Dynamic Contrast-Enhanced Magnetic Resonance Imaging in Diagnosing Osteoradionecrosis in Patients With Head and Neck Cancer That Is Primary, Has Come Back, or Has Spread to Other Places in the Body

Sponsor

M.D. Anderson Cancer Center (Other)

Overall Status

Recruiting

CT.gov ID

NCT03145077

Collaborator

National Cancer Institute (NCI) (NIH), National Institute of Dental and Craniofacial Research (NIDCR) (NIH)

1,400

Enrollment

Location

Arms

60.3

Anticipated Duration (Months)

23.2

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This trial studies how well dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) works in diagnosing osteoradionecrosis in patients with head and neck cancer that is primary, has come back, or has spread to other places in the body who are undergoing radiation therapy. DCE-MRI may help doctors to predict osteoradionecrosis in patient with head and neck cancer undergoing radiation therapy.

Condition or Disease	Intervention/Treatment	Phase
Head and Neck Cancer	Procedure: Dynamic Contrast-Enhanced Magnetic Resonance Imaging Other: Questionnaire Administration	N/A

Detailed Description

PRIMARY OBJECTIVES:

To determine whether DCE-MRI following external beam radiation therapy (EBRT) can be used to reliably predict osteoradionecrosis (ORN).

SECONDARY OBJECTIVES:

Define dose-response relationships between DCE-MRI derived imaging biomarkers and subsequent development of ORN.
Evaluate the use of DCE-MRI parameters to monitor ORN response to treatment.
Assess the use of DCE-MRI parameters in preoperative planning in advanced ORN subjects.
Develop MRI-based biomarkers inclusive predictive models for development of radiotherapy-attributable tissue injury within the field of radiation.
Determine the association of patient-related outcomes (PROs) to clinical and imaging findings of tissue damage, such as the onset of ORN.

OUTLINE: Patients are assigned to 1 of 4 cohorts.

COHORT 1: Patients with newly diagnosed tumors undergo DCE-MRI within 4 weeks prior to the first radiation fraction, within 3-5 weeks after radiation start, and at 2, 6, 12, 24, and 36 months post radiation. Patients who were previously irradiated and are at various stages of oncologic follow-up undergo DCE-MRI for a total of 2-5 times at baseline and at 6, 12, 24, 36, and/or 48 months post radiation. Patients in the third or subsequent years post treatment may undergo subsequent yearly imaging studies.

COHORT 2: Patients undergo DCE-MRI within 4 weeks prior to the first re-radiation fraction, within 3-5 weeks after radiation start, and at 2, 6, 12, 24, and 36 months post radiation.

COHORT 3: Patients undergo DCE-MRI before and at 2 and 6 months post ORN treatment. Patients may undergo DCE-MRI during the mid-ORN treatment.

COHORT 4: Patients undergo DCE-MRI within 4 weeks prior to and at 5-10 weeks and 12 months post surgery.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

1400 participants

Allocation:

Non-Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Diagnostic

Official Title:

Using Magnetic Resonance Imaging (MRI) to Assess Mandibular and Soft Tissue Responses to Radiation Therapy

Actual Study Start Date :

Mar 21, 2017

Anticipated Primary Completion Date :

Mar 31, 2022

Anticipated Study Completion Date :

Mar 31, 2022

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Cohort 1 (DCE-MRI) Patients with newly diagnosed tumors undergo DCE-MRI within 4 weeks prior to the first radiation fraction, within 3-5 weeks after radiation start, and at 2, 6, 12, 24, and 36 months post radiation. Patients who were previously irradiated and are at various stages of oncologic follow-up undergo DCE-MRI for a total of 2-5 times at baseline and at 6, 12, 24, 36, and/or 48 months post radiation. Patients in the third or subsequent years post treatment may undergo subsequent yearly imaging studies.	Procedure: Dynamic Contrast-Enhanced Magnetic Resonance Imaging Undergo DCE-MRI Other Names: DCE MRI DCE-MRI DYNAMIC CONTRAST ENHANCED MRI Other: Questionnaire Administration Ancillary studies
Experimental: Cohort 2 (DCE-MRI) Patients undergo DCE-MRI within 4 weeks prior to the first re-radiation fraction, within 3-5 weeks after radiation start, and at 2, 6, 12, 24, and 36 months post radiation.	Procedure: Dynamic Contrast-Enhanced Magnetic Resonance Imaging Undergo DCE-MRI Other Names: DCE MRI DCE-MRI DYNAMIC CONTRAST ENHANCED MRI Other: Questionnaire Administration Ancillary studies
Experimental: Cohort 3 (DCE-MRI) Patients undergo DCE-MRI before and at 2 and 6 months post ORN treatment. Patients may undergo DCE-MRI during the mid-ORN treatment.	Procedure: Dynamic Contrast-Enhanced Magnetic Resonance Imaging Undergo DCE-MRI Other Names: DCE MRI DCE-MRI DYNAMIC CONTRAST ENHANCED MRI Other: Questionnaire Administration Ancillary studies
Experimental: Cohort 4 (DCE-MRI) Patients undergo DCE-MRI within 4 weeks prior to and at 5-10 weeks and 12 months post surgery.	Procedure: Dynamic Contrast-Enhanced Magnetic Resonance Imaging Undergo DCE-MRI Other Names: DCE MRI DCE-MRI DYNAMIC CONTRAST ENHANCED MRI Other: Questionnaire Administration Ancillary studies

Outcome Measures

Primary Outcome Measures

DCE-MRI Derived Parameters Following External Beam Radiation Therapy (EBRT) and Subsequent Development of Osteoradionecrosis (ORN) [5 years]
Spatiotemporal parameter maps extracted from patient DCE-MRI scans. Clinical staging of developing or existing ORN conducted according to the CTCAE 4.0.

Secondary Outcome Measures

Dose-Response Relationships Between DCE-MRI Derived Imaging Biomarkers and Subsequent Development of Osteoradionecrosis (ORN) [5 years]
Voxel-by-voxel correlation of delivered radiation dose to mandible and DCE-MRI parameter changes determined to establish a dose-biomarker response relationship.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Willing and able to provide informed consent
Patients must have histologic evidence of malignant neoplasm that may have been obtained from the primary tumor or metastatic lymph node
Receipt of external beam radiation therapy (EBRT) with curative intent, with or without concomitant chemotherapy
Good performance status (Eastern Cooperative Oncology Group [ECOG] score 0-2)
Willing to comply with all study procedures; and
Willing to participate for the duration of the study
COHORT 1 (LONGITUDINAL) GROUP 1 (PRE-RADIATION): Subjects who are currently undergoing or scheduled to undergo treatment with radiotherapy with or without chemotherapy (induction or concurrent) with intent to eradicate the malignancy. Treatment will include the following: 1) primary or nodal disease adjacent to (within 2 cm) the mandible (i.e., likely to receive a dose of at least 50 Gy to some portion of the mandible volumes) and 2) > 60% probability of survival for 3 years after treatment
COHORT 1 (LONGITUDINAL) GROUP 2 (POST-RADIATION): Subjects who were previously treated with radiotherapy with or without chemotherapy (induction or concurrent). Treatment will have included the following: 1) unilateral maximum mandible dose of >= 60 Gy and a gradient of dose across the mandible of >= 20 Gy, 2) oncological cure and now in disease surveillance; and 3) no clinically diagnosed ORN at the time of enrollment
COHORT 2 (ENRICHED): Subjects with recurrent and/or new head and neck cancer disease who will undergo re-irradiation to the head and neck with intent to eradicate the malignancy. Treatment will include the following: 1) any mandible dose of at least 50 Gy cumulative (initial and subsequent treatment); and 2) no clinically diagnosed ORN at the time of enrollment
COHORT 3 (EARLY ORN INTERVENTION): Subjects with clinically confirmed low-grade/early stage osteoradionecrosis requiring therapeutic (medical and/or dental surgery) intervention as diagnosed by a qualified clinician. Clinical staging of developing or existing ORN will be conducted using the CTCAE 4.0 (Common Terminology Criteria for Adverse Events)
COHORT 4 (SURGICAL INTERVENTION FOR ADVANCED ORN): Subjects with clinically confirmed high grade/high stage osteoradionecrosis requiring surgical intervention. Clinical staging of ORN will be conducted using the CTCAE 4.0 (Common Terminology Criteria for Adverse Events)

Exclusion Criteria:

Unable to tolerate diffusion weighted (DW)-MRI or DCE-MRI
Having an estimated glomerular filtration rate (GFR) < 60 ml/min/1.73 m^2
Contraindication to MRI (e.g. non-MRI compatible metallic implants)
Pregnant females
Unable or unwilling to give written, informed consent to undergo MRI imaging
Claustrophobia
Unable to obtain imaging studies of adequate quality to assess imaging-based biomarkers
COHORT 1/GROUP 1: Previously treated with radiotherapy for a malignant neoplasm of the head and neck, excluding cutaneous lesions. Determination will be made by review of the radiation therapy plan and dosimetry map to evaluate mandible exposure to radiation
COHORT 1/GROUP 2: Previously treated with radiotherapy for a malignant neoplasm of the head and neck more than one time, excluding cutaneous lesions