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NCT Number: NCT02112344

A Study of Intensity-modulated Radiotherapy in Patients With Squamous Cell Carcinoma of Unknown Primary (SCCUP) of the Head and Neck

Squamous cell carcinoma of unknown primary (SCCUP) site metastatic to cervical lymph nodes at presentation is a relatively rare entity forming about 2% of all head and neck carcinomas.

Typically patients are treated with ipsilateral modified radical neck dissection (MRND) and post-operative radiotherapy (PORT) or chemoradiotherapy.

There is a lack of consensus on the radiotherapy target volumes that should be treated after neck dissection. The most common radiotherapy techniques are either unilateral cervical lymph node irradiation to achieve local control in the ipsilateral neck or TMI of the head and neck region with the aim of eradicating the primary and the microscopic neck disease.

Treatment of the ipsilateral hemi-neck alone is of low toxicity and may achieve local control in the cervical nodes. Potential occult primary sites in the head and neck mucosa, and any sub-clinical metastatic disease in the contralateral side of the neck are left untreated. If a primary tumour subsequently becomes apparent the previous radiotherapy may make further radiotherapy difficult to deliver.

Some groups recommend bilateral neck and total mucosal irradiation in this setting claiming improved local control. With conventional radiotherapy technique this is at the price of significant acute toxicity and chronic morbidity, mainly xerostomia with its associated complications and effects on quality of life (QOL).

Intensity modulated radiotherapy (IMRT) has been shown to reduce the dose to salivary gland tissue and consequently may reduce the incidence of xerostomia and improve quality of life (QOL) in head and neck cancer patients.

An analysis of parotid-sparing IMRT at the University of Michigan established a mean dose threshold for both stimulated (26 Gy), and unstimulated (24 Gy) saliva flow rates. For the same end-point (less than 25% of flow at baseline one year post radiation) Roesink et al established a TD50 of 39 Gy.

The investigators performed a planning study to assess the feasibility of IMRT to spare the parotid gland while delivering bilateral neck and TMI. The mean dose to the contralateral parotid gland using IMRT was below the threshold of 24 Gy for unstimulated salivary flow, predicting a fairly low risk of radiation induced xerostomia. The mean dose to the ipsilateral parotid gland was 32 Gy which was below the TD50 dose based on the Roesink data.

This study assesses the safety and tolerability of delivering IMRT in clinical practice to treat patients with SCCUP of the head and neck region, who require bilateral neck and pan-mucosal irradiation.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Squamous cell carcinomas metastatic to cervical lymph node with occult primary requiring bilateral neck and pan mucosal irradiation.
  • Radiotherapy either as primary therapy or post-operative (adjuvant irradiation).
  • Neoadjuvant and concomitant chemotherapy are permitted.
  • All patients must be suitable to attend regular follow-up and undergo toxicity assessment.
  • Stage T0, N1-3, M0 disease
  • WHO Performance Status 0-1.
  • Patient should have a negative PET/CT scan for a primary tumour.

Exclusion criteria

  • Previous radiotherapy to the head and neck region
  • Previous malignancy except non-melanoma skin cancer
  • Previous or concurrent illness which in the investigators opinion would interfere with either completion of therapy or follow-up
  • Prophylactic use of amifostine or pilocarpine is not allowed
  • Brachytherapy is not allowed as part of the treatment

Treatment and study plan

IMRT

Radiation

Primary outcomes

  1. Feasibility of delivering IMRT

    Time frame: 7 weeks after starting radiotherapy

    Feasibility of delivering IMRT in this setting i.e. all the patients completing the radiotherapy protocol without treatment breaks due to toxicity.

Secondary outcomes

  1. Incidence of acute dermatitis

    Time frame: 3 months after RT

    Outcome measured at baseline, weeks 1-6 during RT. Weeks 1-4 and 8 after RT.

  2. Incidence of >grade 1 late xerostomia

    Time frame: 5 years

    Outcome measured at 3, 6, 12, 18, 24 months after RT.

  3. Number of patients who do not relapse at the local site

    Time frame: 5 years

    Local control assessed at 3, 6 months, then every 6 months to 5 years.

  4. Overall survival

    Time frame: 5 years

    Assessed at 3 and 6 months then every 6 months to 5 years.

  5. Incidence of acute alopecia

    Time frame: 3 months after RT

    Outcome measured at baseline, weeks 1-6 during RT. Weeks 1-4 and 8 after RT.

  6. Incidence of >grade 1 acute dysphagia

    Time frame: 3 months after RT

    Outcome measured at baseline, weeks 1-6 during RT. Weeks 1-4 and 8 after RT.

  7. Incidence of > grade 1 acute mucositis

    Time frame: 3 months after RT

    Outcome measured at baseline, weeks 1-6 during RT. Weeks 1-4 and 8 after RT.

  8. Incidence of acute radiation induced pain

    Time frame: 3 months after RT

    Outcome measured at baseline, weeks 1-6 during RT. Weeks 1-4 and 8 after RT.

  9. Incidence of >grade 1 acute xerostomia

    Time frame: 3 months after RT

    Outcome measured at baseline, weeks 1-6 during RT. Weeks 1-4 and 8 after RT.

  10. Incidence of acute radiation induced fatigue

    Time frame: 3 months after RT

    Outcome measured at baseline, weeks 1-6 during RT. Weeks 1-4 and 8 after RT.

  11. Incidence of > grade 1 late dysphagia

    Time frame: 5 years after RT

    Outcome measured at 3, 6, 12, 18, 24 months after RT.

  12. Incidence of late oesophageal stricture

    Time frame: 5 years after RT

    Outcome measured at 3, 6, 12, 18, 24 months after RT.

  13. Incidence of >grade 1 late hoarse voice

    Time frame: 5 years after RT

    Outcome measured at 3, 6, 12, 18, 24 months after RT.

  14. Incidence of late radiation induced neurological dysfunction

    Time frame: 5 years

    Outcome measured at 3, 6, 12, 18, 24 months after RT.

  15. Incidence of >grade1 late skin toxicity

    Time frame: 5 years after RT

    Outcome measured at 3, 6, 12, 18, 24 months after RT.

Sponsors and collaborators

Lead sponsor

Royal Marsden NHS Foundation Trust

Other

Registry information

Official study title

A Phase I Study of Intensity-modulated Radiotherapy in Patients With Squamous Cell Carcinoma of Unknown Primary (SCCUP) of the Head and Neck

Important dates

Study start
2007
Primary completion
2010
Study completion
2015
First posted
Apr 11, 2014
Registry last updated
Sep 7, 2020

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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