Loose Tumor Cells in Pulmonary Arteries of Lung Adenocarcinoma Resection Specimen: No Correlation With Survival, Despite High Prevalence.


Journal

Archives of pathology & laboratory medicine
ISSN: 1543-2165
Titre abrégé: Arch Pathol Lab Med
Pays: United States
ID NLM: 7607091

Informations de publication

Date de publication:
28 Aug 2023
Historique:
accepted: 01 06 2023
medline: 28 8 2023
pubmed: 28 8 2023
entrez: 28 8 2023
Statut: aheadofprint

Résumé

Loose tumor cells and tumor cell clusters can be recognized in the lumen of intratumoral pulmonary arteries of resected non-small cell lung cancer specimens. It is unclear whether these should be considered tumor-emboli, and as such could predict a worsened prognosis. To investigate the nature and prognostic impact of pulmonary artery intraluminal tumor cells. This multicenter study involved an exploratory pilot study and a validation study from 3 institutions. For the exploratory pilot, a retrospective pulmonary resection cohort of primary adenocarcinomas, diagnosed between November 2007 and November 2010, were scored for the presence of tumor cells, as well as potentially other cells in the intravascular spaces using hematoxylin-eosin, and cytokeratin 7 (CK7) stains. In the validation part, 2 retrospective cohorts of resected pulmonary adenocarcinomas, between January 2011 and December 2016, were included. Recurrence-free survival (RFS) and overall survival (OS) data were collected. In the pilot study, CK7+ intravascular cells, mainly tumor cells, were present in 23 of 33 patients (69.7%). The 5-year OS for patients with intravascular tumor cells was 61%, compared with 40% for patients without intravascular tumor cells (P = .19). In the validation study, CK7+ intravascular tumor cells were present in 41 of 70 patients (58.6%). The 5-year RFS for patients with intravascular tumor cells was 80.0%, compared with 80.6% in patients without intravascular tumor cells (P = .52). The 5-year OS rates were, respectively, 82.8% and 71.6% (P = .16). Loose tumor cells in pulmonary arterial lumina were found in most non-small cell lung cancer resection specimens and were not associated with a worse RFS or OS. Therefore, most probably they represent an artifact.

Identifiants

pubmed: 37638545
pii: 495409
doi: 10.5858/arpa.2023-0009-OA
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023 College of American Pathologists.

Déclaration de conflit d'intérêts

The authors have no relevant financial interest in the products or companies described in this article.

Auteurs

Hans Blaauwgeers (H)

From the Department of Pathology, Onze Lieve Vrouwe Gasthuis LAB BV, Amsterdam, the Netherlands (Blaauwgeers).

Federica Filipello (F)

The Department of Pathology, Michele and Pietro Ferrero Hospital, Verduno, Italy (Filipello).

Birgit Lissenberg-Witte (B)

The Department of Epidemiology and Data Science (Lissenberg-Witte), Amsterdam UMC, Location Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.

Claudio Doglioni (C)

The Department of Pathology, San Raffaele Scientific Institute, Milan, Italy (Doglioni).

Teodora Radonic (T)

The Department of Pathology (Radonic, Thunnissen), Amsterdam UMC, Location Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.

Idris Bahce (I)

The Department of Pulmonology (Bahce), Amsterdam UMC, Location Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.

Yuko Minami (Y)

The Department Of Pathology, National Hospital Organization Ibarakihigashi National Hospital, The Center of Chest Diseases and Severe Motor & Intellectual Disabilities, Ibaraki, Japan (Minami).

Andreas Schonau (A)

PathoPulse, Soborg, Denmark (Schonau).

Julien P L Vincenten (JPL)

The Department of Pulmonology, Albert Schweitzer Hospital, Dordrecht, the Netherlands (Vincenten).

Adrianus A J Smit (AAJ)

The Department of Pulmonology, Onze Lieve Vrouwe Gasthuis, Amsterdam, the Netherlands (Smit).

Chris Dickhof (C)

The Department of Surgery and Cardiothoracic Surgery, Amsterdam UMC-Cancer Center Amsterdam, the Netherlands (Dickhof).

Erik Thunnissen (E)

The Department of Pathology (Radonic, Thunnissen), Amsterdam UMC, Location Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.

Classifications MeSH