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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01427010
Other study ID # 2011/536
Secondary ID
Status Completed
Phase N/A
First received August 29, 2011
Last updated April 17, 2018
Start date January 2012
Est. completion date August 2015

Study information

Verified date April 2018
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Adaptive dose painting appears to increase the chance of cure at minimized radiation-induced toxicity in intensity-modulated radiotherapy (IMRT) for primary head and neck cancer. This could also be of importance in IMRT for recurrent and second primary head and neck cancers in previously irradiated territory.

This trial investigates the feasibility of continuous adaptive 18F-Fluorodeoxyglucose-Positron Emission Tomography-voxel ([18F]FDG-PET-voxel) intensity-based IMRT in reirradiation of patients with recurrent and second primary head and neck cancer.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date August 2015
Est. primary completion date August 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Histologically confirmed recurrences and second primary squamous cell carcinoma of the oral cavity, oropharynx, hypopharynx or larynx in the previously irradiated territory.

- Primary unresectable tumor and/or patients refused surgery.

- No grade 3 or more late toxicity (except xerostomia) after the initial radio(chemo)therapy for primary head and neck cancer.

- Minimal interval 12 months after the initial radio(chemo)therapy for primary head and neck cancer.

- Decision of a multidisciplinary tumor board on curative radiotherapy (in combination or not with targeted therapy with cetuximab)

- Karnofsky performance status =70%.

- Age = 18 years old.

- Informed consent obtained, signed and dated before specific protocol procedures.

Exclusion Criteria:

- Previous radiotherapy for cT1-2 cN0 M0 glottic cancer.

- Brachytherapy as treatment for second primary / recurrence.

- Distant metastases.

- Other second primary tumors that are not under control.

- Pregnant or lactating women.

- Elevated blood creatinine level.

- Allergy to the CT-contrast agents.

- Mental condition rendering the patient unable to understand the nature, scope, and possible consequences of the study.

- Patient unlikely to comply with protocol, i.e. uncooperative attitude, inability to return for follow-up visits, and unlikely to complete the study.

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
[18F]FDG-PET-voxel intensity-based IMRT
Non-controlled, non-randomized, prospective study on 18F-Fluorodeoxyglucose-Positron Emission Tomography ([18F]FDG-PET)-voxel intensity-based intensity-modulated radiotherapy (IMRT) (dose painting) adapted to the anatomical and biological changes as detected by per-treatment FDG-PET/Computertomography (CT) acquired at the end of the 2nd and the 4th week of treatment.

Locations

Country Name City State
Belgium Antwerp University Hospital Antwerp
Belgium University Hospital Ghent Ghent

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary To test success rate of continuous adaptive 18F-Fluorodeoxyglucose-Positron Emission Tomography ([18F]FDG-PET)-guided radiotherapy (intensity-modulated radiotherapy (IMRT) and/or helical tomotherapy). To test feasibility of continuous adaptive 18F-Fluorodeoxyglucose-Positron Emission Tomography ([18F]FDG-PET)-guided radiotherapy (intensity-modulated radiotherapy (IMRT) and/or helical tomotherapy) in treatment of recurrent and second primary head and neck cancer in the previously irradiated territory. 2 year
Secondary Estimation time to progression. At 6, 9 and 12 months
Secondary Evaluation tumor response. After 3 months.
Secondary Number of Participants with Adverse Events. Evaluation acute toxicity. Up to 3 months.

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