A high peripheral microvessel density count correlates with a poor prognosis in pancreatic cancer

被引:51
作者
Takagi, K [1 ]
Takada, T [1 ]
Amano, H [1 ]
机构
[1] Teikyo Univ, Sch Med, Dept Surg, Itabashi Ku, Tokyo 1738605, Japan
关键词
pancreatic cancer; microvessel density; hot-spot method; liver metastasis; factor VIII;
D O I
10.1007/s00535-004-1556-x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background. Microvessel density (MVD) has been shown to be associated with a poor prognosis in gastric, colorectal, breast, and lung cancers. However, there are few positive results in pancreatic cancer. We hypothesized that high counts of MVD, determined by the lumen method as compared with the hot-spot method, would show a significant correlation with a poor prognosis in pancreatic cancer. Methods. Thin slices from the center and periphery of 41 resected pancreatic tumors were immunostained with factor VIII monoclonal antibody. MVD was determined under high magnification by the lumen method, which counts only those structures showing vessel formation positive for factor VIII. The relationship between MVD and clinical and histological variables and the development of liver metastases and survival was assessed with logistic and Cox regression analyses, respectively. Results. Liver metastasis developed in 22 patients (54%) after surgery. Peripheral MVD, as measured by the lumen method, and N-category (TNM classification) were both significantly associated with liver metastasis. Survival rates were 50%, 15%, and 10% for 1, 3, and 5 years, respectively. Poor survival was significantly associated with male sex; high peripheral MVD, as measured by the lumen method; arterial invasion; and T-category ranking (TNM classification). Conclusions. High peripheral MVD, as assessed by the lumen method, is associated with the occurrence of liver metastasis and with a poorer prognosis in pancreatic cancer.
引用
收藏
页码:402 / 408
页数:7
相关论文
共 17 条
  • [1] Vessel counts and vascular endothelial growth factor expression in pancreatic adenocarcinoma
    Ellis, LM
    Takahashi, Y
    Fenoglio, CJ
    Cleary, KR
    Bucana, CD
    Evans, DB
    [J]. EUROPEAN JOURNAL OF CANCER, 1998, 34 (03) : 337 - 340
  • [2] FOLKMAN J, 1971, NEW ENGL J MED, V285, P1182
  • [3] ANGIOGENESIS IN CANCER, VASCULAR, RHEUMATOID AND OTHER DISEASE
    FOLKMAN, J
    [J]. NATURE MEDICINE, 1995, 1 (01) : 27 - 31
  • [4] Expression of two angiogenic factors, vascular endothelial growth factor and platelet-derived endothelial cell growth factor in human pancreatic cancer, and its relationship to angiogenesis
    Fujimoto, K
    Hosotani, R
    Wada, M
    Lee, JU
    Koshiba, T
    Miyamoto, Y
    Tsuji, S
    Nakajima, S
    Doi, R
    Imamura, M
    [J]. EUROPEAN JOURNAL OF CANCER, 1998, 34 (09) : 1439 - 1447
  • [5] Fujioka S, 2001, CANCER, V92, P1788, DOI 10.1002/1097-0142(20011001)92:7<1788::AID-CNCR1695>3.0.CO
  • [6] 2-Z
  • [7] Hall N R, 1992, Surg Oncol, V1, P223, DOI 10.1016/0960-7404(92)90068-V
  • [8] Prognostic significance of angiogenesis in human pancreatic cancer
    Ikeda, N
    Adachi, M
    Taki, T
    Huang, C
    Hashida, H
    Takabayashi, A
    Sho, M
    Nakajima, Y
    Kanehiro, H
    Hisanaga, M
    Nakano, H
    Miyake, M
    [J]. BRITISH JOURNAL OF CANCER, 1999, 79 (9-10) : 1553 - 1563
  • [9] Karademir S, 2000, J Hepatobiliary Pancreat Surg, V7, P489, DOI 10.1007/s005340070020
  • [10] Histologic features of venous invasion, expression of vascular endothelial growth factor and matrix metalloproteinase-2 and matrix metalloproteinase-9, and the relation with liver metastasis in pancreatic cancer
    Nagakawa, Y
    Aoki, T
    Kasuya, K
    Tsuchida, A
    Koyanagi, Y
    [J]. PANCREAS, 2002, 24 (02) : 169 - 178