Stereotactic Radiosurgery in Patients With Head and Neck Region Tumours

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorMaria Sklodowska-Curie National Research Institute of Oncology

About this trial

The goal of this study is to evaluate the safety and efficacy of the stereotactic boost applied in patients with H\&N tumours.

Eligibility criteria

Qualifiers

Patients with squamous cell carcinoma (SCC) or adenoid cystic carcinoma (ACC) of the H&N region qualified for radical treatment with (definitive or adjuvant (adjuvant radiotherapy or radiochemotherapy in postoperative cases of R2 resection or early locoregional recurrence unsuitable for reoperation)) radiotherapy or radiochemotherapy.

Patients with other malignant tumours of the H&N region (sarcomas, neuroendocrine carcinomas, differentiated carcinomas, undifferentiated carcinomas, or basaloid carcinomas) qualified for radical treatment with (definitive or adjuvant (adjuvant radiotherapy or radiochemotherapy in postoperative cases of R2 resection or early locoregional recurrence unsuitable for reoperation)) radiotherapy or radiochemotherapy.

Patients with nonmalignant tumours of the H&N region (tumour mixtus or paraganglioma) demanding definitive or adjuvant radiotherapy.

Age: 18-80 years. Biomedicines 2022, 10, 1484 5 of 12

Disqualifiers

Do not meet the inclusion criteria.

Decompensated diabetes mellitus.

Myocardial infarction occurred up to 6 months before.

Pregnancy.

Trial design

Treatments tested in this trial

  • Stereotactic radiotherapy boost

Treatment groups

80 Participants
are divided into 1 treatment group