Progress and challenges in screening for early detection of ovarian cancer

被引:331
作者
Jacobs, IJ [1 ]
Menon, U [1 ]
机构
[1] Barts & London Queen Marys Sch Med & Dent, Inst Canc, Dept Gynecol Oncol, London EC1M 6GR, England
基金
英国医学研究理事会;
关键词
D O I
10.1074/mcp.R400006-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Ovarian cancer is characterize by few early symptoms, presentation at an advanced stage, and poor survival. As a result, it is the most frequent cause of death from gynecological cancer. During the last decade, a research effort has been directed toward improving outcomes for ovarian cancer by screening for preclinical, early stage disease using both imaging techniques and serum markers. Numerous biomarkers have shown potential in samples from clinically diagnosed ovarian cancer patients, but few have been thoroughly assessed in preclinical disease and screening. The most thoroughly investigated biomarker in ovarian cancer screening is CA125. Prospective studies have demonstrated that both CA125 and transvaginal ultrasound can detect a significant proportion of preclinical ovarian cancers, and refinements in interpretation of results have improved sensitivity and reduced the false-positive rate of screening. There is preliminary evidence that screening can improve survival, but the impact of screening on mortality from ovarian cancer is still unclear. Prospective studies of screening are in progress in both the general population and high-risk population, including the United Kingdom Collaborative Trial of Ovarian Cancer Screening (UKC-TOCS), a randomized trial involving 200,000 postmenopausal women designed to document the impact of screening on mortality. Recent advances in technology for the study of the serum proteome offer exciting opportunities for the identification of novel biomarkers or patterns of markers that will have greater sensitivity and lead time for preclinical disease than CA125. Considerable interest and controversy has been generated by initial results utilizing surface-enhanced laser desorption/ionization (SELDI) in ovarian cancer. There are challenging issues related to the design of studies to evaluate SELDI and other proteomic technology, as well as the reproducibility, sensitivity, and specificity of this new technology. Large serum banks such as that assembled in UKCTOCS, which contain preclinical samples from patients who later developed ovarian cancer and other disorders, provide a unique resource for carefully designed studies of proteomic technology. There is a sound basis for optimism that further developments in serum proteomic analysis will provide powerful methods for screening in ovarian cancer and many other diseases.
引用
收藏
页码:355 / 366
页数:12
相关论文
共 111 条
  • [1] Adam BL, 2002, CANCER RES, V62, P3609
  • [2] Combined approach for the early detection of ovarian cancer in asymptomatic women
    Adonakis, GL
    Paraskevaidis, E
    Tsiga, S
    Seferiadis, K
    Lolis, DE
    [J]. EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 1996, 65 (02): : 221 - 225
  • [3] [Anonymous], 2003, J Clin Oncol, DOI [10.1200/jco.2003.02.955, DOI 10.1200/JCO.2003.02.955, DOI 10.1200/JC0.2003.02.955, 10.1200/JCO.2003.02.955]
  • [4] Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history:: A combined analysis of 22 studies
    Antoniou, A
    Pharoah, PDP
    Narod, S
    Risch, HA
    Eyfjord, JE
    Hopper, JL
    Loman, N
    Olsson, H
    Johannsson, O
    Borg, Å
    Pasini, B
    Radice, P
    Manoukian, S
    Eccles, DM
    Tang, N
    Olah, E
    Anton-Culver, H
    Warner, E
    Lubinski, J
    Gronwald, J
    Gorski, B
    Tulinius, H
    Thorlacius, S
    Eerola, H
    Nevanlinna, H
    Syrjäkoski, K
    Kallioniemi, OP
    Thompson, D
    Evans, C
    Peto, J
    Lalloo, F
    Evans, DG
    Easton, DF
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (05) : 1117 - 1130
  • [5] The malignant potential of small cystic ovarian tumors in women over 50 years of age
    Bailey, CL
    Ueland, FR
    Land, GL
    DePriest, PD
    Gallion, HH
    Kryscio, RJ
    van Nagell, JR
    [J]. GYNECOLOGIC ONCOLOGY, 1998, 69 (01) : 3 - 7
  • [6] A RADIOIMMUNOASSAY USING A MONOCLONAL-ANTIBODY TO MONITOR THE COURSE OF EPITHELIAL OVARIAN-CANCER
    BAST, RC
    KLUG, TL
    STJOHN, E
    JENISON, E
    NILOFF, JM
    LAZARUS, H
    BERKOWITZ, RS
    LEAVITT, T
    GRIFFITHS, CT
    PARKER, L
    ZURAWSKI, VR
    KNAPP, RC
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1983, 309 (15) : 883 - 887
  • [7] REACTIVITY OF A MONOCLONAL-ANTIBODY WITH HUMAN OVARIAN-CARCINOMA
    BAST, RC
    FEENEY, M
    LAZARUS, H
    NADLER, LM
    COLVIN, RB
    KNAPP, RC
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1981, 68 (05) : 1331 - 1337
  • [8] BELINSON JL, 1995, CLEV CLIN J MED, V62, P129
  • [9] THE POTENTIAL ROLE OF SERUM CA-125 IN AN ULTRASOUND-BASED SCREENING-PROGRAM FOR FAMILIAL OVARIAN-CANCER
    BOURNE, TH
    CAMPBELL, S
    REYNOLDS, K
    HAMPSON, J
    BHATT, L
    CRAYFORD, TJB
    WHITEHEAD, MI
    COLLINS, WP
    [J]. GYNECOLOGIC ONCOLOGY, 1994, 52 (03) : 379 - 385
  • [10] SCREENING FOR EARLY FAMILIAL OVARIAN-CANCER WITH TRANSVAGINAL ULTRASONOGRAPHY AND COLOR BLOOD-FLOW IMAGING
    BOURNE, TH
    CAMPBELL, S
    REYNOLDS, KM
    WHITEHEAD, MI
    HAMPSON, J
    ROYSTON, P
    CRAYFORD, TJB
    COLLINS, WP
    [J]. BRITISH MEDICAL JOURNAL, 1993, 306 (6884) : 1025 - 1029