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Study on the Application of 18F-FMISO PET/CT and 18F-FAPI PET/CT Imaging in the Evaluation of the Efficacy of Induction Chemotherapy and Concurrent Chemoradiotherapy for Locally Advanced Nasopharyngeal Carcinoma

Study on the Application of 18F-FMISO PET/CT and 18F-FAPI PET/CT Imaging in the Evaluation of the Efficacy of Induction Chemotherapy and Concurrent Chemoradiotherapy for Locally Advanced Nasopharyngeal Carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127070
Enrollment
Unknown
Registered
2026-06-24
Start date
2026-06-24
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Locally advanced nasopharyngeal carcinoma

Interventions

Gold Standard:The reference standard is the contrast-enhanced MRI of the head and neck performed at 3 months after the completion of concurrent chemoradiotherapy, evaluated according to the RECIST 1.1
Index test:The semi-quantitative parameters (TMR, TBR, SUVmax, SUVmean, MTV, TLG, etc.) obtained from 18F-FMISO PET/CT, 18F-FAPI PET/CT and 18F-FDG PET/CT before treatment were used as the index tests

Sponsors

Affiliated Tumor Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Pathologically confirmed as nasopharyngeal squamous cell carcinoma, with UICC/AJCC 9th edition staging of anyTN3M0 or T4N0-3M0; 2.Patients with an ECOG performance status score of 0-1 can tolerate radiotherapy, chemotherapy, and imaging examinations; 3.There was no previous history of other tumors, and no anti-tumor treatment had been received. 4.Voluntarily participate in this study and sign the written informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients with a history of other malignant tumors were excluded; 2.Patients who did not complete the full treatment course or withdrew midway were excluded; 3.Patients with severe organ dysfunction and inability to cooperate with examinations were excluded;

Design outcomes

Primary

MeasureTime frame
Progression-Free Survival;Objective Response Rate;

Secondary

MeasureTime frame
PET quantitative and semi-quantitative parameters;

Countries

China

Contacts

Public ContactHai Liao

Affiliated Tumor Hospital of Guangxi Medical University

42442427@qq.com+86 771 577 6082

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 3, 2026