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Evaluation of the use of PET/CT in Adenoid Cystic Carcinoma (ADC)

Evaluation of the use of PET/CT with 18F-PSMA as a staging tool and potential predictor for theranostic therapy in patients diagnosed with Adenoid Cystic Carcinoma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
REBEC
Registry ID
RBR-84nmnm9
Enrollment
Unknown
Registered
2023-07-31
Start date
2023-05-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Adenoid Cystic Carcinoma

Interventions

Single-center, prospective study, which will be carried out in the Departments of Nuclear Medicine, Clinical Oncology and Head and Neck Surgery at the A.C.Camargo Cancer Center. It is estimated that a
V03.175.500

Sponsors

Eduardo Nóbrega Pereira Lima
Lead Sponsor
Fundação Antônio Prudente - AC Camargo Cancer Center
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age above 18 years. Histological diagnostic confirmation of Neoplasia Adenoid Cystic Carcinoma (ADC). Ability to understand aspects associated with the proposed clinical study and consent to participate.Patients who have performed at least one onventional imaging (computed tomography, magnetic resonance imaging, ultrasonography, and bone scintigraphy) as part of an initial assessment of the extent of neoplastic disease or as part of a recent assessment of ongoing tumor response to CAdC neoplasia.

Exclusion criteria

Exclusion criteria: Clinical condition that contraindicates the use of targeted imaging for staging conventional or exposure to radiopharmaceuticals such as: ongoing pregnancy, breastfeeding or any condition that the attending physician considers a risk for participation in the study.

Design outcomes

Primary

MeasureTime frame
To present prospective controlled data on the use of PET/CT with 18F-PSMA in patients with CAD, using an isotope that is widely available in our routine, which may have a direct impact on the management of therapeutic

Secondary

MeasureTime frame
No secondary outcomes expected

Countries

Brazil

Contacts

Public ContactAndre Ribeiro

AC Camargo Cancer Center

andre.ribeiro@accamargo.org.br+55(11)21895000 - Ramal 2832

Outcome results

None listed

Source: REBEC (via WHO ICTRP)