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Circulating tumor cells as a preoperative risk marker for occult metastases in patients with resectable cholangiocarcinoma

Cholangiocarcinoma (CCA) is an aggressive tumor associated with a high rate of recurrence after resection. An important risk factor for recurrence is the presence of occult metasta-ses, which are not radiologically detectable at the time of diagnosis. There are currently no biomarkers for the preope...

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Autores principales: Fründt, Thorben, von Felden, Johann, Krause, Jenny, Heumann, Asmus, Li, Jun, Riethdorf, Sabine, Pantel, Klaus, Huber, Samuel, Lohse, Ansgar W., Wege, Henning, Schulze, Kornelius
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9685781/
https://www.ncbi.nlm.nih.gov/pubmed/36439492
http://dx.doi.org/10.3389/fonc.2022.941660
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author Fründt, Thorben
von Felden, Johann
Krause, Jenny
Heumann, Asmus
Li, Jun
Riethdorf, Sabine
Pantel, Klaus
Huber, Samuel
Lohse, Ansgar W.
Wege, Henning
Schulze, Kornelius
author_facet Fründt, Thorben
von Felden, Johann
Krause, Jenny
Heumann, Asmus
Li, Jun
Riethdorf, Sabine
Pantel, Klaus
Huber, Samuel
Lohse, Ansgar W.
Wege, Henning
Schulze, Kornelius
author_sort Fründt, Thorben
collection PubMed
description Cholangiocarcinoma (CCA) is an aggressive tumor associated with a high rate of recurrence after resection. An important risk factor for recurrence is the presence of occult metasta-ses, which are not radiologically detectable at the time of diagnosis. There are currently no biomarkers for the preoperative assessment of micrometastases. A previous study demonstrated the prognostic relevance of circulating tumor cells (CTC) in patients with advanced CCA but the potential of CTCs as a preoperative marker for detecting occult metastases has not been investigated so far. In this two-phase study, we first recruited a cohort of 27 patients with histologically proven, metastatic CCA or gallbladder cancer (GBCA) to assess feasibility (feasibility cohort, FC). CTCs were measured in the peripheral blood using the CellSearch System (CSS) between October 2012 and January 2017. Subsequently, in 11 patients undergoing curative-intended resection for CCA (intrahepatic CCA: n =4; extrahepatic CCA n= 6; gallbladder cancer: n=1), peripheral and central venous blood specimens were obtained to improve detection rate by simultaneous measurement and to elucidate distribution of CTCs in different venous compartments. Presence of CTCs detection was correlated with postoperative TNM-status. In the FC, CTCs (range 1-3 cells, median: 1) were detected in 40% (11/27) patients and were signifi-cantly associated with worse overall survival (hazard ratio: 3.59; 95% CI: 1.79- 7.1; p = 0.04). By combined peripheral and central measurement, CTC detection was increased to 54% (6/11) in the resection cohort (RC) and was associated with metastases that were only identified during the surgical procedure (peritoneal carcinoma: n = 1; infiltration of the duodenum: n = 1) or immediately after surgery (evidence of pulmonary metastases by CT scan two days after resection, not evident on initial tumor staging prior resection). Taken together, in this single center pilot study, we demonstrated that CTCs are detectable in CCA patients and are associated with significantly impaired survival in patients at metastatic stage. Detection rate prior to surgery was improved to >50% by combined peripheral and central measurement. Moreover, preoperative CTC detection may indicate existing metastases and could help to stratify patients more accurately.
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spelling pubmed-96857812022-11-25 Circulating tumor cells as a preoperative risk marker for occult metastases in patients with resectable cholangiocarcinoma Fründt, Thorben von Felden, Johann Krause, Jenny Heumann, Asmus Li, Jun Riethdorf, Sabine Pantel, Klaus Huber, Samuel Lohse, Ansgar W. Wege, Henning Schulze, Kornelius Front Oncol Oncology Cholangiocarcinoma (CCA) is an aggressive tumor associated with a high rate of recurrence after resection. An important risk factor for recurrence is the presence of occult metasta-ses, which are not radiologically detectable at the time of diagnosis. There are currently no biomarkers for the preoperative assessment of micrometastases. A previous study demonstrated the prognostic relevance of circulating tumor cells (CTC) in patients with advanced CCA but the potential of CTCs as a preoperative marker for detecting occult metastases has not been investigated so far. In this two-phase study, we first recruited a cohort of 27 patients with histologically proven, metastatic CCA or gallbladder cancer (GBCA) to assess feasibility (feasibility cohort, FC). CTCs were measured in the peripheral blood using the CellSearch System (CSS) between October 2012 and January 2017. Subsequently, in 11 patients undergoing curative-intended resection for CCA (intrahepatic CCA: n =4; extrahepatic CCA n= 6; gallbladder cancer: n=1), peripheral and central venous blood specimens were obtained to improve detection rate by simultaneous measurement and to elucidate distribution of CTCs in different venous compartments. Presence of CTCs detection was correlated with postoperative TNM-status. In the FC, CTCs (range 1-3 cells, median: 1) were detected in 40% (11/27) patients and were signifi-cantly associated with worse overall survival (hazard ratio: 3.59; 95% CI: 1.79- 7.1; p = 0.04). By combined peripheral and central measurement, CTC detection was increased to 54% (6/11) in the resection cohort (RC) and was associated with metastases that were only identified during the surgical procedure (peritoneal carcinoma: n = 1; infiltration of the duodenum: n = 1) or immediately after surgery (evidence of pulmonary metastases by CT scan two days after resection, not evident on initial tumor staging prior resection). Taken together, in this single center pilot study, we demonstrated that CTCs are detectable in CCA patients and are associated with significantly impaired survival in patients at metastatic stage. Detection rate prior to surgery was improved to >50% by combined peripheral and central measurement. Moreover, preoperative CTC detection may indicate existing metastases and could help to stratify patients more accurately. Frontiers Media S.A. 2022-11-10 /pmc/articles/PMC9685781/ /pubmed/36439492 http://dx.doi.org/10.3389/fonc.2022.941660 Text en Copyright © 2022 Fründt, von Felden, Krause, Heumann, Li, Riethdorf, Pantel, Huber, Lohse, Wege and Schulze https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Fründt, Thorben
von Felden, Johann
Krause, Jenny
Heumann, Asmus
Li, Jun
Riethdorf, Sabine
Pantel, Klaus
Huber, Samuel
Lohse, Ansgar W.
Wege, Henning
Schulze, Kornelius
Circulating tumor cells as a preoperative risk marker for occult metastases in patients with resectable cholangiocarcinoma
title Circulating tumor cells as a preoperative risk marker for occult metastases in patients with resectable cholangiocarcinoma
title_full Circulating tumor cells as a preoperative risk marker for occult metastases in patients with resectable cholangiocarcinoma
title_fullStr Circulating tumor cells as a preoperative risk marker for occult metastases in patients with resectable cholangiocarcinoma
title_full_unstemmed Circulating tumor cells as a preoperative risk marker for occult metastases in patients with resectable cholangiocarcinoma
title_short Circulating tumor cells as a preoperative risk marker for occult metastases in patients with resectable cholangiocarcinoma
title_sort circulating tumor cells as a preoperative risk marker for occult metastases in patients with resectable cholangiocarcinoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9685781/
https://www.ncbi.nlm.nih.gov/pubmed/36439492
http://dx.doi.org/10.3389/fonc.2022.941660
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