Are biomarkers correlated with recurrence patterns in patients with resectable gastric adenocarcinoma

被引:9
作者
Li, Gui-Chao [1 ]
Zhang, Zhen [1 ]
Ma, Xue-Jun [1 ]
Gu, Wei-Lie [2 ]
Wang, Ya-Nong [2 ]
Li, Jin [3 ]
机构
[1] Fudan Univ, Dept Radiat Oncol, Shanghai Canc Ctr, Shanghai 200032, Peoples R China
[2] Fudan Univ, Dept Abdominal Surg, Shanghai Canc Ctr, Shanghai 200032, Peoples R China
[3] Fudan Univ, Dept Med Oncol, Gastr Canc Multidisciplinary Treatment Grp, Shanghai 200032, Peoples R China
关键词
Gastric cancer; Recurrence pattern; Bio-marker; Tumor marker; Immunohistochemical (IHC); Prognosis; D2; gastrectomy; GROWTH-FACTOR RECEPTOR; CLINICAL-SIGNIFICANCE; CURATIVE RESECTION; UNITED-STATES; CANCER; SURVIVAL; MANAGEMENT; EXPRESSION; CARCINOMA; MARKER;
D O I
10.1007/s11033-011-0751-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aims of this study are to analyze the failure patterns in radical resected gastric adenocarcinoma, and to evaluate the correlation between recurrence patterns and potentially prognostic factors, including clinical pathological characteristic and biomarkers. Between Jan 2004 and Jun 2006, 84 patients were enrolled into the database analysis, including 8 with clinical stage I, 20 with clinical stage II, 21 with clinical stage IIIA, 22 with clinical stage IIIB and 13 with clinical stage IV, male 61 and female 23. The collected biomarkers including: preoperative tumor markers: CEA, AFP, CA199, CA50, CA72-4 and CA24-2; postoperative immunohistochemical (IHC) markers: Bax, Bcl-2, P27, CyclinD1, TOPO2, MDR, GST-pi, Ki67, epidermal growth factor receptor (EGFR), P21, P53, proliferating cell nuclear antigen (PCNA), C-myc and Neu. Three-year local control rate (LCR), disease-free survival (DFS) and over-all survival (OS) were 66, 61 and 64% respectively. Logistic regression analysis showed cyclinD1 and CEA were correlated with prognosis; cyclinD1, CEA were correlated with loco-regional recurrence; PCNA was correlated with remote metastasis; bcl-2, ki67, c-myc2 and Neu were correlated with lymph node metastasis. The present study indicate that patterns of recurrence are variable and may be associated with specific biomarkers, in addition, high level of CEA and low-expressed of cyclinD1 resulted in poor prognosis.
引用
收藏
页码:399 / 405
页数:7
相关论文
共 32 条
  • [1] Aoyagi Keishiro, 2001, Kurume Medical Journal, V48, P197
  • [2] Patterns of initial recurrence in completely resected gastric adenocarcinoma
    D'Angelica, M
    Gonen, M
    Brennan, MF
    Turnbull, AD
    Bains, M
    Karpeh, MS
    [J]. ANNALS OF SURGERY, 2004, 240 (05) : 808 - 816
  • [3] Clinical significance of the epidermal growth factor receptor and HER2 receptor in resectable gastric cancer
    García, I
    Vizoso, F
    Martín, A
    Sanz, L
    Abdel-Lah, O
    Raigoso, P
    García-Muñiz, JL
    [J]. ANNALS OF SURGICAL ONCOLOGY, 2003, 10 (03) : 234 - 241
  • [4] Clinical significance of epidermal growth factor receptor content in gastric cancer
    García, I
    Vizoso, F
    Andicoechea, A
    Raigoso, P
    Vérez, P
    Alexandre, E
    García-Muñiz, JL
    Allende, MT
    [J]. INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS, 2001, 16 (03) : 183 - 188
  • [5] Goral V, 2007, HEPATO-GASTROENTEROL, V54, P1272
  • [6] Kofuji K, 1993, NIPPON GEKA GAKKAI Z, V4, P8
  • [7] PATTERNS OF FAILURE FOLLOWING CURATIVE RESECTION OF GASTRIC-CARCINOMA
    LANDRY, J
    TEPPER, JE
    WOOD, WC
    MOULTON, EO
    KOERNER, F
    SULLINGER, J
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1990, 19 (06): : 1357 - 1362
  • [8] LEE EY, 1994, ARCH PATHOL LAB MED, V118, P235
  • [9] ARE JAPANESE AND EUROPEAN GASTRIC-CANCER THE SAME BIOLOGICAL ENTITY - AN IMMUNOHISTOCHEMICAL STUDY
    LIVINGSTONE, JI
    YASUI, W
    TAHARA, E
    WASTELL, C
    [J]. BRITISH JOURNAL OF CANCER, 1995, 72 (04) : 976 - 980
  • [10] Targeted killing effects of double CD and TK suicide genes controlled by survivin promoter on gastric cancer cell
    Luo, Xian-Run
    Li, Jian-Sheng
    Niu, Ying
    Miao, Li
    [J]. MOLECULAR BIOLOGY REPORTS, 2011, 38 (02) : 1201 - 1207