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A reproducibility study on invasion in small pulmonary adenocarcinoma according to the WHO and a modified classification, supported by biomarkers
E. Thunnissen, H. Blaauwgeers, F. Filipello, B. Lissenberg-Witte, Y. Minami, M. Noguchi, JL. Quesne, MG. Papotti, DB. Flieder, G. Pelosi, I. Sansano, S. Berezowska, A. Ryška, L. Brcic, N. Motoi, Y. Nakatani, C. Kuempers, P. Hofman, V. Hofman, VG....
Language English Country Ireland
Document type Journal Article
- MeSH
- Adenocarcinoma of Lung * pathology metabolism classification diagnosis MeSH
- Adult MeSH
- Neoplasm Invasiveness * MeSH
- Middle Aged MeSH
- Humans MeSH
- Biomarkers, Tumor * metabolism MeSH
- Lung Neoplasms * pathology classification diagnosis MeSH
- Follow-Up Studies MeSH
- Reproducibility of Results MeSH
- Retrospective Studies MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Neoplasm Staging * MeSH
- Case-Control Studies MeSH
- World Health Organization * MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
OBJECTIVES: Evaluating invasion in non-mucinous adenocarcinoma (NMA) of the lung is crucial for accurate pT-staging. This study compares the World Health Organization (WHO) with a recently modified NMA classification. MATERIALS AND METHODS: A retrospective case-control study was conducted on small NMA pT1N0M0 cases with a 5-year follow-up. Seventy cases were reviewed by 42 pulmonary pathologists first according to the WHO classification and after tutorial according to a modified classification. A third round was conducted based on feedback from 41 peers of previous rounds. Additionally, orthogonal biomarker analysis was performed. RESULTS: In the first two rounds, 42 pathologists from 13 countries assessed all 70 cases, while 36 pathologists evaluated 41 non-unanimous cases in the third round. Kappa values for invasiveness increased in rounds 1, 2, and 3 to 0.27, 0.45 and 0.62, respectively. In contrast to low variation in total tumor size measurements (6 %), a marked increase in invasive tumor size variation was observed (42 %), which was associated with high uncertainty. In the third round 10 cases were non-invasive, all without recurrence. The modified classification showed in the 3rd round marked reduction of the variation in pT staging compared to the current WHO classification. Proliferation rate, tumor mutational burden, and transcriptomic profiles supported the distinction between invasive cases and non-invasive cases of the modified classification. CONCLUSION: The modified classification demonstrates essentially higher reproducibility compared to the current WHO classification in NMA. The modified classification proves valuable in identifying low-risk lesions that are entirely non-invasive, and is supported by biomarker analysis.
Center for Personalized Medicine Heidelberg Heidelberg Germany
Dept of Epidemiology and Data Science Amsterdam UMC VU University Amsterdam the Netherlands
Dept of Pathology Aarhus University Aarhus Denmark
Dept of Pathology Amsterdam UMC VU University Amsterdam the Netherlands
Dept of Pathology Canisius Wilhelmina Hospital Nijmegen the Netherlands
Dept of Pathology Charles University ESP Hradec Kralove Czech Republic
Dept of Pathology CRUK Beatson Cancer Research Institute Glasgow Scotland UK
Dept of Pathology Department of Oncology and Hemato Oncology University of Milan Milan Italy
Dept of Pathology Erasmus Medical Center Rotterdam the Netherlands
Dept of Pathology Fondazione Poliambulanza Hospital Institute Brescia Brescia Italy
Dept of Pathology Fox Chase Cancer Center Philadelphia PA USA
Dept of Pathology Hospital Universitari Vall d'Hebron Barcelona Spain
Dept of Pathology HUS Helsinki University Hospital Helsinki Finland
Dept of Pathology International University of Health and Welfare Mita Hospital Tokyo Japan
Dept of Pathology Jichi Medical University Tochigi Japan
Dept of Pathology LabPON Hengelo the Netherlands
Dept of Pathology Lausanne University Hospital and University of Lausanne Lausanne Switzerland
Dept of Pathology Maggiore Hospital University of Bologna Bologna Italy
Dept of Pathology Meander Medisch Centrum Amersfoort the Netherlands
Dept of Pathology Medical University of Graz Graz Austria
Dept of Pathology Mount Sinai Medical Center New York NY USA
Dept of Pathology Naritatomisato Tokushukai Hospital Chiba Japan
Dept of Pathology National Hospital Organization Ibarakihigashi National Hospital Tokai Japan
Dept of Pathology National Institute of Pneumology M Nasta Bucharest Romania
Dept of Pathology OLVG LAB BV Amsterdam the Netherlands
Dept of Pathology Padova University Hospital Padova Italy
Dept of Pathology Rijnstate Ziekenhuis Arnhem the Netherlands
Dept of Pathology Saitama Cancer Center Saitama Japan
Dept of Pathology San Raffaele Scientific Institute Milan Italy
Dept of Pathology School of Cancer Sciences University of Glasgow Scotland UK
Dept of Pathology St James's Hospital Dublin Ireland
Dept of Pathology St Olavs Hospital Trondheim University Hospital Trondheim Norway
Dept of Pathology Universitätsklinikum Schleswig Holstein Campus Lübeck Lübeck Germany
Dept of Pathology University Clinic Golnik Golnik Slovenia
Dept of Pathology University College London Cancer Institute London United Kingdom
Dept of Pathology University Medical Center Groningen Groningen the Netherlands
Dept of Pathology University of California San Francisco CA USA
Dept of Pathology University of Turin Turin Italy
Dept of Pathology UZ Leuven Leuven Belgium
Dept of Pathology Yale School of Medicine New Haven CT USA
Dept of Pathology Yokosuka Kyosai Hospital Yokosuka Japan
Dept Pathologie DNA St Antoniusziekenhuis Nieuwegein the Netherlands
Institute of Pathology Heidelberg University Hospital Heidelberg Germany
Norwegian University of Science and Technology Trondheim Norway
References provided by Crossref.org
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- $a Thunnissen, Erik $u Dept. of Pathology, Amsterdam UMC, VU University, Amsterdam, the Netherlands. Electronic address: e.thunnissen@amsterdamumc.nl
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- $a A reproducibility study on invasion in small pulmonary adenocarcinoma according to the WHO and a modified classification, supported by biomarkers / $c E. Thunnissen, H. Blaauwgeers, F. Filipello, B. Lissenberg-Witte, Y. Minami, M. Noguchi, JL. Quesne, MG. Papotti, DB. Flieder, G. Pelosi, I. Sansano, S. Berezowska, A. Ryška, L. Brcic, N. Motoi, Y. Nakatani, C. Kuempers, P. Hofman, V. Hofman, VG. Dale, G. Rossi, F. Ambrosi, D. Matsubara, Y. Ishikawa, B. Weynand, F. Calabrese, F. Pezzuto, I. Kern, S. Nicholson, A. Mutka, S. Dacic, MB. Beasley, G. Arrigoni, W. Timens, M. Ooft, M. Brinkhuis, N. Bulkmans, R. Britstra, W. Vreuls, KD. Jones, JH. von der Thüsen, H. Hager, S. Perner, D. Moore, DG. Leonte, S. Al-Janabi, A. Schønau, O. Neumann, K. Kluck, I. Ourailidis, M. Ball, J. Budczies, D. Kazdal, A. Stenzinger
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- $a OBJECTIVES: Evaluating invasion in non-mucinous adenocarcinoma (NMA) of the lung is crucial for accurate pT-staging. This study compares the World Health Organization (WHO) with a recently modified NMA classification. MATERIALS AND METHODS: A retrospective case-control study was conducted on small NMA pT1N0M0 cases with a 5-year follow-up. Seventy cases were reviewed by 42 pulmonary pathologists first according to the WHO classification and after tutorial according to a modified classification. A third round was conducted based on feedback from 41 peers of previous rounds. Additionally, orthogonal biomarker analysis was performed. RESULTS: In the first two rounds, 42 pathologists from 13 countries assessed all 70 cases, while 36 pathologists evaluated 41 non-unanimous cases in the third round. Kappa values for invasiveness increased in rounds 1, 2, and 3 to 0.27, 0.45 and 0.62, respectively. In contrast to low variation in total tumor size measurements (6 %), a marked increase in invasive tumor size variation was observed (42 %), which was associated with high uncertainty. In the third round 10 cases were non-invasive, all without recurrence. The modified classification showed in the 3rd round marked reduction of the variation in pT staging compared to the current WHO classification. Proliferation rate, tumor mutational burden, and transcriptomic profiles supported the distinction between invasive cases and non-invasive cases of the modified classification. CONCLUSION: The modified classification demonstrates essentially higher reproducibility compared to the current WHO classification in NMA. The modified classification proves valuable in identifying low-risk lesions that are entirely non-invasive, and is supported by biomarker analysis.
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