Targeted Therapy Management in NSCLC Patients Using Cytology: Experience from a Tertiary Care Cancer Center
Vidya H Veldore1, Shekar Patil2, Shilpa Prabhudesai3
1Triesta Reference Laboratory, Triesta Sciences, A Unit of Health Care Global Enterprises Ltd., 8, P Kalinga Rao Road, HCG Tower 1, SR Nagar, Bangalore, 560 027, India. vidya.veldore@gmail.com.
Cytological samples effectively screen for epidermal growth factor receptor (EGFR) mutations in non-small cell lung cancer (NSCLC). This molecular testing aids in directing patient treatment, showing high mutation detection rates.
Area of Science:
- Oncology
- Molecular Diagnostics
- Pathology
Background:
- Cytological material is increasingly utilized for molecular testing in various cancers, complementing traditional biopsy methods.
- This study focuses on the application of cytological samples for diagnosing non-small cell lung cancer (NSCLC).
Purpose of the Study:
- To evaluate the efficacy of using cytological material for screening epidermal growth factor receptor (EGFR) mutations in NSCLC patients.
- To share institutional experience in molecular testing of cytological specimens for NSCLC.
Main Methods:
- Screening of fine needle aspirates, pleural effusions, and cell blocks from 223 NSCLC patients with suspected malignancy.
- Utilized Scorpion(®) ARMS real-time polymerase chain reaction (PCR) technology to detect EGFR mutations in exons 18-21.
Main Results:
- Epidermal growth factor receptor (EGFR) mutations were detected in 43.5% of the analyzed cytological samples.
- Exon 19 deletions were the most frequent EGFR mutation (27.2%), followed by exon 21 (15.5%).
- A significant correlation was observed between mutation status and sex, with a higher prevalence in women.
Conclusions:
- Cytological material is a viable and effective source for molecular testing in a subset of non-small cell lung cancer (NSCLC) patients.
- This approach facilitates personalized treatment strategies by identifying actionable EGFR mutations.
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