Tomoda M, Maehara Y, Kakeji Y, Ohno S, Ichiyoshi Y, Sugimachi K
Department of Surgery II, Kyushu University Faculty of Medicine, Fukuoka, Japan.
Cancer. 1999 Jun 1;85(11):2340-6. doi: 10.1002/(sici)1097-0142(19990601)85:11<2340::aid-cncr7>3.0.co;2-i.
The growth pattern of early gastric carcinoma, based on a volumetric analysis, reflects biologic characteristics of the tumor. The authors investigated the microvessel density (MVD), expression of vascular endothelial growth factor (VEGF), and growth patterns in early gastric carcinoma.
Ninety-four tissue specimens resected from patients with early gastric carcinoma invading the submucosal layer were examined. Microvessel quantification was performed immunohistochemically using a monoclonal antibody against factor VIII-related antigen. VEGF expression was studied using an anti-VEGF polyclonal antibody. Growth patterns were defined as follows: Pen A type: expansively penetrating growth; Pen B type: infiltratively penetrating growth; Super type: superficially spreading growth.
The mean MVD was 16.9 (range, 5.2-43.0). MVD was significantly higher in tumors with venous invasion (P<0.01), lymphatic vessel invasion (P<0.05), and lymph node metastases (P<0.05) compared with MVD in tumors without venous or lymphatic vessel invasion or lymph node metastases. The VEGF-positive rate of Pen A type tumors was 66.7% (18 of 27), that Pen B type was 10.0% (1 of 10), that of Super type was 19.4% (6 of 31), and that of the unclassified type was 15.4% (4 of 26). The VEGF-positive rate in patients with Pen A type tumors was significantly higher than that in patients with the other three growth patterns(P<0.01). MVD in patients with Pen A type tumors (25.9+/-9.2) was significantly higher than that in patients with Super type tumors (12.6+/-5.4) (P<0.01). Patients with Pen A type tumors had a poorer prognosis than patients whose tumors had other growth patterns (P<0.05). According to multivariate analysis, VEGF expression and lymphatic vessel invasion were significant prognostic factors.
Pen A type gastric carcinoma tends to secrete VEGF, thus inducing tumor angiogenesis and resulting in venous invasion. Intensive follow-up is necessary for patients with Pen A type tumors, because this tumor type has a greater propensity for hematogenous metastasis.
基于容积分析的早期胃癌生长模式反映了肿瘤的生物学特性。作者研究了早期胃癌的微血管密度(MVD)、血管内皮生长因子(VEGF)的表达及生长模式。
对94例侵犯黏膜下层的早期胃癌患者切除的组织标本进行检查。采用抗VIII因子相关抗原单克隆抗体,通过免疫组织化学方法进行微血管定量分析。使用抗VEGF多克隆抗体研究VEGF表达情况。生长模式定义如下:Pen A型:膨胀性浸润生长;Pen B型:浸润性浸润生长;Super型:浅表扩散生长。
平均MVD为16.9(范围5.2 - 43.0)。与无静脉或淋巴管侵犯及无淋巴结转移的肿瘤相比,有静脉侵犯(P<0.01)、淋巴管侵犯(P<0.05)及淋巴结转移(P<0.05)的肿瘤MVD显著更高。Pen A型肿瘤的VEGF阳性率为66.7%(27例中的18例),Pen B型为10.0%(10例中的1例),Super型为19.4%(31例中的6例),未分类型为15.4%(26例中的4例)。Pen A型肿瘤患者的VEGF阳性率显著高于其他三种生长模式的患者(P<0.01)。Pen A型肿瘤患者的MVD(25.9±9.2)显著高于Super型肿瘤患者(12.6±5.4)(P<0.01)。Pen A型肿瘤患者的预后比肿瘤具有其他生长模式的患者差(P<0.05)。多因素分析显示,VEGF表达和淋巴管侵犯是重要的预后因素。
Pen A型胃癌倾向于分泌VEGF,从而诱导肿瘤血管生成并导致静脉侵犯。对于Pen A型肿瘤患者有必要进行密切随访,因为这种肿瘤类型有更高的血行转移倾向。