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弥漫性和强 TTF-1 表达可预测晚期肺腺癌对培美曲塞为基础的免疫化疗的反应。

Diffuse and Strong TTF-1 Expression Predicts Response to Pemetrexed-Based Immunochemotherapy in Advanced Lung Adenocarcinoma.

作者信息

Yamada Jun, Jimbo Naoe, Yamasaki Nanami, Hatakeyama Yukihisa, Kiriu Tatsunori, Iwamoto Natsuhiko, Matsumura Kanoko, Katsurada Masahiro, Okuno Keiko, Nakata Kyosuke, Tachihara Motoko

机构信息

Division of Respiratory Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.

Department of Diagnostic Pathology, Kobe University Hospital, Kobe, Japan.

出版信息

Cancer Manag Res. 2025 Aug 7;17:1599-1611. doi: 10.2147/CMAR.S520436. eCollection 2025.

Abstract

PURPOSE

Thyroid transcription factor-1 (TTF-1) is a good prognostic factor for non-small cell lung carcinoma (NSCLC). It is unclear how much TTF-1 staining is sufficient to predict therapeutic response in immunochemotherapy. We evaluated the cut-off of TTF-1 considering the percentage of positive cells and staining intensity as a predictive factor.

PATIENTS AND METHODS

We conducted a retrospective multicenter study of patients with advanced lung adenocarcinoma or NSCLC favor adenocarcinoma treated with immunochemotherapy. One pathologist centrally examined the immunohistochemical staining of TTF-1 using 8G7G3/1 and provided scores of 0-5 based on the staining intensity and ratio.

RESULTS

We analyzed 95 patients. As TTF-1 has previously been shown to be a predictive factor for pemetrexed, there were significant differences in PFS of patients treated with pemetrexed-based immunochemotherapy between TTF-1 scores of 5 (diffuse and strong staining) and ≤4, but not between 0 (no staining) and 2-4 (partial or weak staining). We defined a TTF-1 score of ≥5 as positive for the predictive factor and the positivity ratio was 61.1%. Patients who tested negative for TTF-1 had a significantly higher proportion of programmed death ligand 1 (PD-L1) tumor proportion score (TPS) <1%. Excluding mutation-positive patients, PFS in TTF-1 positivity was significantly longer than in negativity (8.0 and 5.9, hazard ratio (HR): 0.58 (0.34-0.98), p = 0.04), while TTF-1 negativity was not inferior to positivity in PFS with taxane-based immunochemotherapy. Patients treated with pemetrexed-based immunochemotherapy who tested positive for TTF-1 had significantly longer PFS than those who tested negative (HR: 0.51 (0.27-0.99), p = 0.045) in the multivariate analysis incorporating age, PD-L1, PS, and TTF-1.

CONCLUSION

Diffuse and strong TTF-1 positivity may be useful for the predictive factor for pemetrexed-based immunochemotherapy. TTF-1 staining may be desirable to develop a more optimal immunochemotherapy for lung adenocarcinoma.

摘要

目的

甲状腺转录因子-1(TTF-1)是非小细胞肺癌(NSCLC)的一个良好预后因素。目前尚不清楚TTF-1染色强度达到多少足以预测免疫化疗的治疗反应。我们将阳性细胞百分比和染色强度作为预测因素,评估了TTF-1的临界值。

患者与方法

我们对接受免疫化疗的晚期肺腺癌或倾向于腺癌的NSCLC患者进行了一项回顾性多中心研究。一名病理学家使用8G7G3/1对TTF-1进行集中免疫组化染色检查,并根据染色强度和比例给出0-5分的评分。

结果

我们分析了95例患者。由于TTF-1先前已被证明是培美曲塞的预测因素,在接受以培美曲塞为基础的免疫化疗的患者中,TTF-1评分为5分(弥漫性强染色)和≤4分的患者的无进展生存期(PFS)存在显著差异,但评分为0分(无染色)和2-4分(部分或弱染色)的患者之间无显著差异。我们将TTF-1评分为≥5分定义为预测因素阳性,阳性率为61.1%。TTF-1检测为阴性的患者中,程序性死亡配体1(PD-L1)肿瘤比例评分(TPS)<1%的比例显著更高。排除突变阳性患者后,TTF-1阳性患者的PFS显著长于阴性患者(8.0和5.9,风险比(HR):0.58(0.34-0.98),p = 0.04),而在接受以紫杉烷为基础的免疫化疗时,TTF-1阴性患者的PFS并不逊于阳性患者。在纳入年龄、PD-L1、PS和TTF-1的多因素分析中,接受以培美曲塞为基础的免疫化疗且TTF-1检测为阳性的患者的PFS显著长于检测为阴性的患者(HR:0.51(0.27-0.99),p =

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