Evidence map›Paper›PMID 35356198›Full record

ArticleFrontiers in oncology2022

Incorporation of SKI-G-801, a Novel AXL Inhibitor, With Anti-PD-1 Plus Chemotherapy Improves Anti-Tumor Activity and Survival by Enhancing T Cell Immunity.

Wongeun Lee, Dong Kwon Kim, Chun-Bong Synn, Hee Kyu Lee, Sungho Park, Dong-Sik Jung, Yewon Choi, Jae Hwan Kim, Youngseon Byeon, Young Seob Kim and 18 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

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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

28 authors at 4 institutions in 1 country.

Wongeun LeeJEUK Institute for Cancer Research, JEUK Co., Ltd., Gumi-si, South Korea.
Dong Kwon KimSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
Chun-Bong SynnSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
Hee Kyu LeeDepartment of Discovery Biology, Oscotec Inc., Seongnam, South Korea.
Sungho ParkDepartment of Discovery Biology, Oscotec Inc., Seongnam, South Korea.
Dong-Sik JungDepartment of Discovery Biology, Oscotec Inc., Seongnam, South Korea.
Yewon ChoiDepartment of Discovery Biology, Oscotec Inc., Seongnam, South Korea.
Jae Hwan KimSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
Youngseon ByeonSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
Young Seob KimSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
Seul LeeSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
Soyeon LeeSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
Yunjoo JooSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
Eun Ji LeeSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
Mi Ran YunJEUK Institute for Cancer Research, JEUK Co., Ltd., Gumi-si, South Korea.
Seong Gu HeoSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
Wookyeom YangSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
Ji Eun JungSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
Eun Kyung KimSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
Jooyeon ParkSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
June Dong ParkWide River Institute of Immunology, Seoul National University, Hongcheon, South Korea.
Doo Jae LeeWide River Institute of Immunology, Seoul National University, Hongcheon, South Korea.
Hyeon-Woo KimWide River Institute of Immunology, Seoul National University, Hongcheon, South Korea.
Sun Min LimDivision of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea.
Min Hee HongDivision of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea.
Beung-Chul AhnDivision of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea.
Jii Bum LeeDivision of Hemato-oncology, Wonju Severance Christian Hospital, Yonsei University Wonju College of Medicine, Wonju, South Korea.
Kyoung-Ho PyoSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea.
Yonsei University · KRSeoul National University · KRJeuk (South Korea) · KRNational Cancer Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A recently developed treatment strategy for lung cancer that combines immune checkpoint inhibitors with chemotherapy has been applied as a standard treatment for lung adenocarcinoma (LUAD) and lung squamous cell carcinoma (LUSC), and it has improved the outcomes of chemotherapy. Maintenance treatment with anti-PD-1 antibody (aPD-1) enhances the effect of immunochemical combination therapy and improves therapeutic efficacy, which contributes toward a significant improvement in patient survival rates. The AXL receptor tyrosine kinase (AXL), which is expressed in tumor cells, plays an essential role in the resistance of cancers to chemotherapy and immunotherapy, and stimulates signaling associated with epithelial-mesenchymal transition (EMT) in metastatic cancer. AXL is thus an attractive target for controlling resistance to anti-tumor therapies. In this study, we examined the effect of AXL inhibitors on immune activation and tumor growth in TC1 and C3PQ mouse tumor models, in the context of clinical immunotherapy/chemotherapy and maintenance treatment, using an aPD-1 with/without pemetrexed. To determine the optimal timing for administration of SKI-G-801, an AXL inhibitor, we investigated its anti-tumor effects based on inclusion at the immunochemotherapy and maintenance therapy stages. We also performed flow cytometry-based immune profiling of myeloid cells and lymphoid cells at different points in the treatment schedule, to investigate the immune activation and anti-tumor effects of the AXL inhibitor. The addition of SKI-G-801 to the immune checkpoint inhibitor and chemotherapy stage, as well as the maintenance therapy stage, produced the best anti-tumor results, and significant tumor growth inhibition was observed in both the TC1 and C3PQ models. Both models also exhibited increased proportion of effector memory helper T cells and increased expression of CD86

Indexed as

AXL receptor tyrosine kinasechemotherapyepithelial-mesenchymal transitionimmunotherapynon-small cell lung cancer

Identifiers

PMID35356198
PMCPMC8959645
OpenAlexW4220778216

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.