Evidence map›Paper›PMID 42638115›Full record

ArticleBiomarker research2026

Immuno-PET imaging of mesothelin in ovarian cancer with

Yueling Deng, Xiao Zhang, Zhidi Pan, Xiaoying Lv, Zhaoguo Lin, Yuan Feng, Zaijie Wu, Xiangming Song, Yongkang Gai, Haiyang Yin and 3 more

Registry-linked trialAbstract read
In one paragraph

Article in Biomarker research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06843629 (Clinical Application of PET Imaging Targeting MSLN in Malignant Tumors), which is not on this 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.

NCT06843629 recruitingnot on this map

Clinical Application of PET Imaging Targeting MSLN in Malignant Tumors

TypeobservationalSponsorUnion Hospital, Tongji Medical College, Huazhong University of Science and TechnologyRan2024 to 2028Enrolled100ConditionsOvarian Cancer, Lung Adenocarcinoma, Pancreatic CancerArmsSpecific positron imaging agents targeting MSLN
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

13 authors.

Yueling Deng *Department of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1277 Jiefang Avenue, Wuhan, Hubei Province, 430022, China.
Xiao Zhang *Department of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1277 Jiefang Avenue, Wuhan, Hubei Province, 430022, China.
Zhidi PanJecho Institute, Shanghai, 200240, China.
Xiaoying LvDepartment of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1277 Jiefang Avenue, Wuhan, Hubei Province, 430022, China.
Zhaoguo LinDepartment of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1277 Jiefang Avenue, Wuhan, Hubei Province, 430022, China.
Yuan FengDepartment of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1277 Jiefang Avenue, Wuhan, Hubei Province, 430022, China.
Zaijie WuDepartment of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1277 Jiefang Avenue, Wuhan, Hubei Province, 430022, China.
Xiangming SongDepartment of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1277 Jiefang Avenue, Wuhan, Hubei Province, 430022, China.
Yongkang GaiDepartment of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1277 Jiefang Avenue, Wuhan, Hubei Province, 430022, China.
Haiyang YinJecho Institute, Shanghai, 200240, China.
Jianwei ZhuJecho Institute, Shanghai, 200240, China.
Dawei JiangDepartment of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1277 Jiefang Avenue, Wuhan, Hubei Province, 430022, China. daweijiang@hust.edu.cn.ORCID https://orcid.org/0000-0002-4072-0075
Xiaoli LanDepartment of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1277 Jiefang Avenue, Wuhan, Hubei Province, 430022, China. lxl730724@hotmail.com.ORCID http://orcid.org/0000-0002-7263-7399

Funding

Hubei Province Science and Technology Innovation Team [2022] No. 72National Natural Science Foundation of China No. 82030052
6 · The paper itself

Abstract

backgroundMesothelin is highly expressed in ovarian cancer and represents a promising target for precision imaging and therapy. This study aimed to develop and evaluate ⁶⁸Ga-XH04, a novel mesothelin-targeted immuno-PET tracer for non-invasive imaging of mesothelin expression in preclinical models and patients.

methodsXH04, a high-affinity anti-mesothelin antigen-binding fragment (Fab), was engineered and conjugated with NOTA for radiolabeling with ⁶⁸Ga. Binding affinity and specificity were assessed in vitro using cell lines with graded mesothelin expression. In vivo PET imaging, biodistribution, and pharmacokinetics were evaluated in xenograft models. Immunohistochemistry was performed to correlate tracer uptake with mesothelin levels. A first-in-human pilot study was conducted in a healthy volunteer and ovarian cancer patients to assess safety, imaging characteristics, and descriptive comparison with ¹⁸F-FDG PET/CT.

results⁶⁸Ga-XH04 exhibited high radiochemical purity (> 98%) and nanomolar affinity for mesothelin. In preclinical models, ⁶⁸Ga-XH04 showed rapid clearance and higher uptake in mesothelin-high xenografts than in mesothelin-low xenografts, supporting exploratory assessment of mesothelin-dependent tracer accumulation. Immunohistochemistry confirmed the correlation between tracer uptake and mesothelin expression. In patients, ⁶⁸Ga-XH04 was well tolerated and visualized primary and metastatic lesions. In this preliminary cohort, ⁶⁸Ga-XH04 provided information complementary to ¹⁸F-FDG PET/CT and identified lesions with relatively low FDG uptake.

conclusion⁶⁸Ga-XH04 demonstrated the feasibility of specific, noninvasive, and high-contrast imaging of mesothelin expression in ovarian cancer with favorable pharmacokinetics. This tracer may complement existing imaging modalities by enabling noninvasive assessment of mesothelin expression and may provide imaging-based information to support future investigation of mesothelin-targeted therapies. Larger prospective studies are required to validate its diagnostic value and clinical utility.

trial registrationClinicalTrials.gov (NCT06843629); registered on December 20, 2024.

Indexed as

Fab fragmentImmuno-PETMesothelinMolecular imagingOvarian cancer

Identifiers

PMID42638115
PMCPMC13501770

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