Fluoroestradiol PET Imaging in Predicting Response to Hormone Therapy of Breast Cancer

Not Applicable

Completed

• Conditions: Metastatic Breast Cancer
• Interventions: Drug: Fluoroestradiol (18F)

• Registration Number: NCT01627704
• Lead Sponsor: Assistance Publique - Hôpitaux de Paris

Brief Summary

Compare the response rate after 6 months of hormone treatment (or a major change in hormone treatment) in metastatic breast cancer, according to the uptake of FES in metastatic lesions taking-up FDG on PET/CT at baseline. Hypothesis: best response rate will be observed in patients with all metastases taking up FES prior to treatment.

Detailed Description

Main objective: Compare the response rate after 6 months of hormone treatment (or a major change in hormone treatment) in metastatic breast cancer, according to the uptake of FES in metastatic lesions taking-up FDG on PET/CT at baseline.

Secondary objectives:

* evaluate diagnostic performance of FES PET/CT

* determine whether FES PET/CT is able to detect metastases that are not visible on FDG PET/CT. This point may constitute a direct benefit for the patient

* precise the nature of discordant FES/FDG foci

* validate and improve the interpretation criteria for FES PET/CT

* confirm the perfect tolerance

Study Timeline

• Study Start: 2012-06
• Study First Submitted: 2012-06-14
• Study First Submitted QC: 2012-06-25
• Study First Posted: 2012-06-26
• Primary Completion: 2015-01
• Study Completion: 2015-01
• Status Verified: 2015-10
• Last Update Submitted: 2015-10-13
• Last Update Posted: 2015-10-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 72

Inclusion Criteria

• Post menopausal
• age > 17
• WHO 0-2
• Metastatic adenocarcinoma of the breast
• Treated by antihormone treatment during around 5 years withdrawn for at least 3 months OR metastatic cancer at diagnosis having received no more than one line of hormone treatment
• Life expectancy > 6 months
• Hormone-dependent cancer initially demonstrated by hormone receptors in the tumour
• Presence of oestrogen receptors proven with immunohistochemistry (> 10%) and HER2 determined by immunohistochemistry or FISH (on primary tumour or a metastasis)
• Metastatic recurrence on FDG PET dating less than 1 month, confirmed by another modality (contrast-enhanced CT, MRI, ultrasonography, bone scintigraphy or PET/CT, other)
• FDG PET/CT available on PACS or CD DICOM III format 11
• Informed consent obtained

Exclusion Criteria

• Other evolutive malignant disease or acute or chronic infectious disease
• Chemotherapy during the last 3 months or change in treatment since FDG PET/CT.
• Isolated liver metastasis (high FES uptake by normal liver)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Fluoroestradiol (18F)	Fluoroestradiol (18F)	-

Primary Outcome Measures

Name	Time	Method
Response rate six months after induction or major change in hormone therapy for metastatic breast cancer.	at 6 months	Response rate six months after induction or major change in hormone therapy for metastatic breast cancer. Response will be determined according to RECIST 1.1 criteria for each patient.

Secondary Outcome Measures

Name	Time	Method
Number of visible non-physiologic foci on FES PET and on the corresponding FDG PET, during centralised reading sessions by masked readers.	at 6 months

Trial Locations

Locations (1)

Service de Médecine Nucléaire, Hôpital Tenon; 🇫🇷 Paris, France