Baseline Cytokine Profile Identifies a Favorable Outcome in a Subgroup of Colorectal Cancer Patients Treated with Regorafenib.

PCA cytokine profile cytokinome mCRC regorafenib

Journal

Vaccines
ISSN: 2076-393X
Titre abrégé: Vaccines (Basel)
Pays: Switzerland
ID NLM: 101629355

Informations de publication

Date de publication:
02 Feb 2023
Historique:
received: 22 12 2022
revised: 28 01 2023
accepted: 31 01 2023
entrez: 28 2 2023
pubmed: 1 3 2023
medline: 1 3 2023
Statut: epublish

Résumé

Metastatic colorectal cancer is frequently associated with poor clinical conditions that may limit therapeutic options. Regorafenib is a small molecule approved for the treatment of metastatic colorectal cancer, but it is hampered by significative toxicities. Moreover, only a relatively limited number of patients benefit from the treatment. Therefore, the identification of reliable markers for response is an unmet need. Eighteen cytokines, selected based on their prevalent Th1 or Th2 effects, were collected. Peripheral blood samples were gathered at baseline in 25 metastatic colorectal cancer patients treated with regorafenib. Data extracted have been linked to progression-free survival. ROC identified the best cytokines associated with outcome. The relative value of the selected cytokines was determined by PCA. Data analysis identified 8 cytokines (TGF-β, TNF-α, CCL-2, IL-6, IL-8, IL-10, IL-13 and IL-21), used to create a signature (TGF-β, TNF-α high; CCL-2, IL-6, IL-8, IL-10, IL-13 and IL-21 low) corresponding to patients with a significantly longer progression-free survival. This report suggests that the analysis of multiple cytokines might identify a cytokine signature related to a patient's outcome that is able to recognize patients who will benefit from treatment. If confirmed, future studies, also based on different drugs, using this approach and including larger patient populations, might identify a signature allowing the a priori identification of patients to be treated.

Identifiants

pubmed: 36851213
pii: vaccines11020335
doi: 10.3390/vaccines11020335
pmc: PMC9959285
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Andrea Abbona (A)

Fondazione Arco Cuneo, 12100 Cuneo, Italy.

Vincenzo Ricci (V)

Medical Oncology Unit, AORN "San Pio", 82100 Benevento, Italy.

Matteo Paccagnella (M)

Fondazione Arco Cuneo, 12100 Cuneo, Italy.

Cristina Granetto (C)

Azienda Ospedaliera S. Croce e Carle, 12100 Cuneo, Italy.

Fiorella Ruatta (F)

Department of Medical Oncology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milano, Italy.

Carolina Cauchi (C)

Department of Medical Oncology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milano, Italy.

Danilo Galizia (D)

Candiolo Cancer Institute, FPO-IRCCS, 10060 Candiolo, Italy.

Michele Ghidini (M)

Department of Medical Oncology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milano, Italy.

Nerina Denaro (N)

Department of Medical Oncology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milano, Italy.

Marco Carlo Merlano (MC)

Candiolo Cancer Institute, FPO-IRCCS, 10060 Candiolo, Italy.

Ornella Garrone (O)

Department of Medical Oncology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milano, Italy.

Classifications MeSH