Skip to content

Clinical application of PET / CT imaging targeting tumor associated fibroblast activating protein (FAP) in solid tumors

Clinical application of PET / CT imaging targeting tumor associated fibroblast activating protein (FAP) in solid tumors

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000039099
Enrollment
Unknown
Registered
2020-10-17
Start date
2020-10-19
Completion date
Unknown
Last updated
2021-01-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tumors

Interventions

Gold Standard:Pathologic diagnosis
Index test:1.&#32
CT&#32
imaging&#32
tumor&#32
activating&#32
protein&#32
(FAP) 2.&#32

Sponsors

Department of Nuclear Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients aged 18-80 years old, male or female; 2. Subjects with solid tumors or suspected tumors who plan to undergo pathological biopsy or tumor surgery in the near future (within 2 months); 3. Patients with expected survival >= 12 weeks; 4. Patients whose blood routine and liver and kidney function meet the following criteria: blood routine: WBC >= 4.0 x 10^9/L or neutrophil >= 1.5 x 10^9/L, PLT >= 100 x 10^9 /L, Hb >= 90g /L; PT or APTT <= 1.5 ULN; liver and kidney function: T-Bil <= 1.5 x ULT (upper limit of normal value), ALT / AST <= 2.5 ULN or <= 5 x ULT (liver metastasis subjects), ALP <= 2.5 ULN(if there is bone metastasis or liver metastasis, ALP <= 4.5uln), bun <= 1.5 x ULT, SCR <= 1.5 x ULT; 5. Patients with at least one measurable target lesion according to recist1.1; 6. Patients who understand and sign informed consent voluntarily.

Exclusion criteria

Exclusion criteria: 1. Patients with severe abnormal liver and kidney function; 2. Pregnant, pregnant and lactating women; 3. Patients who cannot lie on their back for half an hour; 4. Patients with claustrophobia or other mental diseases; 5. Other researchers think that it is not suitable to participate in the trial.

Design outcomes

Primary

MeasureTime frame
SUVmax;SEN, SPE, ACC, AUC of ROC, PPV, NPV;

Countries

China

Contacts

Public ContactXiaohua Zhu

Tongji Hospital Affiliated to Tongji Medical College of Huazhong University of Science and Technology

evazhu@vip.sina.com+86 13971513770

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026