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Use of the CA 125 Algorithm for the Early Detection of Ovarian Cancer in Low Risk Women
RECRUITINGN/ASponsored by M.D. Anderson Cancer Center
Actively Recruiting
PhaseN/A
SponsorM.D. Anderson Cancer Center
Started2001-07-02
Est. completion2028-11-30
Eligibility
Age50 Years – 74 Years
SexFEMALE
Healthy vol.Accepted
Locations11 sites
View on ClinicalTrials.gov →
NCT00539162
Summary
The goal of this clinical research study is to evaluate a method involving 4 blood tests called CA-125, HE4, HE4 antigen autoantibody complexes, and osteopontin that may be helpful in the early detection of ovarian cancer in women who are at low risk.
Eligibility
Age: 50 Years – 74 YearsSex: FEMALEHealthy volunteers accepted
Inclusion Criteria: 1. Female, \>/= 50 years old or less than 75 years old. 2. Postmenopausal (\>/= 12 months amenorrhea). 3. Have at least one ovary. 4. Cancer-free and have not received any chemotherapy or radiation therapy for \>/=12 months prior to enrolling on this study. 5. Willingness to return for CA 125 blood tests annually or earlier if indicated. 6. Willingness to return to undergo transvaginal ultrasound if indicated. 7. Women need to provide the name of a gynecologist or qualified healthcare professional willing to provide appropriate follow-up care if indicated Exclusion Criteria: 1. Female: Less than 50 years old or older than 75 years at the time of enrollment. 2. Psychiatric or psychological or other conditions which prevent a fully informed consent. 3. Prior removal of both ovaries. 4. Active non-ovarian malignancy. 5. Women who have a history of non-ovarian malignancy will be eligible if they have no persistent or recurrent disease and have not received treatment for \>12 months. If they are on SERMS (i.e. tamoxifen or aromatase inhibitors) they will not be excluded. Women maybe undergoing or have had treatment \<12 months prior to study entry for basal cell carcinoma only. 6. High risk for ovarian cancer due to familial predisposition as defined by the following: a. Known mutation in BRCA1 of BRCA2. b. Two 1st or 2nd degree relatives of same lineage who have: two ovarian cancers; one ovarian cancer \& one pre-menopausal breast cancer; two pre-menopausal breast cancers; one pre-menopausal \& one post-menopausal breast cancer. (These conditions can also be met using the patient and one 1st or 2nd degree female relative.) c. Ashkenazi Jewish descent with one 1st degree or two 2nd degree relatives with pre-menopausal breast or ovarian cancer or participant has had pre-menopausal breast cancer. d. 1st or 2nd degree male relative with breast cancer diagnosed at any age. (First degree relative defined as children, siblings and parents. Second degree relative defined as half-siblings, aunts, uncles, nieces, nephews, grandparents, and grandchildren.) 7. Hereditary Nonpolyposis Colorectal Cancer (HNPCC)/Lynch Syndrome: known genetic mutation, presumed HNPCC carrier, Amsterdam criteria.
Conditions2
CancerOvarian Cancer
Locations11 sites
Sylvester Comprehensive Cancer Center, Univ of Miami Miller School of Medicine
Miami, Florida, 33136
Brian Slomovitz, MD
John Stoddard Cancer Center
Des Moines, Iowa, 50309
Carol G. Simon Cancer Center / Atlantic Health
Morristown, New Jersey, 07962
University of Rochester Medical Center
Rochester, New York, 14642
Richard Moore, MD
University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, 73104
Laura Holman, MD
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Actively Recruiting
PhaseN/A
SponsorM.D. Anderson Cancer Center
Started2001-07-02
Est. completion2028-11-30
Eligibility
Age50 Years – 74 Years
SexFEMALE
Healthy vol.Accepted
Locations11 sites
View on ClinicalTrials.gov →
NCT00539162