The importance of EGFR mutation testing in squamous cell carcinoma or non-small cell carcinoma favor squamous cell carcinoma diagnosed from small lung biopsies

被引:15
|
作者
Ho, Hsiang-Ling [1 ,2 ]
Kao, Hua-Lin [1 ,3 ,4 ]
Yeh, Yi-Chen [1 ]
Chou, Teh-Ying [1 ,2 ,3 ]
机构
[1] Taipei Vet Gen Hosp, Dept Pathol & Lab Med, Div Mol Pathol, Taipei, Taiwan
[2] Natl Yang Ming Univ, Lab Sci Med, Dept Biotechnol & Lab Sci Med, Taipei, Taiwan
[3] Natl Yang Ming Univ, Inst Clin Med, Taipei, Taiwan
[4] Taipei Med Univ Hosp, Dept Pathol, Taipei, Taiwan
关键词
Lung cancer; EGFR mutation; Squamous cell carcinoma; Adenosquamous carcinoma; Small biopsy; GROWTH-FACTOR RECEPTOR; TYROSINE KINASE INHIBITORS; ADENOSQUAMOUS CARCINOMA; CHINESE PATIENTS; CANCER; GEFITINIB; CLASSIFICATION; EFFICACY; ADENOCARCINOMAS; ASSOCIATION;
D O I
10.1186/s13000-019-0840-2
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
BackgroundAdenosquamous carcinoma (ADSC) of the lung, a rare but aggressive subtype of non-small cell lung cancer (NSCLC), is defined as a carcinoma containing components of adenocarcinoma (ADC) and squamous cell carcinoma (SqCC). Mutations of epidermal growth factor receptor (EGFR) are found at a frequency of 15 to 44% in Asian ADSC, and EGFR tyrosine kinase inhibitors (EGFR-TKIs) are a more effective treatment for EGFR-mutated ADSC compared to chemotherapy. However, ADSC in small lung biopsies could be misdiagnosed as SqCC or non-small cell carcinoma (NSCC) favor SqCC due to undersampling, which may result in neglecting of EGFR mutation testing and affecting patients' clinical management, particularly in Asian patients that relatively have high prevalence of EGFR mutation.MethodsA total of 148 small lung biopsy cases with pathological diagnosis of SqCC or NSCC favor SqCC were retrospectively enrolled. The frequency of EGFR mutations and the correlation between patients' EGFR mutation status and clinicopathological characteristics were evaluated.ResultsEGFR mutations were found in 8.8% (13 /148) of all cases with 5.2% (7/135) in SqCC and 46.2% (6/13) in NSCC favor SqCC. There were 7 (53.8%) L858R mutation, 4 (30.8%) exon 19 deletions, and 2 (15.4%) cases with coexistent L858R and T790M mutations. Multivariate analysis showed that EGFR mutations were more prevalent in never-smokers (83.3% versus 16.7%, p=0.006) and patients diagnosed as NSCC favor SqCC (46.2% versus 5.2%, p=0.001). Moreover, 75% (3/4) of EGFR mutation-positive cases with subsequent surgical resection or rebiopsy were further diagnosed as ADSC.ConclusionsEGFR mutation testing should be performed in Asian patients with SqCC diagnosed from small lung biopsies, especially in never-smokers and patients with diagnosis of NSCC favor SqCC, which have a high probability of being ADSC.
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页数:8
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