Evidence map›Paper›PMID 33457101›Full record

ArticleOncoimmunology2020

Pirfenidone facilitates immune infiltration and enhances the antitumor efficacy of PD-L1 blockade in mice.

Wan Qin, Jun Zou, Yongbiao Huang, Chaofan Liu, Yalin Kang, Hu Han, Yang Tang, Long Li, Bo Liu, Weiheng Zhao and 1 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
6.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 65 citations in OpenAlex.

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  5. Risk factors and management of lung cancer in idiopathic pulmonary fibrosis: A comprehensive review.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Wan QinDepartment of Oncology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Jun ZouDepartment of Oncology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Yongbiao HuangDepartment of Oncology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Chaofan LiuDepartment of Oncology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Yalin KangDepartment of Oncology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Hu HanDepartment of Oncology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Yang TangDepartment of Oncology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Long LiDepartment of Oncology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Bo LiuDepartment of Oncology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Weiheng ZhaoDepartment of Oncology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Xianglin YuanDepartment of Oncology, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Huazhong University of Science and Technology · CNTongji Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) patients have a high risk of developing lung cancer, with few treatment options available. Pirfenidone, an antifibrotic agent approved for the treatment of IPF, has been demonstrated to suppress the TGFβ signaling and modulate the expression of immune-related genes. However, for lung cancer patients with comorbid IPF, whether pirfenidone has any synergetic effect with immune checkpoint inhibitors has not been investigated. In this study, we showed that pirfenidone monotherapy attenuated tumor growth with an increased T cell inflammatory signature in tumors. Co-administration of pirfenidone with PD-L1 blockades significantly delayed the tumor growth and increased survival, compared with the effect of either treatment alone. Combination therapy promoted gene expression with a unique signature associated with innate and adaptive immune response resulted in the infiltration of immune cells and optimal T cell positioning. Furthermore, we showed a great benefit of combination therapy in alleviating the pulmonary fibrosis and reducing the tumor growth in a tumor-fibrosis model. Our results collectively demonstrated that pirfenidone facilitated antitumor immunity and enhanced the efficacy of PD-L1 blockades. It may act as an adjuvant to immunotherapy in cancer treatment, particularly, in lung cancer patients with preexisting IPF.

Indexed as

Idiopathic Pulmonary FibrosisLung NeoplasmsAnimalsB7-H1 AntigenHumansMicePyridonesB7-H1 AntigenpirfenidonePyridonesidiopathic pulmonary fibrosisimmune-checkpoint inhibitorsLung cancerPD-L1 blockadespirfenidone

Identifiers

PMID33457101
PMCPMC7781712
OpenAlexW3088048752

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.