Cancer Res Treat.  2019 Jan;51(1):158-168. 10.4143/crt.2018.084.

Impact of Pulmonary Tuberculosis on the EGFR Mutational Status and Clinical Outcome in Patients with Lung Adenocarcinoma

Affiliations
  • 1Division of Pulmonary Medicine, Department of Internal Medicine, Dongnam Institute of Radiological & Medical Sciences, Busan, Korea.
  • 2Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Kyung Hee University School of Medicine, Seoul, Korea. humanmd04@hanmail.net

Abstract

PURPOSE
Although it has been suggested that pulmonary tuberculosis (TB) is associated with increased risk of lung cancer, the exact mechanism is not clearly identified. We investigated the effect of pulmonary TB on the epidermal growth factor receptor (EGFR) mutational status and clinical outcome in patients with pulmonary adenocarcinoma.
MATERIALS AND METHODS
We reviewed data of patients diagnosed with pulmonary adenocarcinoma harboring EGFR mutations and treated at our institution from 2008 to 2015. We divided our population into two groups: patients with pre-existing TB lesions on chest computed tomography scan (TB group) and those without the lesions (non-TB group). We compared the differences in EGFR mutational status, response to tyrosine kinase inhibitors (TKIs) and survival between the two groups.
RESULTS
A total of 477 patients with pulmonary adenocarcinoma were analyzed. One hundred eighty-three patients (39%) had EGFR-mutated tumors and 100 (21%) patients had pre-existing TB lesions. The frequency of EGFR mutation was significantly higher in the TB group compared with the non-TB group (56% vs. 34%, p=0.038). Pre-existing TB lesions were independently associated with more frequent EGFR mutations in multivariate analysis (odds ratio, 1.43). In addition, both the progression-free survival (9.1 months vs. 11.6 months, p=0.020) and the overall survival (19.4 months vs. 24.5 months, p=0.014) after first-line EGFR-TKIs were significantly shorter in the TB group than in the non-TB group.
CONCLUSION
Previous pulmonary TB may be associated with more frequent EGFR mutations and poorer treatment response to EGFR-TKIs in patients with pulmonary adenocarcinoma.

Keyword

Lung neoplasms; Adenocarcinoma; Tuberculosis; Epidermal growth factor receptor; Mutation; Tyrosine kinase inhibitors; Response

MeSH Terms

Adenocarcinoma*
Disease-Free Survival
Humans
Lung Neoplasms
Lung*
Multivariate Analysis
Protein-Tyrosine Kinases
Receptor, Epidermal Growth Factor
Thorax
Tuberculosis
Tuberculosis, Pulmonary*
Protein-Tyrosine Kinases
Receptor, Epidermal Growth Factor

Figure

  • Fig. 1. Kaplan-Meier survival curves for progression-free survival (A) and overall survival (B) in patients treated with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors for EGFR-mutated lung adenocarcinoma. p-values were determined using the log-rank test. PFS, progression-free survival; OS, overall survival; TB, tuberculosis.


Reference

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