血淋巴细胞作为同期化疗的 III 期非小细胞肺癌的预后因素

Chonnam medical journal Pub Date : 2024-01-01 Epub Date: 2024-01-25 DOI:10.4068/cmj.2024.60.1.40
Yong-Hyub Kim, Yoo-Duk Choi, Sung-Ja Ahn, Young-Chul Kim, In-Jae Oh, Taek-Keun Nam, Jae-Uk Jeong, Ju-Young Song
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引用次数: 0

摘要

我们旨在确定血液淋巴细胞是影响接受同期化疗放疗(CCRT)的局部晚期 III 期非小细胞肺癌(NSCLC)患者生存期的预后因素。本研究对韩国放射肿瘤学组 0903 III 期临床试验的 196 例患者进行了二次研究,以评估循环血淋巴细胞水平的预后意义。CCRT期间总淋巴细胞计数(TLC)减少率的中位数为0.74(范围:0.29-0.97)。在多变量分析中,患者年龄(p=0.014)和肿瘤总体积(GTV,p=0.031)是与总生存期相关的重要因素,而总淋巴细胞减少率(p=0.018)和治疗前中性粒细胞与淋巴细胞比率(NLR,p=0.010)与无进展生存期(PFS)相关。在多变量逻辑回归分析中,治疗前的 NLR、GTV 和心脏 V20 与 TLC 减少显著相关。对84名患者的T细胞上的程序性死亡配体1和CD8表达进行了免疫组化分析。CD8 表达与治疗前淋巴细胞计数无明显相关性(P=0.673),PDL1 表达与 OS 或 PFS 无明显相关性。单变量分析显示,TIL 中 CD8 高表达与良好的 OS 相关,与良好的 PFS 显著相关(p=0.032)。CCRT期间TLC减少是PFS的重要预后因素,而心脏V20与TLC减少显著相关。因此,在免疫疗法时代,为了获得更好的生存结果,必须优先考虑限制整个心脏的放射剂量体积。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Blood Lymphocytes as a Prognostic Factor for Stage III Non-Small Cell Lung Cancer with Concurrent Chemoradiation.

We aimed to identify blood lymphocytes as a prognostic factor for survival in patients with locally advanced stage III non-small cell lung cancer (NSCLC) treated with concurrent chemoradiotherapy (CCRT). This is a secondary study of 196 patients enrolled in the Korean Radiation Oncology Group 0903 phase III clinical trial to evaluate the prognostic significance of circulating blood lymphocyte levels. The median total lymphocyte count (TLC) reduction ratio during CCRT was 0.74 (range: 0.29-0.97). In multivariate analysis, patient age (p=0.014) and gross tumor volume (GTV, p=0.031) were significant factors associated with overall survival, while TLC reduction (p=0.018) and pretreatment neutrophil-to-lymphocyte ratio (NLR; p=0.010) were associated with progression-free survival (PFS). In multivariate logistic regression analysis, pretreatment NLR, GTV, and heart V20 were significantly associated with TLC reduction. Immunohistochemical analysis of programmed death ligand 1 and CD8 expression on T cells was performed on 84 patients. CD8 expression was not significantly associated with the pretreatment lymphocyte count (p=0.673), and PDL1 expression was not significantly associated with OS or PFS. Univariate analysis revealed that high CD8 expression in TILs was associated with favorable OS and was significantly associated with favorable PFS (p=0.032). TLC reduction during CCRT is a significant prognostic factor for PFS, and heart V20 is significantly associated with TLC reduction. Thus, in the era of immunotherapy, constraining the volume of the radiation dose to the whole heart must be prioritized for the better survival outcomes.

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