Associations Between Mutations and Histologic Patterns of Mucin in Lung Adenocarcinoma Invasive Mucinous Pattern and Extracellular Mucin Are Associated With KRAS Mutation

被引:140
作者
Kadota, Kyuichi [1 ,3 ,6 ]
Yeh, Yi-Chen [1 ]
D'Angelo, Sandra P. [2 ]
Moreira, Andre L. [3 ]
Kuk, Deborah [4 ]
Sima, Camelia S. [4 ]
Riely, Gregory J. [2 ]
Arcila, Maria E. [3 ]
Kris, Mark G. [2 ]
Rusch, Valerie W. [1 ]
Adusumilli, Prasad S. [1 ,5 ]
Travis, William D. [3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Surg, Div Thorac Serv, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med, Thorac Oncol Serv, Div Solid Tumor Oncol, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10065 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY 10065 USA
[5] Mem Sloan Kettering Canc Ctr, Ctr Cell Engn, New York, NY 10065 USA
[6] Kagawa Univ, Fac Med, Dept Diagnost Pathol, Takamatsu, Kagawa 760, Japan
关键词
lung; adenocarcinoma; subtype; mutation; mucin; GROWTH-FACTOR RECEPTOR; BRONCHIOLOALVEOLAR PATHOLOGICAL SUBTYPE; ATYPICAL ADENOMATOUS HYPERPLASIA; EGFR MUTATIONS; GENE-MUTATIONS; CLINICOPATHOLOGICAL FEATURES; INTERNATIONAL-ASSOCIATION; ROUTINE-PRACTICE; GRADING SYSTEM; BRAF MUTATIONS;
D O I
10.1097/PAS.0000000000000246
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Multiple reports indicate that epidermal growth factor receptor (EGFR) mutations are associated with lepidic-pattern lung adenocarcinoma and that KRAS mutations are associated with invasive mucinous adenocarcinoma. We sought to investigate the association between EGFR and KRAS mutations and specific morphologic characteristics, such as predominant histologic subtype and mucinous features. Clinical data for 864 patients with resected lung adenocarcinoma that underwent molecular testing for EGFR and KRAS mutations were collected. Histologic subtyping was performed according to the IASLC/ATS/ERS lung adenocarcinoma classification, with attention given to signet-ring cell feature and extracellular mucin. EGFR mutations were detected using a polymerase chain reaction-based sizing assay, KRAS mutations were detected using Sanger sequencing, and ALK expression was detected using immunohistochemistry. Invasive mucinous adenocarcinoma was associated with KRAS mutation (P<0.001). Among invasive mucinous adenocarcinomas with KRAS mutation, a pure mucinous pattern was more common than a mixed mucinous/nonmucinous pattern (P=0.002). Invasive mucinous adenocarcinoma was associated with KRAS transition mutations (G -> A) but not transversion mutations (G -> T or G -> C) compared with nonmucinous tumors (P=0.009). The lepidic-predominant group was associated with EGFR mutation compared with nonlepidic-predominant tumors (P=0.011). Extracellular mucin was associated with KRAS mutation (P<0.001), whereas signet-ring cell feature was not associated with EGFR or KRAS mutation (P=0.517). ALK expression was associated with signet-ring cell feature (P=0.001) but not with extracellular mucin (P=0.089). Our study shows that histologic patterns of mucin in lung adenocarcinoma-including invasive mucinous adenocarcinoma and extracellular mucin-are associated with KRAS mutation.
引用
收藏
页码:1118 / 1127
页数:10
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