Circulating Cancer Associated Macrophage-like Cells as a Potential New Prognostic Marker in Pancreatic Ductal Adenocarcinoma.

Circulating Cancer Associated Macrophage-like cells biomarker liquid biopsy pancreatic ductal adenocarcinoma

Journal

Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304

Informations de publication

Date de publication:
17 Nov 2022
Historique:
received: 01 09 2022
revised: 07 11 2022
accepted: 12 11 2022
entrez: 26 11 2022
pubmed: 27 11 2022
medline: 27 11 2022
Statut: epublish

Résumé

Circulating Cancer Associated Macrophage-like cells (CAMLs) have been described as novel liquid biopsy analytes and unfavorable prognostic markers in some tumor entities, with scarce data for Pancreatic Ductal Adenocarcinomas (PDAC). Baseline and follow-up blood was drawn from resected curative ( CAMLs were detectable at baseline in 36.1% of resected patients and 47.4% of palliative PDAC patients. CAML detection was tumor stage independent. Follow-up data indicated that detection of CAMLs (in 45.5% of curative patients) was an independent prognostic factor for shorter recurrence-free survival (RFS) (HR: 4.3, This pilot study shows that detection of CAMLs in PDAC patients can provide prognostic information, either alone or even more pronounced in combination with CTCs, which indicates the power of liquid biopsy marker analyses.

Sections du résumé

BACKGROUND BACKGROUND
Circulating Cancer Associated Macrophage-like cells (CAMLs) have been described as novel liquid biopsy analytes and unfavorable prognostic markers in some tumor entities, with scarce data for Pancreatic Ductal Adenocarcinomas (PDAC).
METHODS METHODS
Baseline and follow-up blood was drawn from resected curative (
RESULTS RESULTS
CAMLs were detectable at baseline in 36.1% of resected patients and 47.4% of palliative PDAC patients. CAML detection was tumor stage independent. Follow-up data indicated that detection of CAMLs (in 45.5% of curative patients) was an independent prognostic factor for shorter recurrence-free survival (RFS) (HR: 4.3,
CONCLUSIONS CONCLUSIONS
This pilot study shows that detection of CAMLs in PDAC patients can provide prognostic information, either alone or even more pronounced in combination with CTCs, which indicates the power of liquid biopsy marker analyses.

Identifiants

pubmed: 36428523
pii: biomedicines10112955
doi: 10.3390/biomedicines10112955
pmc: PMC9687633
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Erich Und Gertrud Roggenbuck Stiftung
ID : 2072-100

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Auteurs

Christine Nitschke (C)

Department of General, Visceral and Thoracic Surgery, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.
Mildred Scheel Cancer Career Center, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.

Benedikt Markmann (B)

Department of General, Visceral and Thoracic Surgery, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.

Leonie Konczalla (L)

Department of General, Visceral and Thoracic Surgery, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.
Mildred Scheel Cancer Career Center, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.

Jolanthe Kropidlowski (J)

Department of Tumor Biology, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.

Thais Pereira-Veiga (T)

Department of Tumor Biology, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.

Pasquale Scognamiglio (P)

Department of General, Visceral and Thoracic Surgery, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.

Martin Schönrock (M)

II Medical Clinic and Polyclinic (Oncology), University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.

Marianne Sinn (M)

II Medical Clinic and Polyclinic (Oncology), University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.

Marie Tölle (M)

Department of General, Visceral and Thoracic Surgery, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.

Jakob Izbicki (J)

Department of General, Visceral and Thoracic Surgery, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.

Klaus Pantel (K)

Department of Tumor Biology, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.

Faik G Uzunoglu (FG)

Department of General, Visceral and Thoracic Surgery, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.

Harriet Wikman (H)

Department of Tumor Biology, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.

Classifications MeSH