Intensity-Modulated or Proton Radiation Therapy for Sinonasal Malignancy
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|ClinicalTrials.gov Identifier: NCT01586767|
Recruitment Status : Recruiting
First Posted : April 27, 2012
Last Update Posted : September 21, 2018
The purpose of this study is to test the hypothesis that 1)intensity-modulated radiotherapy (IMRT) or proton radiation therapy would result in improved local control rate and lowered toxicity compared to conventional radiotherapy, and 2) proton radiation therapy would result in equivalent or improved local control rate with similar or lower toxicity compared to IMRT, in the treatment of locally advanced sinonasal malignancy.
Data from retrospective studies suggest that IMRT or proton radiation therapy resulted in promising outcome in patients with sinonasal malignancy. To this date, no prospective study has been conducted to evaluate the outcome of sinonasal cancer treated with IMRT or proton radiation therapy. This Phase II trial is the first prospective study conducted to determine the treatment outcome and toxicity of IMRT or proton in the treatment of sinonasal cancer.
IMRT and proton radiation therapy are the two most established and most commonly employed advanced radiotherapy techniques for the treatment of sinonasal cancer. It is highly controversial whether one is superior to the other in terms of local control and toxicity outcome. It is also not clear if a subset of patients would benefit more from one treatment technology versus the other.
Due to the rarity and heterogeneity of sinonasal malignancies and the fact that proton beam is only available at a few centers in the United States, it is not feasible at present to do a Phase III study randomizing patients between IMRT and proton radiation therapy. In this study, a planned secondary analysis will be performed, comparing the treatment and toxicity outcome between IMRT and proton. The data on the IMRT and proton comparison from this trial will be used to design future multi-center prospective trials and to determine if randomized trial is necessary.
In this study, the treatment technique employed for an individual case will not be determined by the treating physician(s), but rather by the most advanced technology available at the treating institution for the treatment of the sinonasal cancer. At the Massachusetts General Hospital (MGH), proton beam therapy will be used for patients who meet the eligibility criteria. For institutions where protons are not available or institutions where the proton planning systems have not been optimized, IMRT exclusively will be used for the treatment of sinonasal cancer. Patient and tumor characteristics are expected to be comparable between IMRT- and proton- institutions
|Condition or disease||Intervention/treatment||Phase|
|Adenoid Cystic Carcinoma Squamous Cell Carcinoma Sinonasal Carcinoma Sinonasal Undifferentiated Carcinoma Mucoepidermoid Carcinoma Schneiderian Carcinoma Myoepithelial Carcinoma Esthesioneuroblastoma Melanoma||Radiation: Proton radiation therapy Radiation: Intensity-modulated radiotherapy||Not Applicable|
Subjects will receive daily proton radiation treatment as outpatients at the Francis H. Burr Proton Center at Massachusetts General Hospital. The subjects may also receive concurrent standard chemotherapy every week during their radiation therapy. This chemotherapy is considered standard treatment for their cancer and is not being done for research purposes.
In addition to daily radiation treatments, subjects will have the following tests every week: review of side effects; physical exam, including weight, height, neurological exam and vital signs; and blood tests, only for those subjects also receiving chemotherapy.
Subjects will be followed for 5 years after the completion of study treatment. The first follow-up visit will be 6-8 weeks after completion of study treatment. Additional follow-up visits will be performed every 3 months during the first 2 years following completion of radiation then every 6 month during years 3-5. At each follow-up visit, subjects will receive a physical exam, chest CT scan (at 1st follow-up visit then at least every 6 months), a CT or MRI tumor assessment (at 1st follow-up visit then at least every 6 months), quality-of-life questionnaire, hearing test, neuro-ophthalmology test, and neurocognitive test.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||90 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Phase II Study of Intensity-Modulated or Proton Radiation Therapy for Locally Advanced Sinonasal Malignancy|
|Study Start Date :||July 2011|
|Estimated Primary Completion Date :||July 2021|
|Estimated Study Completion Date :||July 2024|
Active Comparator: Proton beam therapy
Subjects treated at Massachusetts General Hospital with proton beam therapy
Radiation: Proton radiation therapy
Daily proton radiation therapy
Active Comparator: IMRT
Intensity-modulated radiation therapy at institutions other than Massachusetts General Hospital
Radiation: Intensity-modulated radiotherapy
Daily intensity-modulated radiotherapy
Other Name: IMRT
- Local Control Rates [ Time Frame: 2 years ]To determine the local control rates with IMRT or proton radiation therapy at 2 years.
- Vision preservation [ Time Frame: 5 years ]To determine the late visual-orbital late effects of IMRT or proton beam
- Regional control [ Time Frame: 2 years ]To determine the regional control at 2 years after IMRT or proton
- Survival [ Time Frame: 5 years ]To determine the long-term survival at 5 years after IMRT or proton
- QOL [ Time Frame: 5 years ]To assess quality-of-life (QOL) outcomes after IMRT or proton
- Patterns of Tumor Relapse [ Time Frame: 5 years ]To determine the patterns of tumor relapse after IMRT or proton
- Local control [ Time Frame: 5 years ]To determine long-term local control after IMRT or proton
- Neurocognitive function [ Time Frame: 5 years ]To determine long-term neurocognitive function after IMRT or proton
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01586767
|Contact: Annie W Chan, MDfirstname.lastname@example.org|
|Contact: Elizabeth Weyman, BAemail@example.com|
|United States, Massachusetts|
|Massachusetts General Hospital||Recruiting|
|Boston, Massachusetts, United States, 02114|
|Principal Investigator: Annie W Chan, MD|
|United States, Minnesota|
|Mayo Clinic Rochester||Recruiting|
|Rochester, Minnesota, United States, 55905|
|Contact: Robert Foote, M.D. 507-284-3551 firstname.lastname@example.org|
|Principal Investigator:||Annie W Chan, MD||Massachusetts General Hospital|