Home LiteratureArticle Details
PMID: 16314737 Published · ppublish English Clinical Trial Journal Article

Decline in angiogenic factors, such as interleukin-8, indicates response to chemotherapy of metastatic melanoma.

Melanoma research ·Vol. 15 ·No. 6 ·2005-12-00 ·Pages 515-22

Brennecke S, Deichmann M, Naeher H, Kurzen H

Abstract

Serum concentrations of angiogenic factors have been reported to correlate with tumour burden and prognosis in metastatic melanoma. The present study was performed to assess the value of angiogenic factors in serum in indicating response or failure to chemotherapy and immunochemotherapy in stage IV melanoma. Thirty-five patients suffering from stage IV melanoma according to the American Joint Committee on Cancer (AJCC) criteria were included in this prospective study. Before and following chemotherapy or immunochemotherapy, serum levels of vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), platelet-derived growth factor (PDGF-AB), vascular cell adhesion molecule-1 (VCAM-1) and interleukin-8 (IL-8) were measured. Staging examinations following chemotherapy revealed 15 patients with response to therapy (complete response, partial response, stable disease), 14 patients with progressive disease and six patients with mixed response. Patients who responded to therapy showed a significant decrease in the serum level of IL-8 at the time of staging examinations, whereas patients with progressive disease did not. Following chemotherapy, serum concentrations of PDGF-AB had significantly decreased in both patients with response and patients with progressive disease. Comparing the VEGF and bFGF levels of responders and non-responders after a single administration of cytostatics showed significantly lower concentrations in patients with response to therapy. In all patients, a high intra- and inter-individual variability of serum values was observed during application of therapy. It can be concluded that low IL-8 serum levels after chemotherapy indicate response to chemotherapy in stage IV melanoma patients. The persistence of elevated serum levels of VEGF and bFGF following the initial cytostatic administration may help to identify patients resistant to chemotherapy. The distinct variability of serum levels indicates that processes other than tumour angiogenesis also influence the serum concentration of the examined angiogenic factors.

MeSH Terms
Adult Aged Angiogenic Proteins/blood Antineoplastic Combined Chemotherapy Protocols/administration & dosage,therapeutic use Cisplatin/administration & dosage Dacarbazine/administration & dosage Female Fibroblast Growth Factor 2/blood Humans Interferon-alpha/administration & dosage Interleukin-2/administration & dosage Interleukin-8/blood Male Melanoma/blood,drug therapy,pathology,secondary Middle Aged Neoplasm Staging Platelet-Derived Growth Factor/metabolism Prospective Studies Vascular Cell Adhesion Molecule-1/blood Vascular Endothelial Growth Factor A/blood Vindesine/administration & dosage
Chemicals
Angiogenic Proteins Interferon-alpha Interleukin-2 Interleukin-8 Platelet-Derived Growth Factor Vascular Cell Adhesion Molecule-1 Vascular Endothelial Growth Factor A platelet-derived growth factor AB Fibroblast Growth Factor 2 Dacarbazine Cisplatin Vindesine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Brennecke Sabine
Department of Dermatology, University of Heidelberg, Germany. sabine.brennecke@web.de
Deichmann Martin
Naeher Helmut
Kurzen Hjalmar
Supplementary Concepts
DVP protocol (Protocol)
Article Info
Journal
Melanoma research
Abbr.
Melanoma Res
ISSN
0960-8931
Published
2005-12-00
Pages
515-22
Language
English
Region
England
NLM ID
9109623
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com