Evidence map›Paper›PMID 36357599›Full record

ArticleCancer immunology, immunotherapy : CII2023

Combined pembrolizumab and bevacizumab therapy effectively inhibits non-small-cell lung cancer growth and prevents postoperative recurrence and metastasis in humanized mouse model.

Tianyun Qiao, Jinbo Zhao, Xiangbing Xin, Yanlu Xiong, Wenwen Guo, Fancheng Meng, Hui Li, Yangbo Feng, Hui Xu, Changhong Shi and 1 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2023. 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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
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  9. Noncanonical functions of adhesion proteins in inflammation.American journal of physiology. Cell physiology · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Tianyun Qiao *Department of Thoracic Surgery, Air Force Specialty Medical Center, Fourth Military Medical University, Xi'an, 710032, China.
Jinbo Zhao *Department of Thoracic Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, 710032, China.
Xiangbing Xin *Department of Thoracic Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, 710032, China.
Yanlu XiongDepartment of Thoracic Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, 710032, China.
Wenwen GuoLaboratory Animal Center, Fourth Military Medical University, Xi'an, 710032, China.
Fancheng MengDepartment of Thoracic Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, 710032, China.
Hui LiLaboratory Animal Center, Fourth Military Medical University, Xi'an, 710032, China.
Yangbo FengDepartment of Thoracic Surgery, Air Force Specialty Medical Center, Fourth Military Medical University, Xi'an, 710032, China.
Hui XuSchool of Basic Medicine, Fourth Military Medical University, Xi'an, 710032, China. xubz@fmmu.edu.cn.
Changhong ShiLaboratory Animal Center, Fourth Military Medical University, Xi'an, 710032, China. changhong@fmmu.edu.cn.
Yong HanDepartment of Thoracic Surgery, Air Force Specialty Medical Center, Fourth Military Medical University, Xi'an, 710032, China. hanyong_td@163.com.
Air Force Medical University · CN

Funding

National Natural Science Foundation of China 81001041
6 · The paper itself

Abstract

Antibodies targeting the programmed cell death protein 1/programmed cell death ligand-1 (PD-1/PD-L1) pathway have dramatically changed the treatment landscape of advanced non-small cell lung cancer (NSCLC). However, combination approaches are required to extend this benefit beyond a subset of patients. In addition, it is of equal interest whether these combination therapy can be applied to neoadjuvant therapy of early-stage NSCLC. In this study, we hypothesized that combining immunotherapy with anti-angiogenic therapy may have a synergistic effect in local tumor control and neoadjuvant therapy. To this end, the effect of combination of bevacizumab and pembrolizumab in humanized mouse models was evaluated. Furthermore, we innovatively constructed a neoadjuvant mouse model that can simulate postoperative recurrence and metastasis of NSCLC to perform neoadjuvant study. Tumor growth and changes in the tumor vasculature, along with the frequency and phenotype of tumor-infiltrating lymphocytes, were examined. Additionally, in vivo imaging system (IVIS) was used to observe the effect of neoadjuvant therapy. Results showed that combination therapy could inhibited tumor growth by transforming tumor with low immunoreactivity into inflamed ('hot') tumor, as demonstrated by increased CD8

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAnimalsAntibodies, Monoclonal, HumanizedB7-H1 AntigenBevacizumabMiceAntibodies, Monoclonal, HumanizedB7-H1 AntigenBevacizumabpembrolizumabAnti-programmed death 1Anti-vascular endothelial growth factorHumanized mouse modelImmunotherapyNeoadjuvant therapyNon-small cell lung cancer

Identifiers

PMID36357599
PMCPMC10110651
OpenAlexW4308767352

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.