免疫检查点阻断通过扩增效应 CD8⁺ T 细胞克隆增强淋巴细胞清除性化疗诱导的抗肿瘤免疫
Immune Checkpoint Blockade Augments Lymphodepleting Chemotherapy-Induced Antitumor Immunity by Expanding Effector CD8+ T-cell Clones.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A Retrospective, Observational Analysis of Tumor Infiltrating Lymphocytes and Tumor Regression in Melanoma.
A Retrospective, Observational Analysis of Tumor Infiltrating Lymphocytes and Tumor Regression in Melanoma.
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与不活跃或缺失的 TILs 相比,活跃的 TILs 与较薄的肿瘤及存在肿瘤消退呈正相关。
TIL(肿瘤浸润淋巴细胞)和肿瘤消退被认为是黑色素瘤免疫反应的不同标志。
分析 TIL 分级与消退表现彼此之间,以及与其他预后组织病理学和临床指标之间的关系。
回顾性分析 2013 至 2019 年确诊且有完整组织病理报告的黑色素瘤患者。
TIL 显著、TIL 不显著和无 TIL 患者中,分别有 48.9%、30.1% 和 37.9% 出现肿瘤消退(P=0.019)。与 TIL 不显著或无 TIL 的肿瘤相比,TIL 显著的黑色素瘤 Breslow 厚度较低(P=0.001)。有肿瘤消退的肿瘤 Breslow 厚度也较低(P<0.001)。TIL 分级和肿瘤消退均不能预防淋巴结转移,也与生存改善无关。
与 TIL 不显著或无 TIL 相比,TIL 显著与肿瘤厚度较薄及存在肿瘤消退呈正相关,提示 TIL 显著的肿瘤可能具有更强的免疫反应。进一步探究 TIL 分级、淋巴细胞亚型和淋巴细胞密度之间的关系,或有助于解释这一发现。
Tumor infiltrating lymphocytes (TILs) and regression are thought to be distinct markers of the immune response to melanoma.
This study sought to analyze the relationship of TIL grade and presence of regression to each other and to other prognostic histopathologic and clinical values in melanoma.
A retrospective analysis was conducted using patients diagnosed with melanoma between 2013 and 2019 whose complete histopathologic reports were available.
Regression was seen in 48.9%, 30.1% and 37.9% of patients with brisk, non-brisk, and absent TILs respectively (P=0.019). Melanoma tumors with brisk TILs were found to have a lower Breslow thickness than those with non-brisk or absent (P= 0.001). Tumors with regression were also found to have lower Breslow thickness (P<0.001). Neither TIL grade nor regression were protective of nodal metastasis or associated with improved survival.
Brisk TILs have a positive association with thinner tumors and the presence of tumor regression relative to non-brisk or absent TILs. This may suggest a more robust immune response in tumors with brisk TILs. Further exploration of the interplay between TIL grade, lymphocyte cell subtype and lymphocyte density may help explain this finding.
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