Evidence map›Paper›PMID 42702375›Full record

ReviewZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences2026

[Current status and challenges of artificial intelligence and organoid technologies in precision diagnosis and treatment of gastrointestinal stromal tumors].

Junzhao You, Hongtao Tang, Shun Jiang, Zhengchao Quan, Yimou Zhang, Nengyi Hou, Chuan Zhou, Minghui Pang

Abstract readReviewEnglish Abstract
In one paragraph

Review in Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences, 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

8 authors.

Junzhao YouSchool of Medicine, University of Electronic Science and Technology of China, Chengdu 610054. 18161275069@163.com.
Hongtao TangSchool of Clinical Medicine, North Sichuan Medical College, Nanchong 637100.
Shun JiangDepartment of Gastrointestinal Surgery, Affiliated Hospital of Southwest Medical University, Luzhou 646000.
Zhengchao QuanSchool of Medicine, University of Electronic Science and Technology of China, Chengdu 610054.
Yimou ZhangSchool of Clinical Medicine, North Sichuan Medical College, Nanchong 637100.
Nengyi HouSchool of Medicine, University of Electronic Science and Technology of China, Chengdu 610054.
Chuan ZhouSchool of Medicine, University of Electronic Science and Technology of China, Chengdu 610054.
Minghui PangSchool of Medicine, University of Electronic Science and Technology of China, Chengdu 610054. mhpang@uestc.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastrointestinal stromal tumor (GIST) is the most common mesenchymal tumor of the gastrointestinal tract. Current diagnostic and therapeutic approaches mainly rely on surgical resection and targeted therapy. However, early clinical diagnosis and resistance to targeted drugs remain the most challenging issues, severely compromising patient outcomes. Organoid technology can preserve patient-specific genotypic characteristics and drug sensitivity profiles in vitro, providing a novel platform for drug screening and investigation of resistance mechanisms; however, its application in GIST research remains at an early stage. Artificial intelligence (AI)-based radiomics, pathomics, large language models, and intelligent agents have demonstrated substantial potential in GIST risk stratification, genotype prediction, treatment response evaluation, and whole-lifecycle disease management. Integrating organoid model-derived data with multimodal clinical data through AI approaches and advancing the development of personalized decision-support systems represent emerging directions in precision diagnosis and treatment of GIST. The establishment of GIST organoid models is currently limited to case reports, with low culture success rates and prolonged drug sensitivity testing periods, making it difficult to meet the requirements of timely clinical decision-making. In contrast, AI applications in GIST imaging-based risk stratification and pathology-based genotype prediction have demonstrated preliminary high performance; however, most models still lack multicenter external validation, and their generalizability remains uncertain. Currently, the integration of AI and organoid technologies, including morphological quantitative assessment and virtual drug screening, relies mainly on methodological approaches developed in pan-cancer studies, with no studies directly investigating these approaches in GIST. Moreover, the development of multimodal decision-support systems faces major challenges, including data silos, insufficient algorithm interpretability, and the absence of clear regulatory pathways. Therefore, future efforts should focus on establishing standardized databases through multicenter collaboration and validating the clinical utility of integrated platforms through real-world studies, thereby facilitating the transition of these technologies from conceptual frameworks to clinical practice.

Indexed as

Artificial IntelligenceGastrointestinal NeoplasmsGastrointestinal Stromal TumorsOrganoidsPrecision MedicineHumansRadiomicsartificial intelligencedrug sensitivity testinggastrointestinal stromal tumormultimodal data fusionorganoidsvirtual screening

Identifiers

PMID42702375
PMCPMC13500748

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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.