer is EGFR. Upon mutation, it becomes an oncogene, which is a
potential therapeutic target. This study aims to review the innovative guidelines for
locally advanced or metastatic NSCLC with EGFR mutations. One of the wellknown
third-generation EGFR tyrosine kinase inhibitors (TKIs) is Osimertinib.
Unfortunately, it quickly developed resistance. There is a significant need to
overcome resistance by combining lazertinib with amivantamab in both first- and
second-line treatments. These drugs work through a different mechanism, allowing
them to attack cancer cells from multiple angles. Studies like Mariposa, Mariposa-2,
Papillon, Chrysalis, and Chrysalis-2 show new therapeutic options for patients with
Locally Advanced or Metastatic NSCLC with EGFR Mutation (Ex20ins, ex19del,
p.L858R). Furthermore, some studies show that reducing amivantamab's side
effects and improving patient comfort can be achieved. There are two opinions: one
is additional dexamethasone premedication, and the second is switching its
administration from intravenous to subcutaneous.
Keywords: lazertinib, amivantamab, lung cancer
