TY - JOUR
T1 - Loose Tumor Cells in Pulmonary Arteries of Lung Adenocarcinoma Resection Specimen
T2 - No Correlation With Survival, Despite High Prevalence
AU - Blaauwgeers, Hans
AU - Filipello, Federica
AU - Lissenberg-Witte, Birgit
AU - Doglioni, Claudio
AU - Radonic, Teodora
AU - Bahce, Idris
AU - Minami, Yuko
AU - Schonau, Andreas
AU - Vincenten, Julien P L
AU - Smit, Adrianus A J
AU - Dickhof, Chris
AU - Thunnissen, Erik
N1 - © 2023 College of American Pathologists.
PY - 2023/8/28
Y1 - 2023/8/28
N2 - CONTEXT.—: 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.OBJECTIVE.—: To investigate the nature and prognostic impact of pulmonary artery intraluminal tumor cells.DESIGN.—: 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.RESULTS.—: 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).CONCLUSIONS.—: 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.
AB - CONTEXT.—: 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.OBJECTIVE.—: To investigate the nature and prognostic impact of pulmonary artery intraluminal tumor cells.DESIGN.—: 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.RESULTS.—: 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).CONCLUSIONS.—: 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.
U2 - https://doi.org/10.5858/arpa.2023-0009-OA
DO - https://doi.org/10.5858/arpa.2023-0009-OA
M3 - Article
C2 - 37638545
SN - 0003-9985
JO - Archives of Pathology & Laboratory Medicine
JF - Archives of Pathology & Laboratory Medicine
ER -