Lung cancer diagnosis via breath analysis has to overcome some issues that can be summarized by two crucial points: (1) further developments for more performant breath sampling technologies; (2) discovering more differentiated volatile fingerprints to be ascribed to specific altered biological mechanisms. The present work merges these two aspects in a pilot study, where a breath volume, sampled via endoscopic probe, is analyzed by an array of non-selective gas sensors. Even if the original non-invasive methods of breath analysis has been laid in favour of the endoscopic means, the innovative technique here proposed allows the analysis of the volatile mixtures directly sampled near the tumor mass. This strategy could open the way for a better understanding of the already obtained discrimination among positive and negative cancer cases. The results obtained so far confirm the established discrimination capacity. This allows to discriminate the different subtypes of lung cancer with 75% of correct classification between adenocarcinoma and squamous cell carcinoma. This result suggests that a 'zoom-in' on the cancer settled inside the human body can increase the resolution power of key-volatiles detection, allowing the discrimination among different cancer fingerprints. We report this novel technique as a robust support for a better comprehension of the promising results obtained so far and present in literature; it is not to be intended as a replacement for non-invasive breath sampling procedure with the endoscope. (C) 2012 Elsevier Ireland Ltd. All rights reserved.

Santonico, M., Lucantoni, G., Pennazza, G., Capuano, R., G. Galluccio, G., Roscioni, C., et al. (2012). In situ detection Of lung cancer volatile fingerprints using bronchoscopic air-sampling. LUNG CANCER, 77(1), 46-50 [10.1016/j.lungcan.2011.12.010].

In situ detection Of lung cancer volatile fingerprints using bronchoscopic air-sampling

Capuano, R;MARTINELLI, EUGENIO;PAOLESSE, ROBERTO;DI NATALE, CORRADO;
2012-01-01

Abstract

Lung cancer diagnosis via breath analysis has to overcome some issues that can be summarized by two crucial points: (1) further developments for more performant breath sampling technologies; (2) discovering more differentiated volatile fingerprints to be ascribed to specific altered biological mechanisms. The present work merges these two aspects in a pilot study, where a breath volume, sampled via endoscopic probe, is analyzed by an array of non-selective gas sensors. Even if the original non-invasive methods of breath analysis has been laid in favour of the endoscopic means, the innovative technique here proposed allows the analysis of the volatile mixtures directly sampled near the tumor mass. This strategy could open the way for a better understanding of the already obtained discrimination among positive and negative cancer cases. The results obtained so far confirm the established discrimination capacity. This allows to discriminate the different subtypes of lung cancer with 75% of correct classification between adenocarcinoma and squamous cell carcinoma. This result suggests that a 'zoom-in' on the cancer settled inside the human body can increase the resolution power of key-volatiles detection, allowing the discrimination among different cancer fingerprints. We report this novel technique as a robust support for a better comprehension of the promising results obtained so far and present in literature; it is not to be intended as a replacement for non-invasive breath sampling procedure with the endoscope. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
2012
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore CHIM/07 - FONDAMENTI CHIMICI DELLE TECNOLOGIE
Settore ING-INF/01 - ELETTRONICA
English
Con Impact Factor ISI
Exhaled breath, Electronic nose, Lung cancer diagnosis, Bronchoscopy, MS-fingerprint
Santonico, M., Lucantoni, G., Pennazza, G., Capuano, R., G. Galluccio, G., Roscioni, C., et al. (2012). In situ detection Of lung cancer volatile fingerprints using bronchoscopic air-sampling. LUNG CANCER, 77(1), 46-50 [10.1016/j.lungcan.2011.12.010].
Santonico, M; Lucantoni, G; Pennazza, G; Capuano, R; G. Galluccio, G; Roscioni, C; La Delfa, G; Consoli, D; Martinelli, E; Paolesse, R; DI NATALE, C; ...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/69927
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