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Active, not recruitingNCT07890038Updated Oct 22, 2026

The Clinical Application Value of CAIX-Targeted PET Hypoxia Imaging in Malignant Tumors

An observational study in Nasopharyngeal Cancers, Lung Cancer (NSCLC) and Esophageal Cancer, sponsored by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology. Active, not recruiting at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-22.

Sponsored by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · Observational

Updated Oct 22, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
50
Ages
18 Years and older
Sex
All
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Study summary

This project involves conducting integrated PET/MR or PET/CT imaging using a CAIX-targeted PET tracer (e.g., [68Ga]Ga-DOTA-CAIX peptide) in clinically diagnosed malignant tumor patients, aiming to achieve the following objectives:

Patients with malignant tumors: To visually assess the hypoxic state of malignant tumors, with pathological immunohistochemical detection of CAIX expression levels as the gold standard, evaluate the detection efficacy and quantitative accuracy of CAIX PET imaging for tumor hypoxic regions; clarify the location, extent, and heterogeneous distribution characteristics of hypoxic subregions within tumors; conduct a head-to-head comparison with [18F]FDG PET imaging to assess the complementary value and differences of the two imaging techniques in tumor boundary delineation, metastatic lesion detection, and tumor burden evaluation; based on the hypoxic biological information provided by CAIX PET imaging, assist clinicians in designing hypoxia-conformal margin expansion for radiotherapy target volumes, aiding in the determination of personalized radiotherapy and combined treatment plans.

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Conditions studied

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In context

Nasopharyngeal Neoplasms

242 studies on the registry are indexed under Nasopharyngeal Neoplasms; 47 are open to participants now.

This study's planned enrollment of 50 is below the median of 132 across 38 observational studies indexed under Nasopharyngeal Neoplasms.

Browse Nasopharyngeal Neoplasms studies →

Lead sponsor

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology is the lead sponsor of 172 studies on the registry; 136 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients with clinically suspected or diagnosed malignant diseases, such as lung cancer, nasopharyngeal cancer, esophageal cancer, glioma, etc. (supported by evidence including serum tumor markers, ultrasound, CT, MRI, and histopathological examinations), have an overall good condition.

Eligibility criteria

All baseline subjects who meet any exclusion criteria will be excluded from the study (1) Individuals who are unable to complete PET/MR or PET/CT examinations (including inability to lie flat, claustrophobia, radiation phobia, etc.); (2) Having other comorbidities; (3) Patients known to be allergic to targeted CAIX PET imaging agents or synthetic excipients; Fasting blood glucose levels exceeding 11.0 mmol/L before injection of [18F] FDG; (4) Having a history of concomitant medication; (5) Researchers believe that patients with poor compliance; (6) Pregnant or lactating patients; (7) Individuals with other factors that are not suitable for participating in this experiment.

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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
50 participants (estimated)
Patient registry
No

Interventions

  • Diagnostic testSpecific PET Imaging Agent Targeting CAIX

    This project utilizes CAIX specific targeted PET radiotracer to perform PET/CT imaging on healthy volunteers and clinically suspected or diagnosed patients with malignant tumors such as lung cancer, nasopharyngeal cancer, esophageal cancer, glioma, etc

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What researchers measure

Primary outcomes

  1. Visual and standardized uptake values assessment of lesions and biodistribution

    At least two experienced nuclear medicine physicians will conduct a visual analysis using consensus reading. The standardized uptake value (SUV) of the tumor and organs will be measured after a semiquantitative analysis is performed for each case. The SUV ranges from 0 to infinity, and a higher score means a higher uptake of targeting LRRC15 nuclear probe by the tumor, which implies a greater threat of the tumor being malignant or a higher stage.

    Time frame: 1 year

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Study locations

1 site
  • Department of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei Province, China.
    Wuhan, 430000, China
08

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 22, 2026
Show all 1 update
  1. Oct 22, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

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Registry details

Key details

Study ID
NCT07890038
Responsible party
Sponsor
First posted
Oct 22, 2026
Start date
Jun 11, 2026
Primary completion
Jun 30, 2027 (estimated)
Completion
Jun 30, 2027 (estimated)
Last update
Oct 22, 2026

Oversight

FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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