Whole-body Magnetic Resonance Imaging (MRI) for Staging Malignant Lymphomas

Sponsor
UMC Utrecht (Other)
Overall Status
Completed
CT.gov ID
NCT00685997
Collaborator
ZonMw: The Netherlands Organisation for Health Research and Development (Other)
135
3
48
45
0.9

Study Details

Study Description

Brief Summary

Background:

The malignant lymphomas, Hodgkin´s disease (HD) and non-Hodgkin´s lymphoma (NHL), comprise approximately 5-6% of all malignancies in adults and account for 10% of childhood cancers. Once the diagnosis has been established histologically, extent of disease (staging) and response to therapy will be assessed by means of a computed tomography (CT) scan of the body. The staging at presentation is important for determining prognosis and choice of treatment. Unfortunately, CT is accompanied by a significant amount of radiation exposure which may induce second cancers. This is especially important in childhood, because rapidly dividing cells are more sensitive to radiation induced effects and children will have more years ahead in which cancerous changes might occur. New magnetic resonance imaging (MRI) techniques offer an alternative way for staging and follow-up of cancers, including the malignant lymphomas. Whole-body MRI (WB-MRI) is a radiation-free method which allows imaging of the body with excellent soft tissue contrast in a single examination.

Purpose:

The aim of this study is to examine if WB-MRI can replace CT in staging of patients with a malignant lymphoma.

Design:

This will be a multicenter, prospective, diagnostic cohort study (timeschedule: 36 months). 135 eligible patients will undergo WB-MRI on top of the protocolar imaging routinely done.

Study population:

Patients aged 8 years and older with a histological diagnosis of HD or NHL.

Statistical analysis:

The challenge of this study will be to show non-inferiority of WB-MRI compared to CT in staging malignant lymphoma. Testing of this hypothesis will be one-sided and performed using recently proposed techniques by Lui et al.

Radiation-related risk assessment:

A risk model will be used, based on the BEIR VII report, for modelling the late-term mortality from radiation induced tumors after exposure to ionizing radiation.

Economic evaluation:

Actual costs (from a societal perspective) will be determined for the two diagnostic tests. In case of clinical equivalence and similar costs or cost savings associated with MRI the latter can be considered dominant, obviating further economic evaluation. Otherwise, through modelling of expected long term health impact and associated outcomes such as quality of life and costs the incremental cost effectiveness will be evaluated.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    135 participants
    Observational Model:
    Cohort
    Time Perspective:
    Cross-Sectional
    Official Title:
    Whole-body MR Imaging for Staging Malignant Lymphomas
    Study Start Date :
    Jun 1, 2008
    Actual Primary Completion Date :
    Jan 1, 2012
    Actual Study Completion Date :
    Jun 1, 2012

    Outcome Measures

    Primary Outcome Measures

    1. The primary outcome will be the clinical stage according to WB-MRI findings and according to CT-findings. This clinical stage will be determined according to the Ann Arbor classification system. [December 2010]

    Secondary Outcome Measures

    1. The secondary outcome will be a (subjective) assessment of image quality and presence of artefacts, for both T1-weighted and T2-weighted MR images as well as CT. [December 2010]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    8 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • male or female patients

    • age: 8 years and older

    • histologically proven Hodgkin's disease or non-Hodgkin's lymphoma

    • patients scheduled for a CT of the body for initial staging

    • participant's parents (participant < 18 years) or the participant (participant >18 years) must willingly give written informed consent prior to the start of the study

    • whole-body MRI has to be performed within 10 days before or after CT, and before therapy has been started.

    Exclusion Criteria:
    • patients with a general contraindication for MRI (including cardiovascular pacemakers, claustrophobia)

    • patients who have had a previous malignancy

    • patients who are pregnant or nursing

    • patients in whom therapy has already started after CT and before MRI could be performed

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Academic Medical Center Amsterdam Amsterdam Noord-Holland Netherlands 1105 AZ
    2 Meander Medical Center Amersfoort Amersfoort Utrecht Netherlands 3818 ES
    3 University Medical Center Utrecht Utrecht Netherlands 3584 CX

    Sponsors and Collaborators

    • UMC Utrecht
    • ZonMw: The Netherlands Organisation for Health Research and Development

    Investigators

    • Principal Investigator: Rutger A. J. Nievelstein, MD PhD, UMC Utrecht

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    R.A.J. Nievelstein, M.D., Ph.D., UMC Utrecht
    ClinicalTrials.gov Identifier:
    NCT00685997
    Other Study ID Numbers:
    • 80-82310-98-08012
    First Posted:
    May 29, 2008
    Last Update Posted:
    Jul 3, 2013
    Last Verified:
    Jul 1, 2013
    Keywords provided by R.A.J. Nievelstein, M.D., Ph.D., UMC Utrecht
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 3, 2013