Small-Cell Carcinoma With an Epidermal Growth Factor Receptor Mutation in a Never-Smoker With Gefitinib-Responsive Adenocarcinoma of the Lung

被引:46
作者
Alam, Naheed [1 ]
Gustafson, Karen S. [3 ]
Ladanyi, Marc [4 ]
Zakowski, Maureen F. [4 ]
Kapoor, Atul [1 ]
Truskinovsky, Alexander M. [2 ]
Dudek, Arkadiusz Z. [1 ]
机构
[1] Univ Minnesota, Div Hematol Oncol & Transplantat, Sch Med, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Lab Med & Pathol, Sch Med, Minneapolis, MN 55455 USA
[3] Fox Chase Canc Ctr, Dept Pathol, Philadelphia, PA 19111 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
关键词
EGFR mutation; L858R; LREA; Polymerase chain reaction; GENE-MUTATIONS; EGFR MUTATION; CANCERS; FEATURES;
D O I
10.3816/CLC.2010.n.046
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Activating mutations in the epidermal growth factor receptor (EGFR) gene are extremely rare in small-cell lung cancer (SCLC). Here, we present a case of an EGFR-mutant gefitinib-responsive non-small-cell lung cancer (NSCLC) of adenocarcinoma histology occurring in a never-smoker followed by subsequent diagnosis of metastatic SCLC carrying an EGFR mutation. Although gefitinib therapy of the primary NSCLC resulted in disease control for over 3 years, the patient subsequently developed metastatic SCLC to the liver. Epidermal growth factor receptor mutation analysis revealed that the exon 21 L858R activating mutation was present in both the original lung adenocarcinoma and the metastatic SCLC. We hypothesize that SCLC either evolved from the previously diagnosed NSCLC or that both arose from a common precursor. Further comparative molecular analysis of these histologically distinct tumors would be of value to better understand the potential role of EGFR in the pathogenesis of SCLC in never-smokers, and the role of selection for an EGFR-mutant SCLC subclone as an unusual mechanism of acquired resistance to EGFR inhibitors in NSCLC.
引用
收藏
页码:E1 / E4
页数:4
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