Trial of Stereotactic HYpofractionateD RadioAblative (HYDRA) Treatment of Laryngeal Cancer

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorM.D. Anderson Cancer Center

About this trial

To find the highest tolerable dose of stereotactic hypofractionated radioablation (HYDRA) radiation that can be given to patients with laryngeal cancer. The safety of this radiation will also be studied.

Eligibility criteria

Qualifiers

Patients older than 18 years of age with histologically proven squamous cell carcinoma of the larynx.

Stage T1N1/T2-4aN0-1 disease, as defined by American Joint Committee on Cancer (AJCC) criteria.

ECOG (Zubrod) performance status 0-2.

Must be functionally and technically fit for partial laryngectomy. Subsite study candidates will be evaluated by enrolling physician. The assessment checklist will be submitted at time of enrollment and evaluated by Dr. Gross or Dr. Phan.

Disqualifiers

Patients who have undergone resection of primary disease.

Patients who have received induction chemotherapy for their cancer diagnosis.

Patients who have undergone a diverting tracheostomy which is either a) traversing directly through tumor, b) has been placed for true airway insufficiency. Patients with a tracheostomy placed preemptively for impending airway compromise remain eligible for enrollment.

Prior cancer diagnosis, except appropriately treated localized epithelial skin cancer or cervical cancer.

Trial design

Treatments tested in this trial

  • Stereotactic Hypofractionated Radioablation
  • Questionnaires

Treatment groups

11 Participants
are divided into 1 treatment group

Sponsors and collaborators

M.D. Anderson Cancer Center

Lead sponsor

Cancer Prevention Research Institute of Texas

Collaborator