Natsugoe S, Mueller J, Stein H J, Feith M, Höfler H, Siewert J R
Department of Surgery, Technical University of Munich, Germany.
Cancer. 1998 Sep 1;83(5):858-66.
The purpose of this study was to investigate micrometastasis (MM) and tumor cell microinvolvement (TCM) in the regional lymph nodes of patients with esophageal squamous cell carcinoma (SCC).
MM was defined as individual tumor cells or tumor cell clusters <0.5 mm in greatest dimension with a surrounding stromal reaction. TCM was defined as individual tumor cells or tumor cell clusters without a surrounding stromal reaction. One thousand nine hundred and fifty-four lymph nodes were dissected from 69 complete (R0) resection specimens of TNM classified pT1-3, pN0 or pN1, and M0 esophageal SCC. These lymph nodes were examined immunohistochemically using the monoclonal antibody cocktail AE1/AE3 for cytokeratins. The primary tumors were immunostained with an anti-E-cadherin monoclonal antibody.
MM +/- TCM was found in 13 cases (31.7%) and TCM alone in 2 cases (4.9%) of the 41 pN0 cases. The pN0 patients with MM (but not TCM) had the same shorter survival as the original pN1 cases (P < 0.05). Of the 69 primary tumors, 49 (71.0%) had reduced or negative E-cadherin expression that showed a correlation with the occurrence of lymph node metastases (original pN1), MM, and TCM, but not prognosis.
The results of the current study show that, in SCC of the esophagus, MM, but not TCM, in the regional lymph nodes is prognostically equivalent to metastasis and should be examined by immunohistochemistry to classify these cases correctly as pN1.
本研究旨在调查食管鳞状细胞癌(SCC)患者区域淋巴结中的微转移(MM)和肿瘤细胞微浸润(TCM)情况。
MM定义为最大直径<0.5 mm且伴有周围基质反应的单个肿瘤细胞或肿瘤细胞簇。TCM定义为无周围基质反应的单个肿瘤细胞或肿瘤细胞簇。从69例TNM分期为pT1 - 3、pN0或pN1且M0的食管SCC完整(R0)切除标本中解剖出1954个淋巴结。使用细胞角蛋白单克隆抗体混合物AE1/AE3对这些淋巴结进行免疫组织化学检查。原发性肿瘤用抗E - 钙黏蛋白单克隆抗体进行免疫染色。
在41例pN0病例中,13例(31.7%)发现有MM ± TCM,2例(4.9%)仅发现有TCM。有MM(但无TCM)的pN0患者与原pN1病例的生存期同样较短(P < 0.05)。在69例原发性肿瘤中,49例(71.0%)E - 钙黏蛋白表达降低或呈阴性,这与淋巴结转移(原pN1)、MM和TCM的发生相关,但与预后无关。
本研究结果表明,在食管SCC中,区域淋巴结中的MM而非TCM在预后方面与转移相当,应通过免疫组织化学检查以将这些病例正确分类为pN1。