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[肺肠型腺癌的研究进展]

[Progress in pulmonary enteric adenocarcinoma].

作者信息

Zuo Y, Bai H, Ying J M, Wang J

机构信息

Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.

Department of Pathology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.

出版信息

Zhonghua Zhong Liu Za Zhi. 2022 Apr 23;44(4):321-325. doi: 10.3760/cma.j.cn112152-20200818-00753.

Abstract

Pulmonary enteric adenocarcinoma (PEAC), as a rare histologic subtype of primary lung adenocarcinoma, is defined as an adenocarcinoma in which the enteric component exceeds 50%. It is named after its shared morphological and immunohistochemical features with colorectal cancer. While with such similarity, the differential diagnosis of PEAC and lung metastatic colorectal cancer is a great challenge in the clinic. PEAC may originate from the intestinal metaplasia of respiratory basal cells stimulated by risk factors such as smoking. Current studies have found that is a relatively high-frequency mutation gene, and other driver gene mutations are rare. In terms of immunohistochemistry, in pulmonary enteric adenocarcinoma, the positive rate was 88.2% (149/169) for CK7, 78.1% (132/169) for CDX2, 48.2% (82/170) for CK20 and 38.8% (66/170) for TTF1. As for clinical features, the average age of onset for pulmonary enteric adenocarcinoma was 62 years, male patients accounted for 56.5% (35/62), smokers accounted for 78.8% (41/52), and 41.4% (24/58) of the primary lesion was located in the upper lobe of the right lung. In terms of treatment, conventional non-small cell lung cancer (NSCLC) regimens rather than colorectal cancer regimens are now recommended. There is still an urgent need for more basic and clinical research, in-depth exploration of its molecular feature and pathogenesis from the level of omics and other aspects, to help diagnosis and differential diagnosis, and find the optimal chemotherapy regimen, possibly effective targeted therapy and even immunotherapy.

摘要

肺肠型腺癌(PEAC)作为原发性肺腺癌的一种罕见组织学亚型,被定义为肠型成分超过50%的腺癌。它因其与结直肠癌共有的形态学和免疫组化特征而得名。尽管有如此相似性,但PEAC与肺转移性结直肠癌的鉴别诊断在临床上仍是一项巨大挑战。PEAC可能起源于吸烟等危险因素刺激的呼吸基底细胞的肠化生。目前的研究发现, 是一个相对高频的突变基因,其他驱动基因突变罕见。在免疫组化方面,在肺肠型腺癌中,CK7的阳性率为88.2%(149/169),CDX2为78.1%(132/169),CK20为48.2%(82/170),TTF1为38.8%(66/170)。至于临床特征,肺肠型腺癌的平均发病年龄为62岁,男性患者占56.5%(35/62),吸烟者占78.8%(41/52),41.4%(24/58)的原发灶位于右肺上叶。在治疗方面,目前推荐采用传统的非小细胞肺癌(NSCLC)方案而非结直肠癌方案。仍迫切需要更多的基础和临床研究,从组学等层面深入探索其分子特征和发病机制,以辅助诊断和鉴别诊断,并找到最佳化疗方案、可能有效的靶向治疗甚至免疫治疗。

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