Importance of carbohydrate antigen (CA 19-9) and carcinoembrionic antigen (CEA) in the prognosis of patients with duodenal adenocarcinoma: a retrospective single-institution cohort study.


Journal

Oncotarget
ISSN: 1949-2553
Titre abrégé: Oncotarget
Pays: United States
ID NLM: 101532965

Informations de publication

Date de publication:
15 04 2023
Historique:
medline: 19 4 2023
entrez: 17 4 2023
pubmed: 18 4 2023
Statut: epublish

Résumé

Duodenal adenocarcinoma (DA) is a rare malignancy without validated tumor markers. In practice, carcinoembryonic antigen (CEA) and carbohydrate antigen (CA 19-9) are often used in the management of DA, though their prognostic value is unknown. A single-institution retrospective review included patients diagnosed with biopsy-confirmed adenocarcinoma of the duodenum between 2006 and 2021. Peri-ampullary tumors were excluded. Levels of CA 19-9 and CEA were collected as continuous variables and were analyzed as binary variables: normal vs. high, using the maximum normal value as a cut-off (normal Ca 19-9 <35 U/ml; CEA <3 ng/ml). Survival analysis was conducted using Kaplan Meier curves, log-rank test and Cox proportional hazards model. There were 68 patients included in the final analysis. Median age was 67 years old and median follow-up time was 22.2 months. CA 19-9 and CEA were elevated in 36.8% and 48.5% of patients, respectively. A concomitant elevation of both tumor markers was associated with worsened OS (HR 2.140, 95% CI: 1.114-4.112; In summary, CA 19-9 and, to a lesser extent, CEA, show promise as prognostic markers in DA. Larger studies are needed to validate their use and to evaluate their performance as markers of recurrence.

Sections du résumé

BACKGROUND
Duodenal adenocarcinoma (DA) is a rare malignancy without validated tumor markers. In practice, carcinoembryonic antigen (CEA) and carbohydrate antigen (CA 19-9) are often used in the management of DA, though their prognostic value is unknown.
MATERIALS AND METHODS
A single-institution retrospective review included patients diagnosed with biopsy-confirmed adenocarcinoma of the duodenum between 2006 and 2021. Peri-ampullary tumors were excluded. Levels of CA 19-9 and CEA were collected as continuous variables and were analyzed as binary variables: normal vs. high, using the maximum normal value as a cut-off (normal Ca 19-9 <35 U/ml; CEA <3 ng/ml). Survival analysis was conducted using Kaplan Meier curves, log-rank test and Cox proportional hazards model.
RESULTS
There were 68 patients included in the final analysis. Median age was 67 years old and median follow-up time was 22.2 months. CA 19-9 and CEA were elevated in 36.8% and 48.5% of patients, respectively. A concomitant elevation of both tumor markers was associated with worsened OS (HR 2.140, 95% CI: 1.114-4.112;
CONCLUSIONS
In summary, CA 19-9 and, to a lesser extent, CEA, show promise as prognostic markers in DA. Larger studies are needed to validate their use and to evaluate their performance as markers of recurrence.

Identifiants

pubmed: 37068159
pii: 28406
doi: 10.18632/oncotarget.28406
pmc: PMC10109526
doi:

Substances chimiques

Carcinoembryonic Antigen 0
Biomarkers, Tumor 0
CA-19-9 Antigen 0
Carbohydrates 0
CA-125 Antigen 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

351-357

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Auteurs

Ellery Altshuler (E)

Department of Internal Medicine, University of Florida, Gainesville, FL 32610, USA.

Raymond Richhart (R)

Department of Internal Medicine, University of Florida, Gainesville, FL 32610, USA.

William King (W)

Department of Internal Medicine, University of Florida, Gainesville, FL 32610, USA.

Mahmoud Aryan (M)

Department of Internal Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

Akash Mathavan (A)

University of Florida College of Medicine, Gainesville, FL 32610, USA.

Akshay Mathavan (A)

University of Florida College of Medicine, Gainesville, FL 32610, USA.

Keegan Hones (K)

University of Florida College of Medicine, Gainesville, FL 32610, USA.

Daniel F Leach (DF)

University of Florida College of Medicine, Gainesville, FL 32610, USA.
Department of Radiation Oncology, University of Florida Health, Gainesville, FL 32601, USA.

Logan Pucci (L)

Department of Internal Medicine, University of Florida, Gainesville, FL 32610, USA.

Joshua Riklan (J)

Department of Internal Medicine, University of Florida, Gainesville, FL 32610, USA.

Pat Haley (P)

Department of Internal Medicine, University of Florida, Gainesville, FL 32610, USA.

Ilyas Sahin (I)

Division of Hematology and Oncology, Department of Medicine, University of Florida, Gainesville, FL 32610, USA.
University of Florida Health Cancer Center, Gainesville, FL 32610, USA.

Brian Ramnaraign (B)

Division of Hematology and Oncology, Department of Medicine, University of Florida, Gainesville, FL 32610, USA.
University of Florida Health Cancer Center, Gainesville, FL 32610, USA.

Sherise Rogers (S)

Division of Hematology and Oncology, Department of Medicine, University of Florida, Gainesville, FL 32610, USA.
University of Florida Health Cancer Center, Gainesville, FL 32610, USA.

Ibrahim Nassour (I)

Division of Surgical Oncology, Department of Surgery, University of Florida, Gainesville, FL 32610, USA.

Steven Hughes (S)

Division of Surgical Oncology, Department of Surgery, University of Florida, Gainesville, FL 32610, USA.

Thomas J George (TJ)

Division of Hematology and Oncology, Department of Medicine, University of Florida, Gainesville, FL 32610, USA.
University of Florida Health Cancer Center, Gainesville, FL 32610, USA.

Jesus Fabregas (J)

Division of Hematology and Oncology, Department of Medicine, University of Florida, Gainesville, FL 32610, USA.
University of Florida Health Cancer Center, Gainesville, FL 32610, USA.

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Classifications MeSH