Imaging Evaluation of the Therapeutic Response of Breast Cancer Bone Metastasis (EMOS)

NCT ID: NCT02900118

Last Updated: 2016-09-14

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 28 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2012-08-31
• Study Completion Date: 2013-10-31

Brief Summary

Breast cancers are among the cancers that metastasize the most to the skeleton. The appearance of bone metastasis, whether they are initials or during a relapse, is a turning point of the disease, due to the additional morbidity they imply (pain, pathologic fractures, hypercalcaemia, neurological compression, etc.). A specific treatment of these metastasis is often undertaken, usually a chemotherapy or hormone therapy. It is important to evaluate the efficacy of this treatment in order to know whether to continue or change it depending on the response observed. But there is no consensus at this time on paraclinical examinations enabling this monitoring. Also, if some criteria for assessing bone metastasis in imaging and nuclear medicine (MDA, PERCIST, EORTC) have been published in the literature, none is formally validated and evaluation in routine practice remains subjective.

The main objective of our study is to determine if the PET-CT and the whole-body MRI are in agreement on the status of bone metastasis (stability, progression, partial response, complete response).

Detailed Description

The oncologist includes patients responding to criteria and not opposing the collection of their data. He submits a request for whole-body MRI and PET-CT to the Medical Imaging and Nuclear Medicine departments of the Oscar Lambret Centre. If the patient has benefited within the previous 15 days of any of these examinations, it is not performed again : it will serve as an initial examination. Following these examinations, the oncologist completes the reading grid. A clinical examination and a questioning with the main stages of the disease is performed and data are reported in the dedicated sheet. A prescription of tumor markers and of bone remodeling is performed (in the absence of recent results), and the results are reported on the same sheet.

After 3 cycles (of intravenous chemotherapy) or 3 months of hormone therapy, the oncologist submits a new request for whole-body MRI and PET-CT. The MRI and PET-CT should conclude to a status : progression, stability, partial response, complete response. The reading grid is completed again. MDA criteria (MRI and PET-CT), PERCIST and EORTC (PET-CT only) are determined. Target lesions (1 to 3) are defined for each examination and a measure of the ADC and the SUV is performed for each lesion on the initial and follow-up examinations.

After these examinations, the patient is reviewed by his oncologist for a new clinical examination, the announcement of the status of bone metastasis and the possible adaptation of the treatment.

Conditions

Breast Cancer

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Group 1

Patients with breast cancer bone metastasis at the initial diagnosis.

No interventions assigned to this group

Group 2

Patients with breast cancer bone metastasis in a metastatic bone relapse.

No interventions assigned to this group

Group 3

Patients with breast cancer bone metastasis with a progression of bone metastasis.

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

1. Patient with breast cancer bone metastasis :

• at the initial diagnosis (group 1).
• in a metastatic bone relapse (group 2).
• with a progression of bone metastasis (group 3).

2. Treatment (hormone therapy, chemotherapy) not undertaken (group 1) or prior therapeutic change (group 2 and 3).

3. Patient not opposing the use of its data.

Exclusion Criteria

1. Claustrophobic patient

2. Patient with an uncontrolled diabetes (fasting glucose < 1.6 g / l)

3. Patient with a pace-maker or another material incompatible with the MRI 3 Tesla

4. Very algetic patient (Visual Analog Scale (VAS) > 7)

5. Pregnant or breastfeeding women

6. Patient under 18 or under guardianship

7. Movement disorders (Parkinson disease, etc.) or dementia

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Centre Oscar Lambret

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Armelle RENAUD, MD

Role: PRINCIPAL_INVESTIGATOR

Centre Oscar Lambret

Locations

Centre Oscar Lambret

Lille, , France

Countries

France

Other Identifiers

EMOS-1207

Identifier Type: -

Identifier Source: org_study_id