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Stereotactic Body Radiotherapy for Head and Neck Tumors

Nasopharyngeal Carcinoma Clinical Trial

Official title:
Phase IV Trial to Use Stereotactic Body Radiotherapy for Head and Neck Tumors

Clinical Trial Summary

This study will evaluate the local control rates as well as acute and late toxicity rates of stereotactic body radiotherapy (SBRT) for the treatment of benign and malignant head and neck tumors.

Clinical Trial Description

This single site, non-randomized, prospective, phase IV study includes 3 patient groups to be treated with SBRT:

- Benign tumors, such as paraganglioma, chordoma, chondrosarcoma, as the sole treatment or to gross residual disease after maximal safe resection

- Malignant tumors, such as nasopharynx cancer and squamous cell carcinoma, after initial external beam radiation (Residual Disease Group)

- Unresectable malignant tumors, such as nasopharynx cancer and squamous cell carcinoma, adenocarcinomas, and sarcomas which are recurrent after prior radiation (Primary RT Group) Data collected will include baseline patient demographics, pathology data, radiation therapy procedure, tumor recurrence data, and toxicities.

Follow up data will be collected during the patient's standard office visits. The anticipated duration of this study is 5 years. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01344356
Study type Interventional
Source Mercy Research
Contact
Status Completed
Phase Phase 4
Start date July 2008
Completion date May 2018
View Details
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