Background
KRAS
, although a common variant of occurrence (~20% of non‐small‐cell lung carcinoma [NSCLC]) has been untargetable, owing to the molecular structure which inherently prevents drug binding.
KRAS
mutations in NSCLC are associated with distinct clinical profiles including smokers and mucinous histology. KRAS G12C mutations account for ~40% KRAS altered NSCLC, but NSCLC being a geographically diverse disease, the features may be distinct in this part of the world. This is a single‐center experience of
KRAS
‐mutated NSCLC including clinical, imaging, pathologic features, and treatment patterns and outcomes.
Methods
This is a single‐center retrospective study of KRAS‐mutated NSCLC. The clinicopathological features and outcomes were retrieved and collated from the medical record archives of the hospital.
Results
Fifty (30.6%) patients with advanced‐stage NSCLC with alterations in the
KRAS
gene were enrolled in the 163 patients who were tested for
KRAS
alterations. The median age was 61 years. Molecular detection revealed three main types of
KRAS
mutations viz‐a‐vis: G12C in 17 (34%), G12V in 9 (18%), and G12D in 6 (12%) patients. Comparing G12C versus the non‐G12C mutated cases, co‐mutations were common in the non‐G12C subgroup (
p
< 0.05). Among the 36, who were treated at our center, all received chemotherapy as the first line with a median progression‐free survival (PFS)of 5.4 months. The PFS of G12C was higher than the non‐G12C subgroup (6.4 vs 3.8 months).
Conclusion
This is the largest single‐center experience from the Indian subcontinent for KRAS‐mutated NSCLC with distinct clinical features. It highlights the unmet need for G12C inhibitors in our country, where prevalence is equivalent to the West.