Serum IGF-1 Scores and Clinical Outcomes in the Phase III IMbrave150 Study of Atezolizumab Plus Bevacizumab versus Sorafenib in Patients with Unresectable Hepatocellular Carcinoma.
HCC
IGF-CTP score
immunotherapy
prognostic biomarker
Journal
Journal of hepatocellular carcinoma
ISSN: 2253-5969
Titre abrégé: J Hepatocell Carcinoma
Pays: New Zealand
ID NLM: 101674775
Informations de publication
Date de publication:
2022
2022
Historique:
received:
22
04
2022
accepted:
16
07
2022
entrez:
18
10
2022
pubmed:
19
10
2022
medline:
19
10
2022
Statut:
epublish
Résumé
Child-Turcotte-Pugh class A (CTP-A) in unresectable hepatocellular carcinoma (HCC) is the standard criterion for active therapy and clinical trial enrollment. We hypothesized that insulin-like growth factor-1 (IGF-1) derived scores may provide improved survival prediction over CTP classification. This study aimed to evaluate the potential prognostic and predictive effects of IGF-1 derived scores in the phase III IMbrave150 study. Baseline and on-treatment serum IGF-1 levels from 371 patients were subjected to central analysis. Patients' IGF-1 score (1/2/3) and IGF-CTP score (A/B/C) were determined based on pre-specified cutoffs. Outcomes were analyzed by baseline and by on-treatment changes of the IGF-1 and IGF-CTP scores within and between the two treatment arms. The interaction between these scores and outcomes was assessed using univariate and multivariate analyses. Baseline IGF-CTP score (A vs B/C) showed prognostic significance for OS in both the atezolizumab-bevacizumab (hazard ratio [HR], 0.33; 95% confidence interval [CI], 0.20-0.56; Baseline and kinetic change of IGF-CTP and IGF-1 scores are independent prognostic factors for patients with unresectable HCC treated with atezolizumab-bevacizumab or sorafenib. These novel scores may provide improved patient stratification in future HCC clinical trials. IMbrave150 ClincialTrials.gov number, NCT03434379.
Identifiants
pubmed: 36254201
doi: 10.2147/JHC.S369951
pii: 369951
pmc: PMC9569161
doi:
Banques de données
ClinicalTrials.gov
['NCT03434379']
Types de publication
Journal Article
Langues
eng
Pagination
1065-1079Informations de copyright
© 2022 Kaseb et al.
Déclaration de conflit d'intérêts
A.O.K. has received honoraria from Bayer Health, Bristol Myers Squibb, Eisai, Exelixis, Genentech/Roche, and Merck; has received consulting fees from Bayer Health, Bristol Myers Squibb, Eisai, Exelixis, Genentech/Roche, and Merck; has received institutional research funding from Adaptimmune, Bayer/Onyx, Bristol Myers Squibb, Genentech, Hengrui Pharmaceutical, and Merck; and has received travel, accommodations, and other expense support from Bayer/Onyx, Bristol Myers Squibb, Exelixis, and Merck. Y.G. is an employee of Genentech and holds stock or other ownership interests in F. Hoffmann-La Roche. B.G.Y. has no conflicts of interest to disclose. A.R.A. and S.L. are employees of Genentech and hold stock or other ownership interests in F. Hoffmann-La Roche. E.H. has no conflicts of interest to disclose. H.C.T. has received honoraria from Roche, MSD Merck, Ipsen, and AstraZeneca. W.V. and Y.W. are employees of Genentech and hold stock or other ownership interests in F. Hoffmann-La Roche. The authors report no other conflicts of interest in this work.
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