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通过抗细胞角蛋白抗体CAM5.2检测发现,黏膜下结直肠癌最深浸润边缘的肿瘤芽生与淋巴结转移相关。

Tumour budding at the deepest invasive margin correlates with lymph node metastasis in submucosal colorectal cancer detected by anticytokeratin antibody CAM5.2.

作者信息

Kazama S, Watanabe T, Ajioka Y, Kanazawa T, Nagawa H

机构信息

Department of Surgery, Division of Surgical Oncology, Faculty of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-Ku, Tokyo 113-8655, Japan.

出版信息

Br J Cancer. 2006 Jan 30;94(2):293-8. doi: 10.1038/sj.bjc.6602927.

Abstract

In the past few years, tumour budding at the invasive margin has been reported as a new risk factor for lymph node metastasis in advanced colorectal cancers, but it is sometimes difficult to detect tumour budding in submucosal colorectal cancer by haematoxylin and eosin staining. We immunohistochemically examined tumour budding at the deepest invasive margin of 56 surgically resected submucosal colorectal carcinomas using anticytokeratin antibody CAM5.2, furthermore checked by AE1/AE3, and determined the relation between tumour budding and clinicopathological factors. Moreover, we used the monoclonal antibody D2-40 for immunohistochemistry to detect lymphatic involvement. Tumour budding was detected in 42 cases (75.0%), and the budding-positive group showed a significantly higher rate of lymph node metastasis (including isolated tumour cells) (16/42 vs 0/14; P=0.004) than the budding-negative group. The sensitivity and negative predictive value of tumour budding alone for lymph node metastasis were superior to those of lymphatic invasion alone. Furthermore, the specificity and positive predictive value of the combination of either lymphatic invasion or tumour budding were superior to those of lymphatic invasion alone. Tumour budding detected immunohistochemically by using CAM5.2 is a newly found risk factor for lymph node metastasis and may help to avoid oversurgery in the future.

摘要

在过去几年中,侵袭边缘的肿瘤芽生已被报道为晚期结直肠癌淋巴结转移的一个新的危险因素,但有时通过苏木精和伊红染色难以检测到黏膜下结直肠癌的肿瘤芽生。我们使用抗细胞角蛋白抗体CAM5.2对56例手术切除的黏膜下结直肠癌的最深侵袭边缘进行免疫组织化学检查肿瘤芽生,进一步用AE1/AE3检查,并确定肿瘤芽生与临床病理因素之间的关系。此外,我们使用单克隆抗体D2-40进行免疫组织化学检测淋巴管侵犯情况。42例(75.0%)检测到肿瘤芽生,芽生阳性组的淋巴结转移(包括孤立肿瘤细胞)率(16/42 vs 0/14;P=0.004)显著高于芽生阴性组。单独肿瘤芽生对淋巴结转移的敏感性和阴性预测值优于单独淋巴管侵犯。此外,淋巴管侵犯或肿瘤芽生联合检测的特异性和阳性预测值优于单独淋巴管侵犯。通过使用CAM5.2免疫组织化学检测到的肿瘤芽生是新发现的淋巴结转移危险因素,可能有助于未来避免过度手术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffdb/2361114/5a0e07bd023a/94-6602927f1.jpg

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