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The Performance of Multi-tracer Multimodality PET in Lymphoma

The Performance of Multi-tracer Multimodality PET in Lymphoma

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05004961
Enrollment
200
Registered
2021-08-13
Start date
2019-09-15
Completion date
2023-12-31
Last updated
2023-03-03

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

Conditions

Positron-Emission Tomography

Keywords

Positron-Emission Tomography, Lymphoma

Brief summary

Investigating the performance of Multi-tracer Multimodality PET in lymphoma

Detailed description

In this study investigators evaluated Nodal and Extranodal Lymphoma Lesions uptake by different molecular probe such as FDG, FAPI-04 via multimodality PET (PET/CT and PET/MR). Our Previous studies have shown that uptake of FAPI-04 on PET may be an indicator of lymphoma lesions. The combination of PET with CT/MR allows for depicting metabolic, functional and morphological properties of tumor lesions at the same time, which is therefore an alternative attractive pairing for diagnosis, staging and prognosis of lymphoma.

Interventions

None listed

Sponsors

Peking University Cancer Hospital & Institute
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* pathologically diagnosed as lymphoma; * Written informed consent for receiving FAPI-04 PET examinations. * cancer planned chemotherapy or immunotherapy scheme. * expected survival ≥ 12 weeks

Exclusion criteria

* cannot lie supine for half an hour; * refuse to join the clinical researcher; * severe liver or kidney dysfunction * pregnancy or lactation

Design outcomes

Primary

MeasureTime frameDescription
SUVmax150 daysStandardized uptake value of 68Ga/ 18F-NOTA-FAPI 04 for target lesion of subject or suspected tumor in each time point window (SUV)

Countries

China

Contacts

Primary ContactXuejuan Wang, MD
xuejuan_wang@hotmail.com86 010 88196363

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026