Prognostic significance of tumor microenvironment assessed by machine learning algorithm in surgically resected non-small cell lung cancer.

IF 2.5 Q4 ONCOLOGY Cancer reports Pub Date : 2026-10-01 Epub Date: 2023-10-30 DOI:10.1002/cnr2.1926
Yukihiro Terada, Mitsuhiro Isaka, Akira Ono, Takuya Kawata, Masakuni Serizawa, Keita Mori, Koji Muramatsu, Kiyoshi Tone, Hirotsugu Kenmotsu, Keiichi Ohshima, Kenichi Urakami, Takeshi Nagashima, Masatoshi Kusuhara, Yasuto Akiyama, Takashi Sugino, Toshiaki Takahashi, Yasuhisa Ohde
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Abstract

Background: A methodology to assess the immune microenvironment (IME) of non-small cell lung cancer (NSCLC) has not been established, and the prognostic impact of IME factors is not yet clear.

Aims: This study aimed to assess the IME factors and evaluate their prognostic values.

Methods and results: We assessed CD8+ tumor-infiltrating lymphocyte (TIL) density, forkhead box protein P3+ (Foxp3+) TIL density, and programmed death receptor ligand-1 (PD-L1) tumor proportion score (TPS) using a machine-learning algorithm in whole-slide imaging (WSI). We dichotomized patients according to TIL density or TPS and compared their clinical outcomes. Between September 2014 and September 2015, 165 patients with NSCLC were enrolled in the study. We assessed IME factors in the epithelium, stroma, and their combination. An improvement in disease-free survival (DFS) was observed in the high CD8+TIL density group in the epithelium, stroma, and the combination of both. Moreover, the group with high PD-L1 TPS in the epithelium showed better DFS than that with low PD-L1 TPS. In the multivariate analysis, the CD8+TIL density in the combination of epithelium and stroma and PD-L1 TPS in the epithelium were independent prognostic factors (hazard ratio [HR] = 0.43; 95% confidence interval [CI] = 0.26-0.72; p = .001, HR = 0.49; 95% CI = 0.30-0.81; p = .005, respectively).

Conclusion: Our approach demonstrated that the IME factors are related to survival in patients with NSCLC. The quantitative assessment of IME factors enables to discriminate patients with high risk of recurrence, who can be the candidates for adjuvant therapy. Assessing the CD8+TIL density in the combination of epithelium and stroma might be more useful than their individual assessment because it is a simple and time-saving analysis of TILs in WSI.

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机器学习算法评估肿瘤微环境对手术切除的癌症的预后意义。
背景:评估癌症(NSCLC)免疫微环境(IME)的方法尚未建立,IME因素对预后的影响尚不清楚。目的:本研究旨在评估IME因素并评估其预后价值。方法和结果:我们在全玻片成像(WSI)中使用机器学习算法评估CD8+肿瘤浸润淋巴细胞(TIL)密度、叉头盒蛋白P3+(Foxp3+)TIL密度和程序性死亡受体配体-1(PD-L1)肿瘤比例评分(TPS)。我们根据TIL密度或TPS对患者进行了二分,并比较了他们的临床结果。2014年9月至2015年9月,165名非小细胞肺癌患者参与了该研究。我们评估了上皮、基质及其组合中的IME因子。在上皮、间质和两者结合的高CD8+TIL密度组中观察到无病生存率(DFS)的改善。此外,上皮中PD-L1 TPS高的组比PD-L1 TPS低的组显示出更好的DFS。在多变量分析中,上皮和间质组合中的CD8+TIL密度以及上皮中的PD-L1 TPS是独立的预后因素(危险比[HR] = 0.43;95%置信区间 = 0.26-0.72;p = .001,小时 = 0.49;95%CI = 0.30-0.81;p = .005)。结论:我们的方法表明IME因素与NSCLC患者的生存率有关。IME因素的定量评估能够区分复发风险高的患者,他们可以成为辅助治疗的候选者。评估上皮和基质组合中的CD8+TIL密度可能比单独评估更有用,因为这是对WSI中TIL的简单且省时的分析。
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来源期刊
Cancer reports
Cancer reports Medicine-Oncology
CiteScore
2.70
自引率
5.90%
发文量
160
审稿时长
17 weeks
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