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NCT Number: NCT06641791

Palliative Steroeotactic Body Radiotherapy vs Palliative Standard Radiotherapy in Patients With Advanced Head and Neck Cancer

This study is being done to answer the following question: Does stereotactic body radiation therapy (SBRT) provide better cancer control compared to standard radiation therapy (RT) for those with advanced head and neck cancer?

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Arthur J.E. Child Comprehensive Cancer Centre, Calgary, Alberta, Canada

Loading trial locations.

About this study

Stereotactic body radiation therapy, or SBRT, is a cancer treatment that more precisely delivers radiation to the tumour area with less radiation going to unaffected areas around the tumour. It uses fewer treatments of higher doses compared to standard radiation therapy.

This study is being done to find out if this approach is better than the usual approach for advanced head and neck cancer. The usual approach is defined as care most people get for advanced head and neck cancer.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histologically confirmed mucosal squamous cell carcinoma (SCC) of the head and neck arising from at least one of the following sites: oro/hypopharynx, oral cavity, supraglottic larynx, maxillary sinus, nasal cavity, or unknown primary
  • Stages TX or T0-T4/N0-N3
  • Must be considered unfit for curative intent RT as determined by the treating oncologist(s)
  • Geriatric 8 score <14
  • Patient must be ≥18 years of age
  • Staging CT or MRI of the head and neck within 8 weeks prior to randomization
  • Chest CT or x-ray. PET CT is permitted if CT is of diagnostic quality.
  • Eastern Cooperative Oncology Group (ECOG) Performance Status 0-3
  • Participants of childbearing potential must have agreed to use a highly effective contraceptive method during protocol therapy.
  • Patients with a prior malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational treatment are eligible for this trial.

Exclusion criteria

  • Patients with nasopharyngeal carcinoma.
  • Prior systemic therapy (including immunotherapy).
  • Prior radiotherapy to the head and neck excluding superficial radiotherapy for head and neck skin cancer that does not overlap with current protocol treatment.
  • Prior head and neck cancer excluding skin cancer.
  • Patients with tumour locations/at risk of SBRT toxicity, including glottic/subglottic larynx, T4 hypopharynx, post-cricoid, cervical esophagus, circumferential pharyngeal involvement, extension/proximity to brain/optic structures, any single tumour mass >8 cm (in one dimension).
  • > 2 nodal levels (Level 1a/b not counted); retropharyngeal lymph nodes (where the closest edge is < 2cm from the closest edge of CTV (primary or nodal) will not be considered as a different level). Note: a single lymph node mass that spans 2 levels will be considered as 1 level.
  • Gross tumour poorly visualized on CT/MRI.
  • Definitive radiological or clinically evident distant metastases.
  • Scleroderma/CREST syndrome.

Treatment and study plan

Standard Radiotherapy (SRT)

Radiation

2400 cGy in 3 fractions - day 0/7/21, OR, 2500 cGy in 5 fractions over 1 week

Stereotactic body radiotherapy (SBRT)

Radiation

4500 cGy in 5 fractions (twice a week to primary and nodal GTV, OR, 4000 cGy in 5 fractions twice a week if organs at risk.

Primary outcomes

  1. Overall Survival estimated according to Kaplan-Meier's methodology

    Time frame: 6 years

Secondary outcomes

  1. Progression-free Survival

    Time frame: 6 years

  2. Local Regional Failure Free Survival

    Time frame: 6 years

    defined as the time from the date of randomization to the date of any of the following, whichever comes first:

    • The first record of appearance (radiological or clinical) of local or regional disease progression/recurrence.
    • Surgery of primary tumour at any time performed for clinical or radiological (RECIST 1.1) disease persistence/progression/recurrence with tumour present/unknown on final pathology.
    • Neck dissection > 20 weeks from the end of radiation therapy performed for clinical or radiological (RECIST 1.1) disease persistence/progression/recurrence with tumour present/unknown on final pathology.
  3. Response Rate evaluated by RECIST

    Time frame: 6 years

  4. Number and Severity of Adverse Events

    Time frame: 6 years

  5. Patient Reported Outcomes utilizing PRO-CTCAE

    Time frame: 6 years

    We will qualitatively compare PRO-CTCAE item scores between arms at 8 weeks from the start of RT, and examine PRO-CTCAE item scores at 12 months post-RT in the SBRT arm, as an indicator or persisting (consequential or "late") RT toxicity with SBRT to the head and neck region.

  6. Patient Reported Outcomes utilizing FACT-HN

    Time frame: 6 years

    proportion of patients between arms who have a meaningful worsening (12 points or greater) of QOL

  7. Healthcare Resource Utilization utilizing EQ-5D-5L

    Time frame: 6 years

    All enrolled participants who have received at least one fraction of protocol therapy are evaluable for health economics. Those who have completed the Health Utilities Index (EQ-5D-5L), will be evaluable for cost-utility analyses.

Study contacts

Contact information is provided by the study sponsor or research team.

Wendy Parulekar

CONTACT

[email protected]

613-533-6430

Sponsors and collaborators

Lead sponsor

Canadian Cancer Trials Group

Network

Collaborators

  • Canadian Institutes of Health Research (CIHR)

Registry information

Official study title

A Phase III Randomized Controlled Trial Comparing Palliative Stereotactic Body Radiotherapy vs. Palliative Standard Radiotherapy in Patients With Advanced Head and Neck Cancer

Important dates

Study start
2025
Primary completion
2031
Study completion
2031
First posted
Oct 15, 2024
Registry last updated
Jul 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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