Evidence map›Paper›PMID 35003900›Full record

ArticleOncoimmunology2022

Immunomodulation via FGFR inhibition augments FGFR1 targeting T-cell based antitumor immunotherapy for head and neck squamous cell carcinoma.

Michihisa Kono, Hiroki Komatsuda, Hidekiyo Yamaki, Takumi Kumai, Ryusuke Hayashi, Risa Wakisaka, Toshihiro Nagato, Takayuki Ohkuri, Akemi Kosaka, Kenzo Ohara and 6 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 32 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

16 authors at 1 institution in 1 country.

Michihisa KonoDepartment of Otolaryngology-Head & Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Hiroki KomatsudaDepartment of Otolaryngology-Head & Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Hidekiyo YamakiDepartment of Otolaryngology-Head & Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Takumi KumaiDepartment of Otolaryngology-Head & Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.ORCID 0000-0002-3411-671X
Ryusuke HayashiDepartment of Otolaryngology-Head & Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Risa WakisakaDepartment of Otolaryngology-Head & Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Toshihiro NagatoDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.ORCID 0000-0001-8326-8296
Takayuki OhkuriDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Akemi KosakaDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Kenzo OharaDepartment of Otolaryngology-Head & Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Kan KishibeDepartment of Otolaryngology-Head & Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Miki TakaharaDepartment of Otolaryngology-Head & Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Akihiro KatadaDepartment of Otolaryngology-Head & Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Tatsuya HayashiDepartment of Otolaryngology-Head & Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Hiroya KobayashiDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.
Yasuaki HarabuchiDepartment of Otolaryngology-Head & Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Asahikawa Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibroblast growth factor receptor 1 (FGFR1) is overexpressed in multiple types of solid tumors, including head and neck squamous cell carcinoma (HNSCC). Being associated with poor prognosis, FGFR1 is a potential therapeutic target for aggressive tumors. T cell-based cancer immunotherapy has played a central role in novel cancer treatments. However, the potential of antitumor immunotherapy targeting FGFR1 has not been investigated. Here, we showed that FGFR-tyrosine kinase inhibitors (TKIs) augmented antitumor effects of immune checkpoint inhibitors in an HNSCC mouse model and upregulated tumoral MHC class I and MHC class II expression

Indexed as

Carcinoma, Squamous CellHead and Neck NeoplasmsAnimalsCell Line, TumorHumansImmunotherapyMiceReceptor, Fibroblast Growth Factor, Type 1Squamous Cell Carcinoma of Head and NeckT-LymphocytesFGFR1 protein, humanReceptor, Fibroblast Growth Factor, Type 1FGFR1FGFR tyrosine kinase inhibitorhead and neck squamous cell carcinomaimmunotherapypeptide vaccinetumor-associated antigen

Identifiers

PMID35003900
PMCPMC8741288
OpenAlexW4206494501

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.