Computer-based intensity measurement assists pathologists in scoring phosphatase and tensin homolog immunohistochemistry: clinical associations in NSCLC patients of the European thoracic oncology platform lungscape cohort
Introduction - Phosphatase and tensin homolog (PTEN) loss is frequently observed in NSCLC and associated with both phosphoinositide 3-kinase activation and tumoral immunosuppression. PTEN immunohistochemistry is a valuable readout, but lacks standardized staining protocol and cutoff value. - Methods...
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| Hauptverfasser: | , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
18 September 2018
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| In: |
Journal of thoracic oncology
Year: 2018, Jahrgang: 13, Heft: 12, Pages: 1851-1863 |
| ISSN: | 1556-1380 |
| DOI: | 10.1016/j.jtho.2018.08.2034 |
| Online-Zugang: | Verlag, Volltext: https://doi.org/10.1016/j.jtho.2018.08.2034 Verlag, Volltext: http://www.sciencedirect.com/science/article/pii/S1556086418330533 
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| Verfasserangaben: | Undine Rulle, MSc, Zoi Tsourti, PhD, Ruben Casanova, PhD, Karl-Friedrich Deml, MD, Eric Verbeken, MD, PhD, Erik Thunnissen, MD, PhD, Arne Warth, MD, Richard Cheney, MD, Aleksandra Sejda, MD, Ernst Jan Speel, MD, PhD, Line Bille Madsen, MD, Daisuke Nonaka, MD, Atilio Navarro, MD, Irene Sansano, MD, Antonio Marchetti, MD, PhD, Stephen P. Finn, MD, PhD, Kim Monkhorst, MD, PhD, Keith M. Kerr, MB, Martina Haberecker, MD, Chengguang Wu, MSc, Panagiota Zygoura, MSc, Roswitha Kammler, BA, Thomas Geiger, PhD, Steven Gendreau, PhD, Katja Schulze, PhD, Bart Vrugt, MD, PhD, Peter Wild, MD, PhD, Holger Moch, MD, PhD, Walter Weder, MD, AtaTunaCiftlik,PhD, Urania Dafni, ScD, Solange Peters, MD, PhD, Lukas Bubendorf, MD, PhD, Rolf A. Stahel, MD, Alex Soltermann, MD, PhD |
MARC
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| 520 | |a Introduction - Phosphatase and tensin homolog (PTEN) loss is frequently observed in NSCLC and associated with both phosphoinositide 3-kinase activation and tumoral immunosuppression. PTEN immunohistochemistry is a valuable readout, but lacks standardized staining protocol and cutoff value. - Methods - After an external quality assessment using SP218, 138G6 and 6H2.1 anti-PTEN antibodies, scored on webbook and tissue microarray, the European Thoracic Oncology Platform cohort samples (n = 2245 NSCLC patients, 8980 tissue microarray cores) were stained with SP218. All cores were H-scored by pathologists and by computerized pixel-based intensity measurements calibrated by pathologists. - Results - All three antibodies differentiated six PTEN+ versus six PTEN- cases on external quality assessment. For 138G6 and SP218, high sensitivity and specificity was found for all H-score threshold values including prospectively defined 0, calculated 8 (pathologists), and calculated 5 (computer). High concordance among pathologists in setting computer-based intensities and between pathologists and computer in H-scoring was observed. Because of over-integration of the human eye, pixel-based computer H-scores were overall 54% lower. For all cutoff values, PTEN- was associated with smoking history, squamous cell histology, and higher tumor stage (p < 0.001). In adenocarcinomas, PTEN- was associated with poor survival. - Conclusion - Calibration of immunoreactivity intensities by pathologists following computerized H-score measurements has the potential to improve reproducibility and homogeneity of biomarker detection regarding epitope validation in multicenter studies. | ||
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| 650 | 4 | |a External quality assessment | |
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