Malignant effusions: From diagnosis to biology

被引:67
作者
Davidson, B [1 ]
机构
[1] Univ Oslo, Norwegian Radium Hosp, Dept Pathol, N-0310 Oslo, Norway
关键词
effusions; cancer; disease progression; prognosis;
D O I
10.1002/dc.20133
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Serous effusions are a frequently encountered clinical manifestation of metastatic disease, with breast, ovarian, and lung carcinomas and malignant mesothelioma (MM) leading the list. Recently, extensive research has resulted in expansion of the antibody panel that is available for effusion diagnosis, thereby reducing the risk for error. Despite this progress, relatively little has been done in way of understanding the biology of cancer cells in effusions, especially those of nonovarian origin. The diagnosis of a malignant effusion signifies disease progression and is associated with a worse prognosis regardless of the tumor site of origin. However, survival is much more variable with ovarian cancer compared with other tumors. Furthermore, cancer cells of different origins differ considerably in their biology and have unique phenotypic and genotypic characteristics. This review summarizes the current knowledge in this field and presents a model for the study of tumor metastasis and disease progression, through large comparative studies of malignant cells in effusions, primary tumors, and solid metastases. The case also is made,for potential applications of this rapidly evolving body of knowledge in the diagnosis, classification, and prediction of biological behavior of processes resulting in cryptic effusions at the clinical level. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:246 / 254
页数:9
相关论文
共 99 条
  • [1] Abendstein B, 2000, CANCER, V88, P1432, DOI 10.1002/(SICI)1097-0142(20000315)88:6<1432::AID-CNCR22>3.0.CO
  • [2] 2-8
  • [3] Prognostic factors of stage IV epithelial ovarian cancer: A multicenter retrospective study
    Akahira, JI
    Yoshikawa, H
    Shimizu, Y
    Tsunematsu, R
    Hirakawa, T
    Kuramoto, H
    Shiromizu, K
    Kuzuya, K
    Kamura, T
    Kikuchi, Y
    Kodama, S
    Yamamoto, K
    Sato, S
    [J]. GYNECOLOGIC ONCOLOGY, 2001, 81 (03) : 398 - 403
  • [4] Chemokines: key players in cancer
    Arya, M
    Patel, HRH
    Williamson, M
    [J]. CURRENT MEDICAL RESEARCH AND OPINION, 2003, 19 (06) : 557 - 564
  • [5] NEUROTROPHIC FACTORS AND THEIR RECEPTORS
    BARBACID, M
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (02) : 148 - 155
  • [6] Bedrossian CWM, 1998, DIAGN CYTOPATHOL, V19, P131, DOI 10.1002/(SICI)1097-0339(199808)19:2<131::AID-DC14>3.0.CO
  • [7] 2-G
  • [8] Bedrossian CWM, 1994, Malignant Effusions: A Multimodal Approach to Cytologic Diagnosis
  • [9] Inflammatory cells, cytokines and chemokines in breast cancer progression: reciprocal tumor-microenvironment interactions
    Ben-Baruch, A
    [J]. BREAST CANCER RESEARCH, 2003, 5 (01) : 31 - 36
  • [10] EXPRESSION OF VASCULAR ENDOTHELIAL GROWTH-FACTOR AND ITS RECEPTORS FLT AND KDR IN OVARIAN-CARCINOMA
    BOOCOCK, CA
    CHARNOCKJONES, DS
    SHARKEY, AM
    MCLAREN, J
    BARKER, PJ
    WRIGHT, KA
    TWENTYMAN, PR
    SMITH, SK
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (07): : 506 - 516