Evidence map›Paper›PMID 40799725›Full record

ArticleCancer management and research2025

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

Jun Yamada, Naoe Jimbo, Nanami Yamasaki, Yukihisa Hatakeyama, Tatsunori Kiriu, Natsuhiko Iwamoto, Kanoko Matsumura, Masahiro Katsurada, Keiko Okuno, Kyosuke Nakata and 1 more

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Article in Cancer management and research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Jun YamadaDivision of Respiratory Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.ORCID 0000-0002-7595-5843
Naoe JimboDepartment of Diagnostic Pathology, Kobe University Hospital, Kobe, Japan.
Nanami Yamasaki *Department of Respiratory Medicine, Akashi Medical Center, Akashi, Japan.
Yukihisa Hatakeyama *Department of Respiratory Medicine, Akashi Medical Center, Akashi, Japan.
Tatsunori Kiriu *Department of Respiratory Medicine, Hyogo Prefectural Awaji Medical Center, Sumoto, Japan.ORCID 0000-0001-6877-2005
Natsuhiko Iwamoto *Department of Respiratory Medicine, Takatsuki General Hospital, Takatsuki, Japan.
Kanoko Matsumura *Department of Respiratory Medicine, Takatsuki General Hospital, Takatsuki, Japan.
Masahiro Katsurada *Department of Respiratory Medicine, Hyogo Prefectural Tamba Medical Center, Tamba, Japan.ORCID 0000-0003-4655-3367
Keiko Okuno *Department of Respiratory Medicine, Hyogo Prefectural Tamba Medical Center, Tamba, Japan.
Kyosuke Nakata *Department of Respiratory Medicine, Konan Medical Center, Kobe, Japan.ORCID 0000-0001-8096-865X
Motoko TachiharaDivision of Respiratory Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.ORCID 0000-0002-4598-220X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

advanced lung adenocarcinomaimmunochemotherapyimmunohistochemical stainingTTF-1

Identifiers

PMID40799725
PMCPMC12339237

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