dc.description.abstract | Background: Currently, the development of lung cancer therapy has entered the
era of targeted therapy based on its molecular profile, where smoking-associated
malignancies show a varied and interrelated genomic mutation profile. KRAS
mutations and TP53 mutations are mutations that occur in smoking-related lung
cancer and affect the low rate of therapeutic success and survival of lung cancer
patients. This study aims to assess the role of KRAS and TP53 mutations as
prognostic factors for lung cancer
Methods: This study is a retrospective cohort study conducted in 2020-2021 and involved
107 subjects with certain inclusion and exclusion criteria. However, only 52 paraffin blocks
from bronchoscopy, Trans Thoracal Lung Biopsy (TTLB), and open surgery procedures
were successfully extracted using the FFPE Quick-DNA mini preparation. KRAS gene and
TP53 gene were amplified using PCR with specific primers for exon 2 (KRAS) and exon 5-
9 (TP53). Sequencing analysis was performed using Unipro Ugene software and compared
with reference sequences. Protein base changes were then analyzed by BLASTn
application. All clinical characteristics were obtained from medical records. The patient's
prognosis was assessed for overall survival (OS) and progression free survival (PFS) by
survival analysis with Kaplan Meier and Logrank analysis to assess the associations
between OS and PFS with TP53 and KRAS mutations.
Results: The majority of the subjects were men with the age of more than 60 years, heavy smokers,
with adenocarcinoma lung cancer. KRAS mutations were not detected in all study subjects. TP53
mutations were detected in 5 subjects at exons 5, 6, and 8. During the analysis, it was seen that the
median OS of patients with TP53 mutations was 7 months while those without mutations was 9 months.
Meanwhile, the median PFS of patients with TP53 mutations was 3 months while those without
mutations was 6 months. In statistical tests, there is no associations between TP53 mutations and OS
and PFS of lung cancer patients with p-value > 0.05
Conclusion: TP53 and KRAS mutations do not have a significant effect on the
prognosis of lung cancer patients. | en_US |