Nishioka Naoya, Hata Tae, Yamada Tadaaki, Goto Yasuhiro, Amano Akihiko, Negi Yoshiki, Watanabe Satoshi, Furuya Naoki, Oba Tomohiro, Ikoma Tatsuki, Nakao Akira, Tanimura Keiko, Taniguchi Hirokazu, Yoshimura Akihiro, Fukui Tomoya, Murata Daiki, Kaira Kyoichi, Shiotsu Shinsuke, Hibino Makoto, Okada Asuka, Chihara Yusuke, Kawachi Hayato, Kijima Takashi, Takayama Koichi
Department of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Department of Respiratory Medicine, Fujita Health University School of Medicine, Aichi, Japan.
Cancer Res Treat. 2025 Apr;57(2):412-421. doi: 10.4143/crt.2024.748. Epub 2024 Oct 25.
Thyroid transcription factor 1 (TTF-1) expression is a useful predictor of treatment efficacy in advanced non-squamous non-small cell lung cancer (NSCLC). This study aimed to evaluate whether TTF-1 could predict the effectiveness of chemotherapy versus chemoimmunotherapy in patients with non-squamous NSCLC with programmed death ligand-1 (PD-L1) expression between 1% and 49%.
We conducted a retrospective study of patients with NSCLC who were treated with chemotherapy or chemoimmunotherapy between March 2016 and May 2023. The patients had histologically confirmed NSCLC, stage III-IV or postoperative recurrence, TTF-1 measurements, and PD-L1 expression levels between 1% and 49%. Clinical data were analyzed to evaluate the effect of TTF-1 expression on treatment efficacy.
This study included 283 of 624 patients. TTF-1-positive patients showed longer progression-free survival (PFS) and overall survival (OS) (PFS: 6.4 months [95% confidence interval (CI), 5.0 to 9.4] vs. 4.1 months [95% CI, 2.7 to 6.1], p=0.03; OS: 17.9 months [95% CI, 15.2 to 28.1] vs. 9.4 months [95% CI, 6.3 to 17.0], p < 0.01) in the chemotherapy cohorts (n=93). In the chemoimmunotherapy cohort (n=190), there was no significant difference in PFS and OS between TTF-1-positive and -negative groups (PFS: 7.6 months [95% CI, 6.4 to 11.0] vs. 6.0 months [95% CI, 3.6 to 12.6], p=0.59; OS: 25.0 months [95% CI, 18.0 to 49.2] vs. 21.3 months [95% CI, 9.8 to 28.8], p=0.09).
In patients with NSCLC with PD-L1 expression between 1% and 49%, TTF-1 expression was a predictor of chemotherapeutic, but not chemoimmunotherapeutic, efficacy.
甲状腺转录因子1(TTF-1)表达是晚期非鳞状非小细胞肺癌(NSCLC)治疗疗效的有用预测指标。本研究旨在评估TTF-1是否能预测程序性死亡配体1(PD-L1)表达为1%至49%的非鳞状NSCLC患者化疗与化疗免疫治疗的疗效。
我们对2016年3月至2023年5月期间接受化疗或化疗免疫治疗的NSCLC患者进行了一项回顾性研究。这些患者经组织学确诊为NSCLC,处于III-IV期或术后复发,有TTF-1测量值,且PD-L1表达水平在1%至49%之间。分析临床数据以评估TTF-1表达对治疗疗效的影响。
本研究纳入了624例患者中的283例。在化疗队列(n=93)中,TTF-1阳性患者的无进展生存期(PFS)和总生存期(OS)更长(PFS:6.4个月[95%置信区间(CI),5.0至9.4]对4.1个月[95%CI,2.7至6.1],p=0.03;OS:17.9个月[95%CI,15.2至28.1]对9.4个月[95%CI,6.3至17.0],p<0.01)。在化疗免疫治疗队列(n=190)中,TTF-1阳性和阴性组之间的PFS和OS无显著差异(PFS:7.6个月[95%CI,6.4至11.0]对6.0个月[95%CI,3.6至12.6],p=0.59;OS:25.0个月[95%CI,18.0至49.2]对21.3个月[95%CI,9.8至28.8],p=0.09)。
在PD-L1表达为1%至49%的NSCLC患者中,TTF-1表达是化疗疗效的预测指标,但不是化疗免疫治疗疗效的预测指标。