Comprehensive Histologic Assessment Helps to Differentiate Multiple Lung Primary Nonsmall Cell Carcinomas From Metastases

The pathologic classification of nonsmall cell lung cancer (NSCLC) is evolving. Lung adenocarcinoma is morphologically heterogeneous, with mixtures of acinar, papillary, bronchioloalveolar, and solid patterns in more than 80% of cases. In case of synchronous or metachronous multiple NSCLC, the distinction of intrapulmonary metastases from independent primary tumors is of great clinical importance as it influences staging and potentially the therapeutic strategy. Here we took advantage of a cohort of 20 patients with 42 multiple NSCLC tumors (24 potential pair comparisons) that were annotated molecularly using genomic and mutational profiling to evaluate the value of comprehensive histologic assessment in this setting. Using the Martini-Melamed criteria, paired tumors were characterized as multiple primary NSCLCs in 21 cases and as intrapulmonary metastases in 3 cases. Genomic and mutational data led to a diagnosis of multiple primaries in 14 cases and of metastases in 8 cases; 2 cases could not be assessed. This molecular characterization contradicted the Martini-Melamed diagnosis in 7 (32%) of the 22 assessable comparisons. Adenocarcinoma was found in 32 (76%) of the 42 tumors. After review in a blinded fashion, semiquantitative comprehensive histologic assessment of paired tumors was different in 16 and similar in 8 paired tumors. We found that comparing adenocarcinomas is a complex issue that requires assessment not only of percentages of the histologic subtypes, but also the recording of additional histologic details such as cytologic features, patterns of stroma, necrosis, discrete nodularity versus miliary growth and variants such as clear cell, signet ring, mucinous, and fetal patterns. We also found that paired squamous cell carcinomas could be compared based on histologic subtyping in addition to cytologic and stromal characteristics. Considering histologically different tumors as multiple primaries, and similar tumors as metastases, comprehensive histologic subtyping was consistent with the molecular characterization in 20 (91%) of the 22 pairs comparisons. In summary, based on a well characterized cohort with detailed clinical, pathologic and molecular data, we found comprehensive histologic assessment is a powerful tool that seems to be a promising way to determine whether multiple lung adenocarcinomas or squamous cell carcinomas are metastatic or multiple primaries. This has great clinical implications for staging and therapeutic management of lung cancer patients with multiple tumors. Given its high correlation with molecular characterization of such tumors, it may provide a much cheaper and faster method to address this problem.

[1]  C. R. Leemans,et al.  Second primary tumors and field cancerization in oral and oropharyngeal cancer: molecular techniques provide new insights and definitions. , 2002, Head & neck.

[2]  T. Nagayasu,et al.  Different epidermal growth factor receptor gene mutations in a patient with 2 synchronous lung cancers. , 2007, Clinical lung cancer.

[3]  A. Sabichi,et al.  The risk of second primary tumors after resection of stage I nonsmall cell lung cancer. , 2003, The Annals of thoracic surgery.

[4]  Brian H. Dunford-Shore,et al.  Somatic mutations affect key pathways in lung adenocarcinoma , 2008, Nature.

[5]  Derek Y. Chiang,et al.  Characterizing the cancer genome in lung adenocarcinoma , 2007, Nature.

[6]  E. Gabrielson Worldwide trends in lung cancer pathology , 2006, Respirology.

[7]  N. Girard,et al.  Genomic and Mutational Profiling to Assess Clonal Relationships Between Multiple Non–Small Cell Lung Cancers , 2009, Clinical Cancer Research.

[8]  T. Fabian Multiple primary lung cancers. , 2018, Journal of thoracic disease.

[9]  A. Cazes,et al.  Multiple lung cancers prognosis: what about histology? , 2008, The Annals of thoracic surgery.

[10]  W. Gerald,et al.  Lung Adenocarcinoma: Modification of the 2004 WHO Mixed Subtype to Include the Major Histologic Subtype Suggests Correlations Between Papillary and Micropapillary Adenocarcinoma Subtypes, EGFR Mutations and Gene Expression Analysis , 2008, The American journal of surgical pathology.

[11]  P. V. van Diest,et al.  Comparative genomic hybridisation as a supportive tool in diagnostic pathology , 2003, Journal of clinical pathology.

[12]  Yuki Togashi,et al.  EML4-ALK Fusion Is Linked to Histological Characteristics in a Subset of Lung Cancers , 2008, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

[13]  R. Wilson,et al.  EGF receptor gene mutations are common in lung cancers from "never smokers" and are associated with sensitivity of tumors to gefitinib and erlotinib. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[14]  Irina Ostrovnaya,et al.  A metastasis or a second independent cancer? Evaluating the clonal origin of tumors using array copy number data , 2010, Statistics in medicine.

[15]  Pascal Thomas,et al.  Synchronous multiple primary lung cancer: an increasing clinical occurrence requiring multidisciplinary management. , 2007, The Journal of thoracic and cardiovascular surgery.

[16]  E. Brambilla,et al.  Lung carcinomas with a basaloid pattern: a study of 90 cases focusing on their poor prognosis , 2008, European Respiratory Journal.

[17]  WHO histological classification of tumours of the vulva , 2011 .

[18]  Y. Ishikawa,et al.  Early-Stage Lung Adenocarcinomas With a Micropapillary Pattern, a Distinct Pathologic Marker for a Significantly Poor Prognosis , 2003, The American journal of surgical pathology.

[19]  The World Health Organization. Histological typing of lung tumours. , 1982, Neoplasma.

[20]  E. Ruffini,et al.  The significance of intrapulmonary metastasis in non-small cell lung cancer: upstaging or downstaging? A re-appraisal for the next TNM staging system. , 2008, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.