Evidence map›Paper›PMID 41588364›Full record

ArticleBMC pulmonary medicine2026

Efficacy, safety, and exploratory biomarker analysis of rechallenge with immune checkpoint inhibitors combined with anlotinib in previously treated advanced non-small cell lung cancer.

Li Liu, Haiyan Yang, Yi Xiong, Chunhua Zhou, Wenjuan Jiang, Xingxiang Pu, Jianfu Heng

Abstract read
In one paragraph

Article in BMC pulmonary medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

7 authors.

Li LiuDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University (Hunan Cancer Hospital), No. 283, Tongzipo Road, Yuelu District, Changsha, Hunan Province, 410013, China.
Haiyan YangDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University (Hunan Cancer Hospital), No. 283, Tongzipo Road, Yuelu District, Changsha, Hunan Province, 410013, China.
Yi XiongDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University (Hunan Cancer Hospital), No. 283, Tongzipo Road, Yuelu District, Changsha, Hunan Province, 410013, China.
Chunhua ZhouDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University (Hunan Cancer Hospital), No. 283, Tongzipo Road, Yuelu District, Changsha, Hunan Province, 410013, China.
Wenjuan JiangDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University (Hunan Cancer Hospital), No. 283, Tongzipo Road, Yuelu District, Changsha, Hunan Province, 410013, China.
Xingxiang PuDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University (Hunan Cancer Hospital), No. 283, Tongzipo Road, Yuelu District, Changsha, Hunan Province, 410013, China. Xingxiang92025@126.com.
Jianfu HengDepartment of Medical Oncology, Lung Cancer and Gastrointestinal Unit, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University (Hunan Cancer Hospital), No. 283, Tongzipo Road, Yuelu District, Changsha, Hunan Province, 410013, China. hengjianfu@hnca.org.cn.

Funding

High-Level Talent Support Program of Hunan Cancer Hospital 20250806-1003the science and technology innovation Program of Hunan Province 2021SK51101
6 · The paper itself

Abstract

backgroundImmunotherapy is the standard treatment for driver-negative advanced non-small cell lung cancer (NSCLC), but resistance remains common. Combining anti-angiogenic agents with immune checkpoint inhibitors (ICIs) may reverse resistance. This study evaluated the efficacy, safety, and optimal biomarkers of rechallenge with ICIs combined with anlotinib in advanced NSCLC patients previously treated with ICIs.

methodsA total of 110 advanced NSCLC patients who progressed after prior ICI therapy were rechallenged with ICIs in combination with anlotinib. Primary endpoints included progression-free survival (PFS), overall survival (OS), objective response rate (ORR), and duration of response (DOR). Proteomics was performed on a subset of patients pre- and post-treatment to identify differentially expressed proteins. Patients were categorized into Responder (PFS ≥ 6 months) and Non-responder (PFS < 3 months) groups for proteomic comparison and functional validation of candidate proteins.

resultsPartial response (PR), stable disease (SD), and progressive disease (PD) were achieved in 20.9%, 57.3%, and 20.9% patients. ORR was 20.9% and disease control rate (DCR) was 78.2%, with median DOR of 7 months. Median PFS was 6.0 months and median OS was 16.0 months after rechallenge. Proteomic analysis revealed 91 significantly altered proteins post-treatment. ORM2 and SERPINA1 were hub proteins in the interaction network. External validation suggested a trend toward prolonged survival with high ORM2 and SERPINA1 expression.

conclusionRechallenge with ICIs plus anlotinib demonstrated encouraging efficacy and safety in pretreated advanced NSCLC. Additionally, ORM2 and SERPINA1 were associated with response and survival outcomes in patients treated with the combined ICI + anlotinib regimen and may represent candidate biomarkers of clinical benefit, warranting prospective validation.

Indexed as

Carcinoma, Non-Small-Cell LungImmune Checkpoint InhibitorsIndolesLung NeoplasmsQuinolinesAdultAgedAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorFemaleHumansMaleMiddle AgedProgression-Free SurvivalProteomicsTreatment OutcomeanlotinibBiomarkers, TumorImmune Checkpoint InhibitorsIndolesQuinolinesAnlotinibBiomarkerImmune checkpoint inhibitorsNon-small cell lung cancerProteomicsRechallenge

Identifiers

PMID41588364
PMCPMC13505062

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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 OpenQuestion graph.