From CENTRAL to SENTRAL (SErum aNgiogenesis cenTRAL): Circulating Predictive Biomarkers to Anti-VEGFR Therapy.

FGF2 PlGF VEGF angiogenesis bevacizumab circulating biomarkers colon cancer

Journal

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

Informations de publication

Date de publication:
22 May 2020
Historique:
received: 02 04 2020
revised: 16 05 2020
accepted: 18 05 2020
entrez: 28 5 2020
pubmed: 28 5 2020
medline: 28 5 2020
Statut: epublish

Résumé

In the last decade, a series of analyses failed to identify predictive biomarkers of resistance/susceptibility for anti-angiogenic drugs in metastatic colorectal cancer (mCRC). We conducted an exploratory preplanned analysis of serum pro-angiogenic factors (SErum aNgiogenesis-cenTRAL) in 72 mCRC patients enrolled in the phase II CENTRAL (ColorEctalavastiNTRiAlLdh) trial, with the aim to identify potential predictive factors for sensitivity/resistance to first line folinic acid-fluorouracil-irinotecan regimen (FOLFIRI) plus bevacizumab. First-line FOLFIRI/bevacizumab patients were prospectively assessed for the following circulating pro-angiogenic factors, evaluated with ELISA (enzyme-linked immunosorbent assay)-based technique at baseline and at every cycle: Vascular endothelial growth factor A (VEGF-A), hepatocyte growth factor (HGF), stromal derived factor-1 (SDF-1), placental derived growth factor (PlGF), fibroblast growth factor-2 (FGF-2), monocyte chemotactic protein-3 (MCP-3), interleukin-8 (IL-8). Changes in circulating FGF-2 levels among different blood samples seemed to correlate with clinical outcome. Patients who experienced an increase in FGF-2 levels at the second cycle of chemotherapy compared to baseline, had a median Progression Free Survival (mPFS) of 12.85 vs. 7.57 months (Hazard Ratio-HR: 0.73, 95% Confidence Interval-CI: 0.43-1.27, Our pre-planned, prospective analysis suggests that circulating FGF-2 levels' early increase could be used as a marker to identify patients who are more likely to gain benefit from FOLFIRI/bevacizumab first-line therapy.

Sections du résumé

BACKGROUND BACKGROUND
In the last decade, a series of analyses failed to identify predictive biomarkers of resistance/susceptibility for anti-angiogenic drugs in metastatic colorectal cancer (mCRC). We conducted an exploratory preplanned analysis of serum pro-angiogenic factors (SErum aNgiogenesis-cenTRAL) in 72 mCRC patients enrolled in the phase II CENTRAL (ColorEctalavastiNTRiAlLdh) trial, with the aim to identify potential predictive factors for sensitivity/resistance to first line folinic acid-fluorouracil-irinotecan regimen (FOLFIRI) plus bevacizumab.
METHODS METHODS
First-line FOLFIRI/bevacizumab patients were prospectively assessed for the following circulating pro-angiogenic factors, evaluated with ELISA (enzyme-linked immunosorbent assay)-based technique at baseline and at every cycle: Vascular endothelial growth factor A (VEGF-A), hepatocyte growth factor (HGF), stromal derived factor-1 (SDF-1), placental derived growth factor (PlGF), fibroblast growth factor-2 (FGF-2), monocyte chemotactic protein-3 (MCP-3), interleukin-8 (IL-8).
RESULTS RESULTS
Changes in circulating FGF-2 levels among different blood samples seemed to correlate with clinical outcome. Patients who experienced an increase in FGF-2 levels at the second cycle of chemotherapy compared to baseline, had a median Progression Free Survival (mPFS) of 12.85 vs. 7.57 months (Hazard Ratio-HR: 0.73, 95% Confidence Interval-CI: 0.43-1.27,
CONCLUSIONS CONCLUSIONS
Our pre-planned, prospective analysis suggests that circulating FGF-2 levels' early increase could be used as a marker to identify patients who are more likely to gain benefit from FOLFIRI/bevacizumab first-line therapy.

Identifiants

pubmed: 32456056
pii: cancers12051330
doi: 10.3390/cancers12051330
pmc: PMC7281010
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Riccardo Giampieri (R)

Medical Oncology Unit, University Hospital and Università Politecnica delle Marche, 60126 Ancona, Italy.

Pina Ziranu (P)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042 Monserrato, Italy.

Bruno Daniele (B)

Medical Oncology Unit, Ospedale G. Rummo, 82100 Benevento, Italy.

Antonio Zizzi (A)

Medical Oncology Unit, University Hospital and Università Politecnica delle Marche, 60126 Ancona, Italy.

Daris Ferrari (D)

Medical Oncology Unit, Azienda Ospedaliera San Paolo, 20142 Milano, Italy.

Sara Lonardi (S)

Medical Oncology Unit 1, Istituto Oncologico Veneto-IRCCS, 35128 Padova, Italy.

Alberto Zaniboni (A)

Medical Oncology Unit, Fondazione Poliambulanza, 25124 Brescia, Italy.

Luigi Cavanna (L)

Medical Oncology Unit, Ospedale di Piacenza, 29121 Piacenza Italy.

Gerardo Rosati (G)

Medical Oncology Unit, Ospedale San Carlo, 85100 Potenza, Italy.

Mariaelena Casagrande (M)

Medical Oncology Unit, Azienda Ospedaliero Universitaria Santa Maria della Misericordia, 33100 Udine, Italy.

Nicoletta Pella (N)

Medical Oncology Unit, Azienda Ospedaliero Universitaria Santa Maria della Misericordia, 33100 Udine, Italy.

Laura Demurtas (L)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042 Monserrato, Italy.

Maria Giulia Zampino (MG)

Gastrointestinal Medical Oncology Unit and Neuroendocrine Tumors, Istituto Europeo di Oncologia-IRCCS, 20141 Milano, Italy.

Pietro Sozzi (P)

Medical Oncology Unit, Nuovo Ospedale degli Infermi, 13900 Biella, Italy.

Valeria Pusceddu (V)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042 Monserrato, Italy.

Domenico Germano (D)

Medical Oncology Unit, Ospedale G. Rummo, 82100 Benevento, Italy.

Eleonora Lai (E)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042 Monserrato, Italy.

Vittorina Zagonel (V)

Medical Oncology Unit 1, Istituto Oncologico Veneto-IRCCS, 35128 Padova, Italy.

Carla Codecà (C)

Medical Oncology Unit, Azienda Ospedaliera San Paolo, 20142 Milano, Italy.

Michela Libertini (M)

Medical Oncology Unit, Fondazione Poliambulanza, 25124 Brescia, Italy.

Marco Puzzoni (M)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042 Monserrato, Italy.

Roberto Labianca (R)

Medical Oncology Unit, ASST Papa Giovanni XXIII, 24127 Bergamo, Italy.

Stefano Cascinu (S)

IRCCS San Raffaele Scientific Institute Hospital, 20132 Milan, Italy.

Mario Scartozzi (M)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042 Monserrato, Italy.

Classifications MeSH