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1.
Int J Gynecol Cancer ; 24(7): 1195-205, 2014 Sep.
Article in English | MEDLINE | ID: mdl-25101855

ABSTRACT

BACKGROUND: Triage of patients with ovarian cancer to primary debulking surgery (PDS) or neoadjuvant chemotherapy (NACT) is challenging. In Denmark, the use of NACT has increased, but substantial differences in the use of NACT or PDS exist among centers. We aimed to characterize the differences between intended and actual first-line treatments in addition to the differences in the triage process among the centers and to evaluate the different diagnostic modalities and the clinical aspects' influence in the triage process. MATERIALS AND METHODS: From 4 centers, forms containing data about the diagnostic process and intended treatment were prospectively collected and merged with data from the Danish Gynecological Cancer Database and medical records. RESULTS: Of the 671 completed forms, 540 patients had stage IIIC or IV epithelial ovarian cancer. Of the 238 (44%) referred to PDS, 91% received PDS and 4% never had debulking surgery. Of the 288 patients (53%) referred to NACT, 44% were never debulked. Fourteen patients (3%) were referred to palliative treatment. The use of different imaging modalities, diagnostic laparoscopy, and laparotomy varied significantly among the centers. Diagnostic surgical procedures were considered to be most influential in the triage process. Regardless of the intended first-line treatment or center, the tumor size and dissemination was the most influential clinical aspect. CONCLUSIONS: In Denmark, substantial differences exist between intended and actual first-line treatments as well as in the diagnostic process and use of NACT, calling for further discussion on diagnostic strategy and therapeutically approach for patients with advanced ovarian cancer.


Subject(s)
Diagnostic Techniques, Obstetrical and Gynecological/statistics & numerical data , Intention , Neoadjuvant Therapy/statistics & numerical data , Neoplasms, Glandular and Epithelial , Ovarian Neoplasms , Practice Patterns, Physicians'/statistics & numerical data , Aged , Antineoplastic Agents/therapeutic use , Carcinoma, Ovarian Epithelial , Denmark/epidemiology , Disease Progression , Female , Gynecologic Surgical Procedures/statistics & numerical data , Humans , Middle Aged , Neoadjuvant Therapy/methods , Neoplasms, Glandular and Epithelial/diagnosis , Neoplasms, Glandular and Epithelial/drug therapy , Neoplasms, Glandular and Epithelial/epidemiology , Neoplasms, Glandular and Epithelial/surgery , Ovarian Neoplasms/diagnosis , Ovarian Neoplasms/drug therapy , Ovarian Neoplasms/epidemiology , Ovarian Neoplasms/surgery , Triage/methods
3.
Anticancer Res ; 32(9): 3817-25, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22993324

ABSTRACT

BACKGROUND: New biological markers with predictive or prognostic value are highly warranted in the treatment of ovarian cancer. The platelet-derived growth factor (PDGF) system and fibroblast growth factor (FGF) system are important components in tumor growth and angiogenesis. MATERIALS AND METHODS: Pre-surgery peripheral blood samples were collected consecutively from 213 patients (42 with normal ovaries, 54 with benign, 21 with borderline, and 96 with malignant ovarian tumors) undergoing surgery for an untreated pelvic mass. Serum PDGF-AA, PDGF-BB, and FGF2 were quantified on a Luminex analyzer. RESULTS: Median PDGF-AA, PDGF-BB, and FGF2 levels were higher in patients with ovarian cancer than in those with borderline tumors, and normal ovaries, and PDGF-BB and FGF2 were also higher as compared to patients with benign tumors. PDGF-AA and PDGF-BB were associated with FIGO stage and residual tumor and PDGF-BB was associated with histological subtype. CONCLUSION: PDGF-AA, PDGF-BB, and FGF2 are up-regulated in ovarian cancer and levels of serum PDGF-AA and PDGF-BB seem to be associated with stage and residual tumor in ovarian cancer.


Subject(s)
Biomarkers, Tumor/blood , Fibroblast Growth Factor 2/blood , Ovarian Neoplasms/blood , Platelet-Derived Growth Factor/metabolism , Proto-Oncogene Proteins c-sis/blood , Becaplermin , Female , Humans , Middle Aged , Neoplasm Staging , Ovarian Neoplasms/pathology , Up-Regulation
4.
Gynecol Oncol ; 97(2): 410-2, 2005 May.
Article in English | MEDLINE | ID: mdl-15863138

ABSTRACT

OBJECTIVES: CA 125 is a tumor marker widely used to diagnose, monitor, and follow-up women with epithelial ovarian cancer, as the marker is well related to the amount of vital tumor cells. However, CA 125 before the operation or during the first 2 courses of chemotherapy does not provide enough information concerning survival to serve as a prognostic marker. The present investigation was inspired by studies describing a paradoxical increase of tumor markers (CEA, CA 125, and CA 15-3) in the days after chemotherapy of women with breast cancer. If CA 125 increases within days after chemotherapy, the increase may be caused by death of the cancer cells. It was therefore speculated if a CA 125 spike may serve as an early prognostic parameter. The aim of the present investigation was to evaluate if CA 125 increases within days after the first course of chemotherapy of women with ovarian cancer. PATIENTS: Twenty women with epithelial ovarian cancer were included in the study. CA 125 was measured in each woman on day 0 (the day of, but before initiation of chemotherapy) and 1, 3, 5, 7, 9, and 14 days after chemotherapy. RESULTS: One woman was excluded due to normal CA 125 values. The remaining 19 patients displayed a significant decrease in CA 125 during the 14-day period after chemotherapy. CONCLUSION: In the present study, no chemotherapy-induced increase of CA 125 within the first 14 days after chemotherapy could be demonstrated.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , CA-125 Antigen/blood , Ovarian Neoplasms/blood , Ovarian Neoplasms/drug therapy , Adult , Aged , Carboplatin/administration & dosage , Cisplatin/administration & dosage , Cyclophosphamide/administration & dosage , Doxorubicin/administration & dosage , Epirubicin/administration & dosage , Epithelial Cells/pathology , Female , Humans , Middle Aged , Paclitaxel/administration & dosage
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