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Breast Cancer Recurrence - the Accuracy of Dual-time PET/CT

Breast Cancer Recurrence - the Accuracy of Dual-time PET/CT

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01552655
Acronym
BREAC-AUT
Enrollment
101
Registered
2012-03-13
Start date
2011-12-31
Completion date
2014-12-31
Last updated
2015-04-21

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

Conditions

Breast Cancer Recurrent

Keywords

Dual-time PET/CT, Breast cancer recurrence, Bone scintigraphy, CT thorax upper abdomen

Brief summary

The purpose of this study is to elucidate the value of dual-time-point PET/CT in the recurrence of breast cancer and to determine whether the method is better than the modalities used in the standard work up. 150 patients with suspected breast cancer recurrence will be included. All patients will undergo dual-time-point PET/CT, CT of thorax and upper abdomen and bone scintigraphy. After completion of the examinations the early and the late PET/CT scan will be compared with each other, the diagnostic CT-scan and the bone scintigraphy. A verification of suspicious findings will be done by biopsy, if the area is accessible. If a biopsy cannot be obtained, the presence of recurrence will be verified with additional imaging follow-up to ensure the highest possible confidence. Sensitivity, specificity, accuracy, negative and positive predictive value (NPV/PPV) will be calculated for each modality (incl. early and late PET/CT).

Interventions

RADIATIONDual-time PET/CT (low-dose)

4 MBq/kg 18F-flour-deoxyglucose administered iv. PET/CT-scans performed 60 min and 180 min after injection.

Sponsors

Odense University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Clinical suspected recurrence of breast cancer * Blood glucose level less than 8,0 mmol/L

Exclusion criteria

* Disqualified patients * Other malignancies * \< 18 years * \< 50 kg * \> 90 kg * Pregnant or lactating * Patients with permanent address outside of the Region of Southern Denmark * Estimated inability to collaborate

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic value of dual-time point 18FDG PET/CT in recurrent breast cancer2 yearsThe sensitivity and specificity of dual-time point 18FDG PET/CT will be compared to conventional imaging modalities usually used in the work up of patients with suspected recurrent breast cancer. In this case CT of thorax and upper abdomen and bone scintigraphy.

Secondary

MeasureTime frameDescription
Diagnostic value of early and late 18FDG PET/CT respectively in recurrent breast cancer2 yearsThe sensitivity and specificity of early (60 min post injection) and late (180 min post injection) 18FDG PET/CT respectively in patients with suspected recurrent breast cancer.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026