Author | Year | Patients | Treatment | Factors | Samples collected | Results |
---|---|---|---|---|---|---|
Carpizo et al. [28] | 2014 | n = 15 CRCLM | 90Y-RE | VEGF, Ang-2, b-FGF, PDGF-BB, TSP-1, follistatin, leptin, IL-8 | Baseline | * Transient increases in many angiogenic cytokines * Some changes associated with worse OS |
n = 7 HCC | 6 h, and 3, 14, 30, 60, 90 and 120 days of follow-up | |||||
Korse et al. [27] | 2011 | n = 12 NET | HAE | VEGF, ET-1, proET-1 | Baseline | * VEGF and proET-1 showed temporarily increase after treatment |
1, 2, 3, 4, 5, 6, 7 and 8 days of follow-up | ||||||
Sergio et al. [10] | 2008 | n = 71 HCC | TACE | VEGF, b-FGF, uPA | Baseline | * VEGF levels were higher in non-responders at 1-month follow-up |
3 and 30 days of follow-up | * Below-median VEGF levels predicted a longer survival | |||||
Shim et al. [26] | 2008 | n = 147 HCC | TACE | VEGF | Baseline | * High increment in serum VEGF level 1–2 days post treatment was associated with distant metastasis and unfavourable outcomes |
1–2 and 30 days of follow-up | ||||||
Li et al. [8] | 2004 | n = 45 HCC | TACE | VEGF | Baseline | * A high pre-treatment VEGF level was associated with poor response |
n = 20 benign disease | 1, 3, 7 and 30 days of follow-up | |||||
n = 17 healthy controls | * VEGF levels increased significantly on the first day post treatment | |||||
Suzuki et al. [9] | 1999 | n = 38 HCC | TAE | VEGF, HGF | Baseline | * No significant alterations in HGF levels |
1, 3 and 7 days of follow-up | * VEGF levels increased significantly at 7 days post treatment |