Evidence map›Paper›PMID 41415283›Full record

Observational studyFrontiers in immunology2025

Combination immunotherapy and anti-angiogenic therapy shows promising efficacy in NSCLC patients with recurrent or refractory brain metastases and negative driver genes.

Liwei Sun, Bonian Chen, Bin Wang, Jinduo Li, Lin Li, Caijuan Tian, Hongbo Zhang, Pengfei Liu, Xiaomin Liu

Abstract readObservational Study
In one paragraph

Observational study in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
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

9 authors.

Liwei Sun *Department of Oncology, Tianjin Huanhu Hospital, Tianjin Key Laboratory of Cerebral Vascular and Neurodegenerative Disease, Tianjin Neurosurgical Institute, Tianjin, China.
Bonian Chen *Department of Medical Insurance, Tianjin Huanhu Hospital, Tianjin Key Laboratory of Cerebral Vascular and Neurodegenerative Disease, Tianjin Neurosurgical Institute, Tianjin, China.
Bin WangDepartment of Oncology, Tianjin Huanhu Hospital, Tianjin Key Laboratory of Cerebral Vascular and Neurodegenerative Disease, Tianjin Neurosurgical Institute, Tianjin, China.
Jinduo LiDepartment of Oncology, Tianjin Huanhu Hospital, Tianjin Key Laboratory of Cerebral Vascular and Neurodegenerative Disease, Tianjin Neurosurgical Institute, Tianjin, China.
Lin LiDepartment of Oncology, Tianjin Huanhu Hospital, Tianjin Key Laboratory of Cerebral Vascular and Neurodegenerative Disease, Tianjin Neurosurgical Institute, Tianjin, China.
Caijuan TianTianjin Marvel Medical Laboratory, Tianjin Marvelbio Technology Co., Ltd, Tianjin, China.
Hongbo ZhangTianjin Marvel Medical Laboratory, Tianjin Marvelbio Technology Co., Ltd, Tianjin, China.
Pengfei LiuDepartment of Oncology, Institute of Basic Research, Tianjin Academy of Traditional Chinese Medicine, Tianjin Academy of Traditional Chinese Medicine Affiliated Hospital, Tianjin, China.
Xiaomin LiuDepartment of Oncology, Tianjin Huanhu Hospital, Tianjin Key Laboratory of Cerebral Vascular and Neurodegenerative Disease, Tianjin Neurosurgical Institute, Tianjin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: This study aimed to evaluate the efficacy of immunotherapy combined with anti-angiogenic therapy for non-small cell lung cancer (NSCLC) with brain metastasis (BM) and negative driver genes. Methods: This observational prospective study was conducted using the clinical data of 34 patients with NSCLC and BM, including 24 patients who received immunotherapy combined with anti-angiogenic therapy and 10 control patients using oral anlotinib upon the first- to fourth-line treatment failure or refusing to continue chemotherapy between June 2017 and August 2022. Efficacy was evaluated using progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), and adverse reactions. Results: Among 24 patients treated with immunotherapy combined with anti-angiogenic therapy, 17 had a partial response, six had stable disease, and one had progressive disease. The ORR and DCR of patients receiving immunotherapy combined with anti-angiogenic therapy were 70.8% and 95.8%, respectively. The median PFS of immunotherapy combined with anti-angiogenic treatment was significantly longer than that of oral anlotinib (18.0 Conclusion: Immunotherapy combined with anti-angiogenic therapy in patients with recurrent or refractory NSCLC and BM driven by negative genes has yielded promising but preliminary findings. Clinical Trial Registration: www.chictr.org.cn, identifier ChiCTR1800017499.

Indexed as

Angiogenesis InhibitorsBrain NeoplasmsCarcinoma, Non-Small-Cell LungImmunotherapyLung NeoplasmsAdultAgedAntineoplastic Combined Chemotherapy ProtocolsFemaleHumansIndolesMaleMiddle AgedNeoplasm Recurrence, LocalProspective StudiesQuinolinesAngiogenesis InhibitorsanlotinibIndolesQuinolinesanti-angiogenic therapybrain metastasisimmunotherapynon-small cell lung cancerprospective observational study

Identifiers

PMID41415283
PMCPMC12708319

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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.