Evidence map›Paper›PMID 41524997›Full record

ReviewInternational journal of clinical oncology2026

Current development and challenges of NK cell-based immunotherapy for gastrointestinal cancers.

Situo Zheng, Yosuke Morodomi, Yoshikazu Yonemitsu

Abstract readReview
PubMed Publisher
In one paragraph

Review in International journal of clinical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Situo ZhengR&D Laboratory for Innovative Biotherapeutics, Graduate School of Pharmaceutical Science, Kyushu University, Fukuoka, 812-8582, Japan.
Yosuke MorodomiR&D Laboratory for Innovative Biotherapeutics, Graduate School of Pharmaceutical Science, Kyushu University, Fukuoka, 812-8582, Japan. morodomi.yosuke.990@m.kyushu-u.ac.jp.ORCID http://orcid.org/0000-0002-8882-0833
Yoshikazu YonemitsuR&D Laboratory for Innovative Biotherapeutics, Graduate School of Pharmaceutical Science, Kyushu University, Fukuoka, 812-8582, Japan.

Funding

Japan Agency for Medical Research and Development 24014825Japan Agency for Medical Research and Development 24019448Japan Society for the Promotion of Science 23K17433Japan Society for the Promotion of Science 23K27460Japan Society for the Promotion of Science 24H00643Japan Society for the Promotion of Science MJSP2136
6 · The paper itself

Abstract

Despite multimodal treatment options, most gastrointestinal (GI) cancers remain associated with high mortality rates and poor responsiveness to immunotherapy. The remarkable success of immune cell-based therapies in hematologic malignancies has raised interest in translating adoptive cell therapies to GI cancers. Among these approaches, natural killer (NK) cell-based therapies offer potent cytotoxicity, and a favorable safety profile. Multiple NK cell platforms are now under preclinical and clinical development, demonstrating encouraging therapeutic efficacy in GI malignancies. Nevertheless, challenges such as limited in vivo persistence, immunosuppressive tumor microenvironment (TME), and heterogeneous expression of NK cell therapy targeted antigens continue to limit therapeutic benefit. Recent advances are being explored to overcome these barriers and enhance NK cell persistence and specificity. This review summarizes recent progress in NK cell-based immunotherapy for GI cancers, highlights representative clinical trials, and discusses strategies to improve efficacy and durability. With continued innovation, NK cell-based therapy holds promise to become an essential component of the future immunotherapy landscape for GI malignancies.

Indexed as

Adoptive cell transferCancer immunotherapyCAR-NK cellsGastrointestinal cancersNatural killer cellsNK cell therapy

Identifiers

What OpenQuestion holds

Textmetadata
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.