PMID- 15221995 OWN - NLM STAT- MEDLINE DCOM- 20040716 LR - 20151119 IS - 0008-543X (Print) IS - 0008-543X (Linking) VI - 101 IP - 1 DP - 2004 Jul 1 TI - Association between serum levels of soluble tumor necrosis factor receptors/CA 125 and disease progression in patients with epithelial ovarian malignancy: a gynecologic oncology group study. PG - 106-15 AB - BACKGROUND: A prospective study was undertaken within the Gynecologic Oncology Group to determine whether serum levels of soluble tumor necrosis factor receptors I (sTNFR-I) and II (sTNFR-II), alone or in combination with CA 125, were associated with clinicopathologic characteristics or outcome in patients with epithelial ovarian malignancies. METHODS: Quantitative immunoassays were performed on valid pretreatment serum specimens obtained from patients with epithelial ovarian malignancies to assess levels of sTNFR-I, sTNFR-II, and CA 125. The authors then analyzed the results of these immunoassays for potential correlations with clinicopathologic characteristics and outcome. RESULTS: The median age of the 139 women evaluated was 59 years. Seventy-eight percent had Stage III or IV disease, and 58% had serous carcinomas. sTNFR-II was associated with age (P = 0.013), and CA 125 was associated with histologic subtype (P = 0.0009). In addition, sTNFR-I (P = 0.037) and CA 125 (P < 0.0001) were associated with extent of disease. After adjusting for patient age, histologic subtype, and extent of disease, all three biomarkers were predictive of progression-free survival, but not overall survival, when the combination was included in the model. The authors observed a 51% reduction (hazard ratio [HR], 0.49; 95% confidence interval [CI], 0.24-0.99), a 2.9-fold increase (HR, 2.87; 95% CI, 1.15-7.20), and a 22% increase (HR, 1.22; 95% CI, 0.99-1.51) in the risk of progression for each unit increase in the log-transformed levels of sTNFR-I, sTNFR-II, and CA 125, respectively. CONCLUSIONS: The observations made in the current study-that among patients with low or high CA 125 levels, those with high sTNFR-I levels and low sTNFR-II levels had the lowest risk, that patients with low-low or high-high sTNFR-I and sTNFR-II levels, respectively, had an intermediate risk, and that patients with low sTNFR-I levels and high sTNFR-II levels had the highest risk of progression-suggested the potential value of simultaneous assessment of all three biomarkers in patients with epithelial ovarian malignancies. CI - Copyright 2004 American Cancer Society. FAU - Burger, Robert A AU - Burger RA AD - Department of Obstetrics and Gynecology, University of California-Irvine Medical Center, Orange, CA, USA. FAU - Darcy, Kathleen M AU - Darcy KM FAU - DiSaia, Philip J AU - DiSaia PJ FAU - Monk, Bradley J AU - Monk BJ FAU - Grosen, Elizabeth A AU - Grosen EA FAU - Gatanaga, Tetsuya AU - Gatanaga T FAU - Granger, Gale A AU - Granger GA FAU - Wang, Jianmin AU - Wang J FAU - Tian, Chunqiao AU - Tian C FAU - Hanjani, Parviz AU - Hanjani P FAU - Cohn, David E AU - Cohn DE LA - eng GR - CA 27469/CA/NCI NIH HHS/United States GR - CA 37517/CA/NCI NIH HHS/United States PT - Clinical Trial PT - Clinical Trial, Phase III PT - Comparative Study PT - Historical Article PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - Cancer JT - Cancer JID - 0374236 RN - 0 (Biomarkers, Tumor) RN - 0 (CA-125 Antigen) RN - 0 (Immunoglobulin G) RN - 0 (Receptors, Tumor Necrosis Factor) RN - OP401G7OJC (Etanercept) SB - IM MH - Aged MH - Biomarkers, Tumor/blood MH - CA-125 Antigen/*blood MH - Enzyme-Linked Immunosorbent Assay MH - Etanercept MH - Female MH - History, 16th Century MH - Humans MH - Immunoglobulin G/*blood MH - Middle Aged MH - Neoplasms, Glandular and Epithelial/*blood/mortality/pathology MH - Ovarian Neoplasms/*blood/mortality/pathology MH - Receptors, Tumor Necrosis Factor/*blood EDAT- 2004/06/29 05:00 MHDA- 2004/07/17 05:00 CRDT- 2004/06/29 05:00 PHST- 2004/06/29 05:00 [pubmed] PHST- 2004/07/17 05:00 [medline] PHST- 2004/06/29 05:00 [entrez] AID - 10.1002/cncr.20314 [doi] PST - ppublish SO - Cancer. 2004 Jul 1;101(1):106-15. doi: 10.1002/cncr.20314.