Evidence map›Paper›PMID 41071328›Full record

Observational studyCancer immunology, immunotherapy : CII2025

Bevacizumab reduces PD-L1 Not PD-1 inhibitor-associated pneumonitis in non-small cell lung cancer patients.

Linling Wang, Yasi Xu, Yanyan Zhao, Bing Xia, Lucheng Zhu

Erratum issuedAbstract readObservational Study
In one paragraph

Observational study in Cancer immunology, immunotherapy : CII, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Linling Wang *The Fourth School of Clinical Medicine, Affiliated Zhejiang Chinese Medical University, Zhejiang, People's Republic of China.
Yasi Xu *The Fourth School of Clinical Medicine, Affiliated Zhejiang Chinese Medical University, Zhejiang, People's Republic of China.
Yanyan ZhaoDepartment of Translational Medicine Research Center, Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University, Hangzhou, People's Republic of China.
Bing XiaDepartment of Thoracic Oncology, Affiliated Hangzhou Cancer Hospital, Zhejiang Chinese Medical University, No. 34, Yanguan Lane, Hangzhou, 310002, People's Republic of China.
Lucheng ZhuDepartment of Thoracic Oncology, Affiliated Hangzhou Cancer Hospital, Zhejiang Chinese Medical University, No. 34, Yanguan Lane, Hangzhou, 310002, People's Republic of China. zhulucheng1@zuaa.zju.edu.cn.

Funding

Hangzhou Science and Technology Development Plan Project 202004A19National Natural Science Foundation of China 82373889Youth Science and Technology Innovation Training Project of Hangzhou Cancer Hospital HZCH2021QN01
6 · The paper itself

Abstract

backgroundInterstitial pneumonitis (IP) is a severe adverse event in patients receiving immunotherapy. Although PD-1/PD-L1 inhibitors and bevacizumab have been widely used in patients with non-small cell lung cancer (NSCLC), the interaction between their combination and IP is less known.

methodsTo investigate the interaction between bevacizumab and PD-1/PD-L1 inhibitors on IP, an observational study between January 2012 and June 2023, US, from the Food and Drug Administration Adverse Event Reporting System (FAERS) database including 55,673 NSCLC patients was performed. The reported proportions of PD-1/PD-L1 inhibitor-associated IP in patients receiving and not receiving bevacizumab treatment were compared.

resultsA total of 23,790 and 4753 patients were treated with PD-1/PD-L1 inhibitors and bevacizumab, among whom 1693 were treated with both PD-1/PD-L1 inhibitors and bevacizumab. The proportions of IP were 7.3% (95% CI 7.1 to 7.5%) in the total population of patients with NSCLC, 11.1% in patients treated with PD-1/PD-L1 inhibitors, and 4.4% in patients treated with bevacizumab. The reported IP proportion was 15.4% for PD-1 inhibitors with bevacizumab, which was greater than the 9.1% for PD-1 inhibitors without bevacizumab, while the opposite trend was observed for PD-L1 inhibitors (4.4% for bevacizumab vs 19.6% for PD-L1 inhibitors without bevacizumab).

conclusionsOur study showed that bevacizumab was associated with a higher reported proportion of PD-1 inhibitor-associated IP but a lower reported proportion of PD-L1 inhibitor-associated IP. Although this was a post-marketing, observational study with many limitations, bevacizumab might be a proper combination with PD-L1 inhibitors in consideration of IP, especially in patients at high risk of IP. However, this relationship still needs further clinical validation.

Indexed as

B7-H1 AntigenBevacizumabCarcinoma, Non-Small-Cell LungImmune Checkpoint InhibitorsLung Diseases, InterstitialLung NeoplasmsPneumoniaAgedFemaleHumansMaleMiddle AgedProgrammed Cell Death 1 ReceptorB7-H1 AntigenBevacizumabCD274 protein, humanImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorBevacizumabCheckpoint inhibitorsInterstitial pneumonitisNon-small cell lung cancerProgrammed cell death 1 ligand 1Programmed death 1

Identifiers

PMID41071328
PMCPMC12514101

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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.