A Study Using Cone Beam CT for Head and Neck Cancer
A Pilot Study of Tumor and Critical Normal Tissue Motion in Head and Neck Cancer Using Cone Beam CT
2 other identifiers
interventional
23
1 country
1
Brief Summary
Cone beam CT (computed tomography) is a developing technology which allows CT images to be obtained while a patient is on the radiation treatment table.(A CT scan uses x-rays to produce detailed pictures of structures in the body.) In this study, cone beam CT scans will be obtained before individual radiation treatment sessions for head and neck cancer. The information gathered from these scans will be used by the researchers to look at patient movement as well as changes in the amount of normal and tumor tissue throughout the course of radiation therapy. The researchers will use this information to create hypothetical radiation treatment plans, which will be used as the basis for future research. The cone beam CT scan data will not be used to alter the actual radiation treatment of any of the patients enrolled on the study. In addition, tests of salivary output and swallowing and questionnaires about quality of life will be made to assess how the doses of radiation affect them.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable head-and-neck-cancer
Started Jan 2009
Longer than P75 for not_applicable head-and-neck-cancer
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2011
CompletedFirst Submitted
Initial submission to the registry
September 26, 2011
CompletedFirst Posted
Study publicly available on registry
August 9, 2012
CompletedResults Posted
Study results publicly available
October 31, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2016
CompletedAugust 29, 2016
July 1, 2016
2.2 years
September 26, 2011
October 21, 2014
July 26, 2016
Conditions
Outcome Measures
Primary Outcomes (2)
Rate of Movement of Normal Tissue
The primary outcome measure of this study is to characterize patient-specific target and normal tissue movement.
approximately 7 weeks
Correlation Coefficient for the Association Between Delivered Mean Parotid Dose and Salivary Flow Rate
Spearman rank-based correlation coefficients were calculated for the association between saliva flow rate and the delivered mean parotid doses at several timepoints (Baseline, 3 months, 6 months, 12 months, 18 months, and 24 months).
24 months
Secondary Outcomes (2)
Improvement of Image Quality
36 months
The Median Delivered Dose of Radiation to the Parotid Gland
7 weeks
Study Arms (1)
Cone Beam CT
EXPERIMENTALAll patients will be included in the treatment arm of this study. For the purposes of this study patients will get CT scans every day for the length of their radiation therapy (in order to assess if CT every day provides additional information compared with CT scans performed less frequently). Although the exact amount of radiation patients get will be determined by their doctor, it is expected that they will get approximately 7 weeks, approximately 35 total cone beam CT scans.
Interventions
Cone beam CT scan is considered a noninvasive procedure (meaning that the procedure does not require breaking the skin or any tools that physically enter the body). It will add a small amount of additional radiation dose (less than 1%) to the head and neck. The increase in the amount of radiation is only a very small amount more than what patients who get standard daily imaging receive. The amount of radiation from the cone beam CT scans is not significant (less than 1%) when compared to the amount of radiation generally received for treatment of head and neck cancer.
Eligibility Criteria
You may qualify if:
- Patients of all ages ≥18, both sexes, and all races will be included in this study. Pregnant females will be excluded. No other special classes of subjects (i.e., prisoners) will be entered.
- Patients must be diagnosed with biopsy-proven squamous cell carcinoma of the head and neck.
- Patients must be recommended treatment with definitive radiation therapy with concurrent chemotherapy, but without prior surgical resection of the primary tumor or lymph nodes
- Patients must be recommended a treatment course of at least 30 radiation fractions
- Patients must sign an informed consent form approved for this purpose by the Institutional Review Board (IRB) of the University of Michigan Hospital indicating that they are aware that undergoing cone beam CT of the head and neck is voluntary and has potential risks.
You may not qualify if:
- Patients must not have a history of prior radiation to the head or neck
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Michigan Comprehensive Cancer Center
Ann Arbor, Michigan, 48109, United States
Related Publications (1)
Hunter KU, Fernandes LL, Vineberg KA, McShan D, Antonuk AE, Cornwall C, Feng M, Schipper MJ, Balter JM, Eisbruch A. Parotid glands dose-effect relationships based on their actually delivered doses: implications for adaptive replanning in radiation therapy of head-and-neck cancer. Int J Radiat Oncol Biol Phys. 2013 Nov 15;87(4):676-82. doi: 10.1016/j.ijrobp.2013.07.040. Epub 2013 Sep 10.
PMID: 24035328RESULT
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Avraham Eisbruch, M.D.
- Organization
- University of Michigan Comprehensive Cancer Center
Study Officials
- PRINCIPAL INVESTIGATOR
Avraham Eisbruch, MD
University of Michigan Rogel Cancer Center
Publication Agreements
- PI is Sponsor Employee
- Yes
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 26, 2011
First Posted
August 9, 2012
Study Start
January 1, 2009
Primary Completion
March 1, 2011
Study Completion
March 1, 2016
Last Updated
August 29, 2016
Results First Posted
October 31, 2014
Record last verified: 2016-07