Skip to main content
OpenTrials
Active, Not Recruiting

NCT Number: NCT03070366

Stereotactic Radiotherapy Combined With Chemotherapy or Not for Treatment of Oligometastases in HNSCC

The aim of this study is to evaluate the rate of living patients at 1 year with a quality of life criteria (no decrease) and reduced toxicities. This criteria will be compared in both groups., A cost effectiveness study is scheduled also.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Notify Me

Key information

Age range

18 year–77 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Hôpital Nord Franche Comté

Montbéliard, 25209, France

About this study

Patients with cancers of aerodigestive tract have metastases limited in their evolution and a pauci-metastatic disease. In these cases, systemic therapy is the standard attitude. However, patients often received chemotherapy in their history and response rates are relatively low. The median survival is between 7 and 11 months with secondary effects and degradation of quality of life. It is a palliative treatment. Data on systemic treatment in the context of a micro-metastatic disease are limited. In contrast, stereotactic irradiation in pauci-metastatic context leads to better local control rates and may sustainedly reduce the progression of metastatic disease.

Stereotactic radiotherapy is increasing use in clinical practice for limited metastatic stages (oligo metastatic with 1-3 synchronized metastases). Radiotherapy in this indication has major advantages and a similar efficacy compared with other ablative treatments.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥ 18 years
  • PS:0-2
  • Estimated life expectancy ≥ 6 months
  • Histologically confirmed diagnosis of squamous cell carcinoma of the head and neck
  • Target metastases can be treated in stereotactic radiotherapy
  • 1-3 synchronized metastases with unrestricted anatomic site
  • Greater cumulative diameter of synchronous metastases in once organ (liver, lung or brain) ≤ 6 cm with GTV = Clinical Target Volume (CTV)
  • Global maximum diameter (GTV) allowed for pulmonary oligometastases (less than 2 cm from the mediastinum), brain, node, is ≤ 3cm
  • Implementation of a method for taking into account movements and uncertainties (IGRT) for limiting the margin of CTV to PTV (PTV) so as not to exceed 7 cm large cumulative diameter of PTV
  • Performing a positron emission tomography with 18F-2-fluoro-2-deoxy-D-glucose (FDG-PET) 4 weeks before the inclusion
  • In case of cerebral metastases, MRI diagnostic is required
  • If locoregional disease is treated, controlled and non-progressive for more than three months (+/- 4 weeks) at baseline, synchronized initial tumor is possible
  • If metachronous metastases, locoregional disease previously treated should be monitored and considered not progressive for more than three months at baseline
  • In case of prior cancer other than HNSCC, complete remission for over 5 years is possible, any biopsy of metastases is left to the appreciation of referring physician
  • No chemotherapy or local treatment of metastases in the previous 6 months
  • Laboratory tests consistent with the achievement of chemotherapy: Leukocytes> 3,000 / mm3 (including polynuclear> 2000 / mm3) platelets> 150,000 / mm3, serum glutamate oxaloacetate transminase (SGOT), serum glutamate pyruvate transaminase (SGPT), alkaline phosphatase, bilirubin <2.5 upper limit of normal (ULN)
  • Affiliation to an health insurance
  • Informed Consent Form signed

Exclusion criteria

  • Concomitant participation in other interventional clinical trial within 4 weeks before inclusion
  • Other prior ablative treatment of targets metastases (surgery, radio frequency) in the previous six months
  • metachronous primitive tumor (second cancer) uncontrolled.
  • contraindication to any systemic therapy (chemotherapy and / or targeted therapy)
  • Known hypersensitivity reaction to 5FU, cisplatin, carboplatin, platin or cetuximab
  • Active infection (infection requiring IV antibiotics), including active tuberculosis and known and declared human immunodeficiency virus (HIV)
  • Other malignancies within 5 years prior to randomization, with the exception of adequately treated basal skin cancer and carcinoma in situ of the cervix
  • Individual deprived of liberty by judicial or administrative decision, or under any kind of guardianship
  • Pregnant or breast feeding women. Every woman who has childbearing potential, must have a negative pregnancy test (serum or urine) within 14 days previous treatment. Patients (men or women) must use a reliable method of contraception throughout treatment and for at least 6 months after discontinuation of chemotherapy.

Treatment and study plan

Chemotherapy

Drug
  • cisplatin
  • 5FU
  • carboplatin
  • cetuximab

Stereotactic radiotherapy

Radiation

Stereotactic radiotherapy

Primary outcomes

  1. Overall Survival without quality of life deterioration

    Time frame: 1 year

    Overall Survival rate without definitive deterioration of quality of life (by QLQC30) measured at 1 year post treatment

Secondary outcomes

  1. Overall Survival

    Time frame: 1 year

  2. Progression free survival

    Time frame: through study completion, an average of 1 year

  3. Number of participants with adverse events grade 3 as assessed by CTCAE v4.0 within the first 6 months of treatment

    Time frame: up to 6 months

    Toxicity of grade > or equal to 3, occurring within the first 6 months of treatment

  4. Number of participants with treatment related adverse events as assessed by CTCAE v4.0

    Time frame: through study completion, an average of 1 year

  5. Overall response rate

    Time frame: through study completion, an average of 1 year

Sponsors and collaborators

Lead sponsor

Groupe Oncologie Radiotherapie Tete et Cou

Other

Registry information

Official study title

Randomized Phase II Trial Comparing Chemotherapy Combined With Stereotactic Radiotherapy and Stereotactic Radiotherapy Alone, for Treatment of Oligometastases in Squamous Cell Cancers of the Upper Aerodigestive Tract

Acronym: OMET

Important dates

Study start
2015
Primary completion
2026
Study completion
2026
First posted
Mar 3, 2017
Registry last updated
Sep 2, 2025

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.

Published trials that share one or more normalized conditions with this study.