A strong association between TTF-1 expression and ILD in predicting the efficacy of PD-1 inhibitor for non-squamous NSCLC patients

Background Thyroid transcriptional factor-1 (TTF-1) is associated with the development of interstitial lung disease (ILD) and is a mutational target in lung adenocarcinoma with ILD. TTF-1 expression is also associated with the efficacy of pemetrexed-based chemotherapy for non-squamous non-small cell...

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Published inERJ open research p. 628
Main Authors Ito, Masaru, Honda, Takayuki, Onishi, Iichiroh, Endo, Satoshi, Mochizuki, Akifumi, Nishiyama, Naoki, Sakakibara, Rie, Takahashi, Susumu, Kumagai, Takashi, Hata, Koki, Yoshii, Sao, Nakamura, Kentaro, Yamashita, Takaaki, Tsukada, Yoshikazu, Chiaki, Tomoshige, Miyashita, Yoshihiro, Natsume, Ichirou, Saitou, Kazuhito, Miyazaki, Yasunari
Format Journal Article
LanguageEnglish
Published 12.09.2024
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Summary:Background Thyroid transcriptional factor-1 (TTF-1) is associated with the development of interstitial lung disease (ILD) and is a mutational target in lung adenocarcinoma with ILD. TTF-1 expression is also associated with the efficacy of pemetrexed-based chemotherapy for non-squamous non-small cell lung cancer (NS-NSCLC). However, the relationship between TTF-1 expression and the efficacy of immunotherapy using programmed cell death 1 inhibitor (PD-1i), especially in lung cancer patients with ILD, remains unclear. Methods Medical data of NS-NSCLC patients treated with PD-1i at multiple centres were analysed retrospectively. Patients were divided into those with or without concomitant ILD, with the two cohorts further stratified by TTF-1 expression. Results The study population included 62 NS-NSCLC patients, 34 with and 28 without ILD. Median progression-free survival (PFS) during PD-1i treatment was significantly shorter in TTF-1-negative than -positive patients (2.0 versus 12.1 months, p=0.004) in the ILD cohort but did not differ significantly in the non-ILD cohort (1.8 versus 2.6 months, p=0.63). Median overall survival (OS) was also significantly shorter in TTF-1-negative than -positive patients in the ILD cohort (14.5 versus 42.5 months, p=0.018) but not in the non-ILD cohort (33.7 versus 37.1 months, p=0.53). Cox regression analyses showed that absence of TTF-1 expression was an independent risk factor for PFS (hazard ratio [HR] 2.75, p=0.024) and OS (HR 2.81, p=0.012) in the ILD cohort. Conclusion TTF-1 expression in NS-NSCLC patients with ILD may predict prognosis when treated with PD-1i.
ISSN:2312-0541
2312-0541
DOI:10.1183/23120541.00628-2024