Neopterin is an independent prognostic variable in females with breast cancer

Citation
C. Murr et al., Neopterin is an independent prognostic variable in females with breast cancer, CLIN CHEM, 45(11), 1999, pp. 1998-2004
Citations number
32
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
CLINICAL CHEMISTRY
ISSN journal
00099147 → ACNP
Volume
45
Issue
11
Year of publication
1999
Pages
1998 - 2004
Database
ISI
SICI code
0009-9147(199911)45:11<1998:NIAIPV>2.0.ZU;2-1
Abstract
Background: Neopterin, produced by human monocytes/macrophages upon stimula tion by interferon-gamma, is a sensitive marker for monitoring Th1-cell imm une response in humans. In malignant diseases, the frequency of increases i n neopterin in the serum and urine of patients depends on tumor stage and t ype. Methods: In a retrospective study comprising 129 females with breast cancer , urinary neopterin/creatinine ratios were measured at the time of diagnosi s. Tumor characteristics were determined concomitantly. Results: Urinary neopterin was increased in 18% of the patients. It did not correlate with tumor size or lymph node status, but it was influenced by t he presence of distant metastases (P <0.05) and by tumor differentiation (P = 0.01). When product-limit estimates were calculated after follow-up for up to 13 years (median follow-up, 56 months), the presence of distant metas tases (P <0.001), neopterin (P <0.001), tumor size (P=0.001), and lymph nod e status (P <0.01) were Significant: predictors of survival. By multivariat e analysis, a combination of the variables presence of distant metastases ( P <0.001), neopterin (P <0.01), and lymph node status (P < 0.05) was found to jointly predict survival. In lymph node-negative patients without distan t metastases, the relative risk of death associated with increased neopteri n concentrations was 2.5 compared with patients with neopterin concentratio ns within the reference interval. Conclusion: Urinary neopterin provides additional prognostic information in patients with breast cancer. (C) 1999 American Association for Clinical Ch emistry.