Department of Respiratory Medicine, Kumamoto Chuo Hospital, Kumamoto-shi, Kumamoto 860-8556, Japan.
Department of Respiratory Medicine, Graduate School of Medical Sciences, Kumamoto University, Kumamoto-shi, Kumamoto 860-8556, Japan.
Int J Mol Sci. 2020 Dec 19;21(24):9705. doi: 10.3390/ijms21249705.
Evolution of tumor-immune microenviroments (TIMEs) occurs during tumor growth and dissemination. Understanding inter-site tumor-immune heterogeneity is essential to harness the immune system for cancer therapy. While the development of immunotherapy against lung cancer with driver mutations and neuroendocrine tumors is ongoing, little is known about the TIME of large cell neuroendocrine carcinoma (LCNEC) or () rearrangement-positive lung cancer. We present a case study of a 32-year-old female patient with -rearrangement-positive LCNEC, who had multiple distant metastases including mediastinal lymph-node, bilateral breasts, multiple bones, liver and brain. Multiple biopsy samples obtained from primary lung and three metastatic tumors were analyzed by fluorescent multiplex immunohistochemistry. Tissue localizations of tumor-infiltrating lymphocytes in the tumor nest and surrounding stroma were evaluated. T cell and B cell infiltrations were decreased with distance from primary lung lesion. Although each tumor displayed a unique TIME, all tumors exhibited concomitant regression after treatment with an ALK-inhibitor. This study provides the first evidence of the coexistence of distinct TIME within a single individual with -rearrangement-positive LCNEC. The present study contributes to our understanding of heterogeneous TIMEs between primary and metastatic lesions and provides new insights into the complex interplay between host-immunity and cancer cells in primary and metastatic lesions.
肿瘤免疫微环境(TIMEs)在肿瘤生长和扩散过程中发生演变。了解肿瘤免疫异质性对于利用免疫系统进行癌症治疗至关重要。虽然针对具有驱动突变和神经内分泌肿瘤的肺癌的免疫疗法正在不断发展,但对于大细胞神经内分泌癌(LCNEC)或 ()重排阳性肺癌的 TIMEs 知之甚少。我们报告了一例 32 岁女性 -重排阳性 LCNEC 患者的病例研究,该患者有多发性远处转移,包括纵隔淋巴结、双侧乳房、多处骨骼、肝脏和大脑。对原发肺部和三个转移瘤的多个活检样本进行了荧光多重免疫组织化学分析。评估了肿瘤巢和周围基质中浸润性淋巴细胞的组织定位。T 细胞和 B 细胞浸润随着与原发肺部病变的距离增加而减少。尽管每个肿瘤都显示出独特的 TIMEs,但在使用 ALK 抑制剂治疗后,所有肿瘤均显示出协同消退。这项研究首次提供了在单个 -重排阳性 LCNEC 个体中存在不同 TIMEs 的证据。本研究有助于我们了解原发和转移病变之间异质性 TIMEs,并为宿主免疫和原发和转移病变中癌细胞之间的复杂相互作用提供了新的见解。