Prognostic Significance of IGF-1 Signalling Pathway in Patients With Advanced Non-small Cell Lung Cancer.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 14 06 2019
revised: 27 06 2019
accepted: 28 06 2019
entrez: 2 8 2019
pubmed: 2 8 2019
medline: 8 8 2019
Statut: ppublish

Résumé

Insulin-like growth factor 1 (IGF-1)-mediated molecular pathway has been implicated in non-small cell lung cancer (NSCLC) pathogenesis and progression. We aimed to evaluate serum levels of IGF-1, IGF-2 and IGF-binding protein 3 (IGF-BP3) before and after standard treatment in patients with advanced NSCLC and their prognostic and predictive correlations. Seventy-three patients were prospectively included. Analysis and quantification of circulating levels of IGF1, IGF2, IGFBP3 were performed by total ELISA in peripheral blood samples at baseline and 3 months post-treatment. The median values of IGF-1 and IGF-1/IGF-BP3 ratios (125.82 vs. 133.4 ng/ml, p=0.087 and 0.01006 vs. 0.01252, p=0.011) were both decreased after treatment. Importantly, the post-treatment value of the ratio was significantly reduced only among responders to treatment (0.01044 from 0.01255, p=0.02). Reduction of IGF-1/IGF-BP3 ratio was statistically significant only among patients with NSCLC who responded to first-line treatment. If validated in larger cohorts, IGF-1/IGFBP3 might be a useful predictive tool for response to chemotherapy in NSCLC.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
Insulin-like growth factor 1 (IGF-1)-mediated molecular pathway has been implicated in non-small cell lung cancer (NSCLC) pathogenesis and progression. We aimed to evaluate serum levels of IGF-1, IGF-2 and IGF-binding protein 3 (IGF-BP3) before and after standard treatment in patients with advanced NSCLC and their prognostic and predictive correlations.
PATIENTS AND METHODS METHODS
Seventy-three patients were prospectively included. Analysis and quantification of circulating levels of IGF1, IGF2, IGFBP3 were performed by total ELISA in peripheral blood samples at baseline and 3 months post-treatment.
RESULTS RESULTS
The median values of IGF-1 and IGF-1/IGF-BP3 ratios (125.82 vs. 133.4 ng/ml, p=0.087 and 0.01006 vs. 0.01252, p=0.011) were both decreased after treatment. Importantly, the post-treatment value of the ratio was significantly reduced only among responders to treatment (0.01044 from 0.01255, p=0.02).
CONCLUSION CONCLUSIONS
Reduction of IGF-1/IGF-BP3 ratio was statistically significant only among patients with NSCLC who responded to first-line treatment. If validated in larger cohorts, IGF-1/IGFBP3 might be a useful predictive tool for response to chemotherapy in NSCLC.

Identifiants

pubmed: 31366504
pii: 39/8/4185
doi: 10.21873/anticanres.13578
doi:

Substances chimiques

Biomarkers, Tumor 0
IGF2 protein, human 0
Insulin-Like Growth Factor Binding Protein 3 0
Recombinant Proteins 0
Pemetrexed 04Q9AIZ7NO
Insulin-Like Growth Factor I 67763-96-6
Insulin-Like Growth Factor II 67763-97-7
mecasermin 7GR9I2683O

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4185-4190

Informations de copyright

Copyright© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Ioannis Kotsantis (I)

Section of Medical Oncology, Department of Internal Medicine, Faculty of Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Athens, Greece.

Panagiota Economopoulou (P)

Section of Medical Oncology, Department of Internal Medicine, Faculty of Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Athens, Greece.

Amanda Psyrri (A)

Section of Medical Oncology, Department of Internal Medicine, Faculty of Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Athens, Greece psyrri237@yahoo.com.

Eirini Maratou (E)

Hellenic National Center for the Research, Prevention and Treatment of Diabetes Mellitus and its Complications (H.N.D.C), Athens, Greece.

Dimitrios Pectasides (D)

Oncology Section, Second Department of Internal Medicine, Hippokration Hospital, Athens, Greece.

Helen Gogas (H)

First Department of Internal Medicine, Laiko General Hospital, National and Kapodistrian University of Athens School of Medicine, Athens, Greece.

Nikolaos Kentepozidis (N)

Department of Medical Oncology, 251 Airforce General Hospital, Athens, Greece.

Giannis Mountzios (G)

Department of Medical Oncology, 251 Airforce General Hospital, Athens, Greece.

George Dimitriadis (G)

Second Department of Internal Medicine and Research Institute, Faculty of Medicine, National and Kapodistrian University of Athens, University General Hospital Attikon, Athens, Greece.

Stavroula Giannouli (S)

Second Department of Internal Medicine, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

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Classifications MeSH