A Study of Mucosal Sparing Proton Beam Therapy (PBT) in Resected Oropharyngeal Tumors

Mayo Clinic64 enrolled

Overview

This study is an observational study evaluating the clinical outcomes of mucosal sparing proton beam therapy (PBT) after resection of favorable risk oropharyngeal cancer patients. Subjects will be screened at outpatient clinic visit appointments and interested qualified subjects will be consented and offered participation in this study. Once consent has been obtained baseline adverse event and Quality of Life (QOL) data will be collected and subjects will undergo adjuvant PBT and follow-up at 3 months, 12 months, and 24 months. No study-specific visits or evaluations will be required. Patients will be evaluated according to the physician's standard practice and discretion. Patient data will be drawn from the patients' medical records and reported by means of a web-based electronic data collection (EDC) system. Patients will be considered "on study" until 24 months of observation has occurred, withdrawal of consent, lost to follow-up, or study closure.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Oropharyngeal Tumor

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Resection of oropharyngeal tumor by transoral surgery using frozen section margin analysis resulting in a negative margin resection * No extensive perineural invasion after review by head and neck pathologist * No lymphovascular invasion after review by head and neck pathologist * Pathologic stage T1-2 N1-3 M0 disease Exclusion Criteria: * T3 or T4 primary stage disease * Prior radiation therapy to the head and neck

Locations (2)

Outcomes

Primary Outcomes

Local Control Rate in Patients Treated with Proton Beam Therapy after Resection Using Transoral Surgery

Local control rate will be assessed by standard of care head and neck clinical examination during routine followup visits

Time frame: 24 months