MRI in Predicting Early Response to Chemotherapy in Patients With Locally Advanced Breast Cancer

Breast Cancer Clinical Trial

Official title:

Neo Comice Pilot; Efficacy of Advanced Semi-automated Functional Magnetic Resonance (MR) Imaging in the Early Prediction of Response of Locally Advanced Breast Cancer to Neoadjuvant Chemotherapy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00978770
• Other study ID #: CCTU-Neo-COMICE
• Secondary ID: CDR0000649054ISR
• Status: Completed
• Phase: Phase 2
• First received: September 16, 2009
• Last updated: August 6, 2013
• Start date: August 2009
• Est. completion date: January 2010

Study information

• Verified date: September 2009
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: Unspecified
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Diagnostic procedures such as MRI scans may help predict early response to treatment in patients with breast cancer undergoing chemotherapy.

PURPOSE: This phase II trial is studying MRI in predicting early response to chemotherapy in patients with locally advanced breast cancer.

Description:

OBJECTIVES:

• To determine the technical feasibility of using MRI in a multicenter setting using the most commonly available magnetic resonance (MR) systems (i.e., is the trial able to scan patients to a specific protocol, using different types of MRI machine) measured by the number of MRI scans not completed to technical specifications (i.e., incorrect sequences or incomplete scans) or trial protocol (i.e., scans not completed or completed at the wrong time).

• To determine how reliably the imaging data can be analyzed in a centralized, semi-automated manner (i.e., can MRI data be reliably transferred from different centers and analyzed using software based in the center for MR investigations at the University of Hull) measured by the number of cases where automated data analysis of completed MRI scans was not possible (i.e., data could not be analyzed at all or data required manual analysis).

OUTLINE: This is a multicenter study.

Patients undergo magnetic resonance imaging (MRI) scans at baseline, 4-7 days after beginning after the first course of chemotherapy, at the end of their second course of chemotherapy, and at the end of their fourth course of chemotherapy (first regimen). MRI techniques may include dynamic contrast-enhanced, diffusion-weighted, and spectroscopic.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: January 2010
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Newly diagnosed, histologically proven breast cancer

• Stage T2-4B, N0-3C, and M0 disease

• Locally advanced primary disease

• Underwent both x-ray mammography and breast ultrasound scanning during the current treatment episode

• Scheduled for neoadjuvant chemotherapy

PATIENT CHARACTERISTICS:

• Not pregnant or nursing

• Medically stable

• No renal failure

• No serious breast trauma within the past 3 months

• No known allergic reaction associated with previous administration of a paramagnetic contrast agent

• No known contraindication to magnetic resonance (MR) scanning

• Must pass the normal safety requirements of MR, particularly pacemakers and cardiac defibrillators

• No disability preventing MR scanning in the prone position

• No body habitus incompatible with MR system entry

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics

• No prior chemotherapy

• No prior surgery or radiotherapy for cancer in the ipsilateral breast

• More than 4 months since prior surgery to the ipsilateral breast for benign breast disease

Study Design

Primary Purpose: Diagnostic

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Drug:
• systemic chemotherapy

Procedure:
• diffusion-weighted magnetic resonance imaging

• dynamic contrast-enhanced magnetic resonance imaging

• magnetic resonance spectroscopic imaging

• neoadjuvant therapy

Locations

Country	Name	City	State
United Kingdom	Cactus Clinical Trials Unit	Hull	England

Sponsors (1)

Lead Sponsor	Collaborator
Cancer Clinical Trials Unit, Scotland

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Failed scan rate (i.e., the number of scans that failed protocol) grouped by cause, including patient refusal, protocol violation in timing, major errors in scan protocols, and minor errors in scan protocol			No
Primary	Failed automated MRI-scan data-analysis rate (i.e., number of scans that required manual reading and number of protocol-compliant scans that were unreadable, subdivided according to whether the scans were technically compliant or not)			No