A Study of Adaptive Radiotherapy of Head-neck Cancer Using Daily Replanning and Optimization of the Treatment Plan.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorRigshospitalet, Denmark

About this trial

Radiotherapy of head-neck cancer is associated with significant side effects. Using daily online adaptive radiotherapy to account for the changing anatomy, radiation to organs at risk can be lowered. We will investigate whether this is feasible and associated with a reduction in the risk of toxicity.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with histologically proven squamous cell carcinoma of the pharynx or larynx planned for primary radiotherapy with curative intent No current or earlier malignancies, which may influence treatment, evaluation or outcome of the head-neck cancer Informed consent as required by law The patient cannot participate in conflicting protocols Stage I-IV (excluding T1-T2N0 carcinoma of the glottic larynx) ECOG/WHO performance status 0-2

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

  • Daily online adaptive radiotherapy

    Radiation

    The patients will undergo daily online adaptive re-optimisation of the radiotherapy treatment plan following daily recontouring.

Treatment groups

40 Participants
are divided into 1 treatment group
Group A: Daily online adaptive radiotherapy for head and neck cancerExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Risk of dysphagia and xerostomia six months post-treatment assesed by normal-tissue complication probability (NTCP) models

Time frame
6 months after treatment

Secondary outcomes

Other outcomes

Sponsors and contacts

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