| Literature DB >> 26348770 |
Maurizio Infante1, Paola Allavena2, Cecilia Garlanda2, Manuela Nebuloni3, Emanuela Morenghi4, Daoud Rahal5, Massimo Roncalli5, Silvio Cavuto6, Samantha Pesce2, Marta Monari2, Serenella Valaperta7, Alessandro Montanelli2, Daniel Solomon8, Edoardo Bottoni1, Valentina Errico1, Emanuele Voulaz1, Manuela Bossi9, Giuseppe Chiesa10, Eliseo Passera10, Alberto Mantovani2,11, Marco Alloisio1.
Abstract
There is a well-established link between inflammation and cancer of various organs, but little data are available on inflammation-associated markers of diagnostic and prognostic clinical utility in pulmonary malignancy. Blood samples were prospectively collected from 75 resectable lung cancer patients before surgery and in a cohort of 1,358 high-risk subjects. Serum levels of long pentraxin 3 (PTX3) were determined by high-sensitivity ELISA. PTX3 immunostaining was evaluated by immunohistochemistry in cancer tissue. Serum PTX3 levels in the high-risk population were not predictive of developing subsequent lung cancer or any other malignancy; however, serum PTX3 values in patients with lung cancer were significantly higher compared with cancer-free heavy smokers. With a cutoff of 4.5 ng/ml, specificity was 0.80, sensitivity 0.69, positive predictive value 0.15 and negative predictive value 0.98. The receiver operating curve (ROC) for serum PTX3 had an area under the curve (AUC) of 83.52%. Preoperative serum PTX3 levels in lung cancer patients did not correlate with patient outcome, but high interstitial expression of PTX3 in resected tumor specimens was a significant independent prognostic factor associated with shorter survival (p < 0.001). These results support the potential of serum PTX3 as a lung cancer biomarker in high-risk subjects. Furthermore, PTX3 immunohistochemistry findings support the role of local inflammatory mechanisms in determining clinical outcome and suggest that local expression of PTX3 may be of prognostic utility in lung cancer patients.Entities:
Keywords: NSCLC; PTX3; biomarker; inflammation
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Year: 2015 PMID: 26348770 DOI: 10.1002/ijc.29822
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396