癌症瘤内和瘤周淋巴细胞反应与生存率的相关性

C. Su, Tzu-Yin Tang, Chi-Jung Li, Yu‐Chuen Huang, Yu-Jen Chen
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摘要

背景:具有高水平微卫星不稳定性(MSI-H)的癌症(CRC)与生存率的提高有关。肿瘤微环境(TME)中淋巴细胞显著浸润的组织病理学评估,包括肿瘤内淋巴细胞反应(ILR)和肿瘤周围淋巴细胞反应(PLR),用于预测MSI-H。然而,由于主要的新辅助同期放化疗(CCRT)治疗,淋巴细胞反应预测癌症生存率的直接病理学证据缺乏。本研究旨在确定PLR和ILR的表型是否与局部晚期癌症接受明确手术后辅助CCRT的临床结果相关。方法:从2005年到2018年,在麦凯纪念医院登记的121名患者中,55份样本可评估淋巴细胞反应。ILR和PLR根据美国病理学家学会(CAP)发布的癌症报告方案进行评估。根据阳性或阴性ILR/PLR,我们将每位患者分为四组之一:ILR+/PLR+、ILR+/PLL-、ILR-/PLR+或ILR-/PLR−。结果:与ILR或PLR的阳性淋巴细胞反应相比,ILR−/PLR−与较差的总生存率显著相关。多因素分析显示,在根据临床特征进行调整后,ILR−/PLR−是总生存率的一个重要风险因素。结论:肿瘤微环境(TME)中的淋巴细胞反应可以预测不良生存结果,也是免疫治疗的潜在指标。
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Intratumoral and peritumoral lymphocytic responses correlate with survival in rectal cancer
Background: Colorectal cancer (CRC) with high level of microsatellite instability (MSI-H) is associated with improved survival. Histopathological assessment of prominent infiltration of lymphocytes in tumor microenvironment (TME), including intratumoral lymphocytic response (ILR) and peritumoral lymphocytic response (PLR), was utilized to predict MSI-H. However, the direct pathological evidence of lymphocytic response predicting survival of rectal cancer is lacking due to the predominant neoadjuvant concurrent chemoradiotherapy (CCRT) treatment. This study aims to identify whether the phenotype of PLR and ILR is associated with the clinical outcome of locally-advanced rectal cancer receiving definitive surgery followed by adjuvant CCRT. Methods: From 2005 to 2018, among the 121 patients enrolled from MacKay Memorial Hospital, 55 specimen was assessable for lymphocytic response. ILR and PLR were assessed according to the cancer reporting protocol released by the College of American Pathologists (CAP). Based on positive or negative ILR/PLR, we categorized each patient as one of the four groups: ILR+/PLR+, ILR+/PLR−, ILR−/PLR+, or ILR−/PLR−. Results: ILR−/PLR− was significantly associated with poorer overall survival, compared to either positive lymphocytic response of ILR or PLR. Multivariate analysis revealed ILR−/PLR− as a significant risk factor for overall survival after adjusting with clinical characteristics. Conclusions: Lymphocytic response in tumor microenvironment (TME) can be a predictor for poor survival outcome and a potential indicator for immunotherapy.
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