Prognostic impact and clinicopathological correlations of the cribriform pattern in pulmonary adenocarcinoma

A novel classification of pulmonary adenocarcinoma (ADC) distinguishing five growth patterns has been established by the International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society. There is evidence that an additional cribriform pattern associates w...

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Hauptverfasser: Warth, Arne (VerfasserIn) , Muley, Thomas (VerfasserIn) , Kossakowski, Claudia (VerfasserIn) , Stenzinger, Albrecht (VerfasserIn) , Schirmacher, Peter (VerfasserIn) , Dienemann, Hendrik (VerfasserIn) , Weichert, Wilko (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 20 November 2015
In: Journal of thoracic oncology
Year: 2015, Jahrgang: 10, Heft: 4, Pages: 638-644
ISSN:1556-1380
DOI:10.1097/JTO.0000000000000490
Online-Zugang:Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1097/JTO.0000000000000490
Verlag, kostenfrei, Volltext: http://www.sciencedirect.com/science/article/pii/S1556086415323662
Volltext
Verfasserangaben:Arne Warth, Thomas Muley, Claudia Kossakowski, Albrecht Stenzinger, Peter Schirmacher, Hendrik Dienemann, and Wilko Weichert

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520 |a A novel classification of pulmonary adenocarcinoma (ADC) distinguishing five growth patterns has been established by the International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society. There is evidence that an additional cribriform pattern associates with a distinct clinical behavior. We evaluated the predominant growth pattern of 674 resected ADC as recommended by the International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society, including the cribriform pattern. The predominant pattern type was correlated with clinical, molecular, and survival data. Two hundred forty-eight (36.8%) of the pulmonary ADC were solid, 207 (30.6%) were acinar, 101 (15%) were papillary, 55 (8.2%) were micropapillary, 35 (5.2%) were lepidic, and 28 cases (4.2%) were cribriform predominant (cpADC). Minor cribriform components were frequently observed (28.6% of all cases). cpADC showed the second highest proliferative capacity of all patterns, no somatic mutations in the epidermal growth factor receptor (p = 0.001) and a high rate of KRAS mutations. Overall survival (OS) of patients with cpADC (mean OS: 62.7 months) ranged in between survival times of patients with acinar (mean OS: 71.3 months) and solid predominant ADC (mean OS: 54.5 months); cpADC was associated with the worst disease-free survival (DFS) of all patterns (mean DFS: 36.9 months). Both associations were confirmed by multivariate analysis (p < 0.01 for both OS and DFS). Hazard ratios for cpADC were 1.72 for OS and 2.99 for DFS, with lepidic predominant ADC set as reference (hazard ratio: 1). Our data support the introduction of cpADC as a novel category into future morphology based on pulmonary ADC classifications. Further international studies are required to validate the reported clinicopathological associations of the cribriform pattern. 
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