Serum bFGF (basic fibroblast growth factor) and CA 15.3 in the monitoring of breast cancer patients

Citation
Mf. Pichon et al., Serum bFGF (basic fibroblast growth factor) and CA 15.3 in the monitoring of breast cancer patients, ANTICANC R, 20(2B), 2000, pp. 1189-1194
Citations number
23
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
ISSN journal
02507005 → ACNP
Volume
20
Issue
2B
Year of publication
2000
Pages
1189 - 1194
Database
ISI
SICI code
0250-7005(200003/04)20:2B<1189:SB(FGF>2.0.ZU;2-L
Abstract
Background. Basic fibroblast growth factor (bFGF) is a potent angiogenetic factor which may influence breast cancer evolution. Materials and methods. Serum bFGF, (cut-off 10 pg/ml), was assayed in 166 breast cancer patients a t all stages and compared with CA 15.3. Results. In 99 pre-treatment (PT) s era, 39/99 (39.4 %) were bFGF positive, 9/99 (9.1 %) CA 15.3 positive (>30 U/ml), and not correlated No correlations were found between bFGF and age, menopausal status, TNM or pTNM, histology, SBR grading or steroid receptors . A post-operative decline in bFGF positivity, from 30.8 to 7.7 % (n=39), w as observed. An abnormal CA 15.3 after primary treatment (n=2/39) was of ba d prognosis (P<0.0001), whereas positive bFGF (n=3/39) had no univariate pr ognostic value (median follow-up 5.5 years). During follow-up, positive bFG F was recorded in 6/92 (6.5%) disease-free patients (DFS), 13/15 (86.7%) re gressions, 8/16 (50.0%) stable disease, and 46/67 (68.7%) progressive disea se (significant differences between PT or DFS and post recurrence levels (P <0.001), and between relapse before and after treatment (P=0.002)). Conclus ion. Serum bFGF is more often elevated before treatment or after relapse th an in DFS, and rises under systemic treatments. Its pattern of variations d oes not add to CA 15.3 for breast cancer monitoring.