Cachexia-Affected Survival Based on Inflammatory Parameters Compared to Complex Conventional Nutritional Assessments in Patients with Pancreatic Cancer and Other Gastrointestinal Tumors-The CONKO 020 Investigation.

CRP IL-6 PDAC cachexia survival systemic inflammation

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
18 Mar 2024
Historique:
received: 11 02 2024
revised: 11 03 2024
accepted: 11 03 2024
medline: 28 3 2024
pubmed: 28 3 2024
entrez: 28 3 2024
Statut: epublish

Résumé

Pancreatic adenocarcinoma (PDAC) is still a complex, devastating disease. Cachexia symptoms frequently impair patient survival. This accompanying syndrome is commonly diagnosed late, when clinical signs become evident. Early diagnosis using conventional measurement methods is often difficult, and the discrimination of this disease from cancer progression is challenging and often overlaps. The aim of this study was to analyze whether conventional nutritional assessments or laboratory biomarkers are better predictive tools for the early detection of patients at risk of reduced survival. We analyzed a prospective predefined cohort of 182 patients with gastrointestinal cancer, 120 patients with PDAC and-as controls-62 patients with other gastrointestinal adenocarcinoma (oAC), from whom we have sufficient data of protocol-defined conventional nutritional assessments, clinical data, and specific laboratory parameters. at the time of tumor diagnosis, high inflammatory biomarkers (c-reactive protein (CRP), interleukin-6 (IL-6)) and albumin serum levels were associated with impaired OS in PDAC patients, but not in patients with oAC. Hemoglobin, body mass index (BMI), and bioelectrical assessments alone did not have a prognostic impact at the time of diagnosis. In a multivariate analysis, only CRP (HR 1.91 (1.25-2.92), Specifically for PDAC patients, high inflammatory index and albumin serum levels potentially represent a sufficient early surrogate marker to detect patients at high risk of impaired OS better than complex conventional methods. These findings could help to identify patients who may benefit from early therapeutic interventions.

Sections du résumé

BACKGROUND BACKGROUND
Pancreatic adenocarcinoma (PDAC) is still a complex, devastating disease. Cachexia symptoms frequently impair patient survival. This accompanying syndrome is commonly diagnosed late, when clinical signs become evident. Early diagnosis using conventional measurement methods is often difficult, and the discrimination of this disease from cancer progression is challenging and often overlaps. The aim of this study was to analyze whether conventional nutritional assessments or laboratory biomarkers are better predictive tools for the early detection of patients at risk of reduced survival.
METHODS METHODS
We analyzed a prospective predefined cohort of 182 patients with gastrointestinal cancer, 120 patients with PDAC and-as controls-62 patients with other gastrointestinal adenocarcinoma (oAC), from whom we have sufficient data of protocol-defined conventional nutritional assessments, clinical data, and specific laboratory parameters.
RESULTS RESULTS
at the time of tumor diagnosis, high inflammatory biomarkers (c-reactive protein (CRP), interleukin-6 (IL-6)) and albumin serum levels were associated with impaired OS in PDAC patients, but not in patients with oAC. Hemoglobin, body mass index (BMI), and bioelectrical assessments alone did not have a prognostic impact at the time of diagnosis. In a multivariate analysis, only CRP (HR 1.91 (1.25-2.92),
CONCLUSION CONCLUSIONS
Specifically for PDAC patients, high inflammatory index and albumin serum levels potentially represent a sufficient early surrogate marker to detect patients at high risk of impaired OS better than complex conventional methods. These findings could help to identify patients who may benefit from early therapeutic interventions.

Identifiants

pubmed: 38539528
pii: cancers16061194
doi: 10.3390/cancers16061194
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Charité - Universitätsmedizin Berlin
ID : 51432176

Auteurs

Johanna W Meyer-Knees (JW)

Division of Oncology and Hematology, Berlin Institute of Health, Charite Campus Virchow Klinikum, Freie Universität Berlin, Humboldt Universität zu Berlin, 13353 Berlin, Germany.

Janina Falkenthal (J)

KONZ-E-B-T CARE GmbH Zentrum für Ernährung, Beatmung und Therapie, 13435 Berlin, Germany.

Dominik Geisel (D)

Division of Radiology, Berlin Institute of Health, Charite Campus Virchow Klinikum, Freie Universität Berlin, Humboldt Universität zu Berlin, 13353 Berlin, Germany.

Christopher C M Neumann (CCM)

Division of Oncology and Hematology, Berlin Institute of Health, Charite Campus Mitte, Freie Universität Berlin, Humboldt Universität zu Berlin, 10117 Berlin, Germany.

Georg Hilfenhaus (G)

Division of Oncology and Hematology, Berlin Institute of Health, Charite Campus Mitte, Freie Universität Berlin, Humboldt Universität zu Berlin, 10117 Berlin, Germany.

Lars U Stephan (LU)

Division of Oncology and Hematology, Berlin Institute of Health, Charite Campus Mitte, Freie Universität Berlin, Humboldt Universität zu Berlin, 10117 Berlin, Germany.

Wenzel Schöning (W)

Division of Surgery, Berlin Institute of Health, Charite Campus Mitte-Campus Virchow Klinikum, Freie Universität Berlin, Humboldt Universität zu Berlin, 13353 Berlin, Germany.

Thomas Malinka (T)

Division of Surgery, Berlin Institute of Health, Charite Campus Mitte-Campus Virchow Klinikum, Freie Universität Berlin, Humboldt Universität zu Berlin, 13353 Berlin, Germany.

Johann Pratschke (J)

Division of Surgery, Berlin Institute of Health, Charite Campus Mitte-Campus Virchow Klinikum, Freie Universität Berlin, Humboldt Universität zu Berlin, 13353 Berlin, Germany.

Sebastian Stintzing (S)

Division of Oncology and Hematology, Berlin Institute of Health, Charite Campus Mitte, Freie Universität Berlin, Humboldt Universität zu Berlin, 10117 Berlin, Germany.

Uwe Pelzer (U)

Division of Oncology and Hematology, Berlin Institute of Health, Charite Campus Mitte, Freie Universität Berlin, Humboldt Universität zu Berlin, 10117 Berlin, Germany.

Classifications MeSH