Metropolis Healthcare conducted a landmark seven-year study (2015-2021) analyzing the clinicopathological and molecular features of over 3,200 lung cancer patients. The study focused on genetic alterations in key genes like Epidermal Growth Factor Receptor (EGFR), Anaplastic Lymphoma Kinase (ALK), and c-ros oncogene 1 (ROS1), which are pivotal in non-small cell lung cancer (NSCLC) development. Molecular profiling of these markers is revolutionizing cancer care by enabling targeted therapies tailored to patients’ genetic profiles.
The study highlighted next-generation sequencing (NGS) as a critical tool for identifying lung cancer cases and uncovering actionable molecular targets, leading to expanded treatment options. Among the analyzed samples, 83% were adenocarcinomas (a common NSCLC type), while 17% were squamous cell carcinomas, primarily seen in patients over 60. The findings emphasized the importance of molecular diagnostics in guiding personalized treatment strategies.
Dr. Kirti Chadha, chief scientific and innovation officer at Metropolis Healthcare, stressed the value of genetic profiling in selecting the most effective treatments. "Detailed molecular analysis enables clinicians to tailor therapies to a patient’s genetic profile, significantly improving treatment outcomes in NSCLC care,” she noted.
The study aligns with evolving global standards in molecular diagnostics, such as the 2023 ESMO guidelines, which recommend a broader range of biomarkers, including BRAF, RET, MET, NTRK, HER2, and KRAS G12C. These advances build on the 2017 NCCN guidelines, which emphasized ALK, ROS1, and EGFR mutations. By incorporating comprehensive 50-gene panels, Metropolis Healthcare is expanding its mutation detection capabilities, reinforcing its commitment to precision medicine and improving lung cancer outcomes through advanced molecular profiling.