PIK3CA mutation as a distinctive genetic feature of non-small cell lung cancer with chronic obstructive pulmonary disease: A comprehensive mutational analysis from a multi-institutional cohort. (October 2017)

• Record Type: Journal Article
• Authors: Sawa, Kenji; Koh, Yasuhiro; Kawaguchi, Tomoya; Kambayashi, Satoshi; Asai, Kazuhisa; Mitsuoka, Shigeki; Kimura, Tatsuo; Yoshimura, Naruo; Yoshimoto, Naoki; Kubo, Akihito; Saka, Hideo; Matsumura, Akihide; Wanibuchi, Hideki; Yamamoto, Nobuyuki; Nishiyama, Noritoshi; Hirata, Kazuto
• Is Part Of: Lung cancer. Volume 112(2017)
• Page Start: 96
• Page End: 101
• Publication Date: 2017-10
• Subjects: Non-small cell lung cancer -- Chronic obstructive pulmonary disease -- PIK3CA -- Nrf2 -- Next generation sequence; Lungs -- Cancer -- Periodicals; Lung Neoplasms -- Abstracts; Lung Neoplasms -- Periodicals; Poumons -- Cancer -- Périodiques; Lungs -- Cancer; Periodicals; Electronic journals; Electronic journals; 616.99424
• DOI: 10.1016/j.lungcan.2017.07.039
• Languages: English
• ISSNs: 0169-5002

Abstract

Highlights: A mutual developmental mechanism between NSCLC and COPD has been proposed. Molecular analysis of 197 resected NSCLC was performed by next generation sequencing. The frequency of PIK3CA mutation increased in parallel with the COPD severity. PIK3CA mutation was distinctive genetic features of NSCLC with COPD. Abstract: Objectives: Non-small cell lung cancer (NSCLC) and chronic obstructive pulmonary disease (COPD) have been proposed to have a mutual developmental mechanism, but their association has not been fully understood. We aimed to examine the association of the mutational landscape of NSCLC with co-morbid COPD. Materials and methods: A total of 197 surgical specimens of early stage NSCLC were retrospectively collected from two independent sources, namely, the Japan Molecular Epidemiology for Lung Cancer Study and the Osaka City University Hospital cohort from 2010 to 2013. COPD and its severity were defined by the Global Initiative for Chronic Obstructive Lung Disease (GOLD) guidelines and grading system. For molecular profiling of NSCLC patients with COPD, the extracted DNAs were deep-sequenced using next generation sequence technologies for somatic mutations in a maximum 72 cancer-associated genes. Logistic regression analysis was performed to evaluate the impact of COPD on the somatic mutations. Results: The COPD group (n = 77), including 56 GOLD 1 and 21 GOLD 2 or 3 patients, had 58 squamous cell lung carcinoma (SCC) cases and 19 adenocarcinoma cases. The non-COPD group (n = 120) had 53 SCC cases, 64 adenocarcinoma cases, and three cases with other histology. The frequency of PIK3CA mutation was significantly higher in the COPD group than in the non-COPD group (10.4% vs. 1.7%, p = 0.015). Meanwhile, NFE2L2 mutation was observed only in SCC cases, with no difference in the frequency between the two groups (17.2% vs. 17.0%). In the multivariate logistic regression model with consideration for COPD status, age, smoking dose, pathological stage, and histology, significantly more PIK3CA mutation was observed in the presence of COPD (odds ratio = 5.31, 95% CI: 1.03–27.29, p = 0.046). Conclusions: PIK3CA mutation is a distinctive genetic feature of NSCLC with COPD, regardless of age, smoking dose, pathological stage, and histology.