4.4 Article

Next-generation sequencing assisted diagnosis of cervical metastasis in EGFR-mutated lung adenocarcinoma: A case report

Journal

THORACIC CANCER
Volume 12, Issue 19, Pages 2622-2627

Publisher

WILEY
DOI: 10.1111/1759-7714.14143

Keywords

EGFR mutation; metastasis; next-generation sequencing; non-small cell lung cancer; uterine cervix

Funding

  1. Hunan Cancer Hospital Climb Plan [2020QH005]
  2. science and technology innovation Program of Hunan Province [2020SK51110]

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EGFR mutation is common in Asian NSCLC patients, which is the main cause of malignant tumor-related death worldwide. While distant metastases often occur in NSCLC, uterine cervical metastasis is rare. The use of NGS in diagnosing uterine cervical metastasis represents a significant clinical application beyond medication guidance and identification of drug resistance mechanisms.
EGFR mutation has been detected in more than half of non-small cell lung cancer (NSCLC) patients in Asia. Lung cancer is the main cause of malignant tumor-related death worldwide. Although distant metastases often occurs in patients with advanced NSCLC, uterine cervical metastasis is rare. Here, we report a case of EGFR-mutated lung adenocarcinoma with cervical metastasis. A 63-year-old female with known lung adenocarcinoma was found to have abnormal vaginal bleeding during osimertinib follow-up visits. Immunohistochemical (IHC) staining and next-generation sequencing (NGS) of the biopsy sample from the uterine cervical tumor confirmed metastatic dissemination from the primary lung malignancy. NGS assisted the diagnosis of uterine cervical metastasis from the primary lung. This is another major clinical application of NGS in addition to medication guidance and identification of drug resistance mechanisms.

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