Larynx CancerNCT00160095
Patient Selection for Hypoxia Modifying Treatments in Larynx Carcinomas
An observational study of Larynx Cancer, run by Radboud University Medical Center at 5 sites in Netherlands.
Trial summary
The purpose of this study is to identify in a prospective manner microregional profiles of oxygenation and proliferation based on exogenous and endogenous markers that are predictive for outcome of radiotherapy in squamous cell carcinoma of the larynx and to investigate if these profiles can identify patients that are… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Larynx Cancer
- How many people
- 79 participants
- Where
- 5 sitesNetherlands
- Study dates
- Jul 2001to Mar 2013
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Squamous cell carcinoma of the larynx
Who may be able to join
- Pathological confirmed squamous cell carcinoma of the larynx.
- TNM-classification (UICC 1997, appendix I):
- T3-4 glottic or supraglottic carcinoma
- T2 glottic carcinoma with impaired cord mobility or subglottic extension
- T2 supraglottic carcinoma with invasion of mucosa of base of tongue or vallecula or invasion of the medial wall of the piriform sinus.
- any N-stage, M0.
Show all 10Show fewer
- WHO performance status 0 or 1.
- Age > 18 years.
- Written informed consent.
- Treatment in the ARCON phase III trial
Who cannot join
- Prior or concurrent treatment for this tumour.
- Severe stridor and adequate debulking of airway not possible.
- Impaired renal function: serum creatinine above upper normal limit.
- Use of nephrotoxic medication (including ACE-inhibitors) that cannot be discontinued for the duration of the radiation treatment.
- Impaired hepatic function: ASAT and ALAT more than 1.5 times the upper normal limit.
- Use of anti-convulsants that cannot be discontinued for the duration of the radiation treatment.
- History of malignancy during the previous 5 years except basal cell carcinoma of skin, carcinoma in situ of the cervix, or superficial bladder neoplasm (pTa).
Trial locations and contacts
5 sites in 1 country.
5 sites in 1 country
Netherlands5 sites
Free University Medical Centre Amsterdam
Amsterdam, po 7057 1007 MB
Rijnstate Ziekenhuis Arnhem
Arnhem, po 9555 6800 TA
Academic Hospital Maastricht
Maastricht, po 5800 6202 AZ
Radboud University Nijmegen Medical Centre
Nijmegen, 6500 HB
Universitair Medisch Centrum Utrecht
Utrecht, po 85500 3508 GA
About this study
Official title: Patient Selection for Hypoxia Modifying Treatments Based on Functional Microregional Imaging of Tumor Vasculature, Oxygenation and Proliferation in Squamous Cell Carcinoma of the Larynx
The purpose of this study is to identify in a prospective manner microregional profiles of oxygenation and proliferation based on exogenous and endogenous markers that are predictive for outcome of radiotherapy in squamous cell carcinoma of the larynx and to investigate if these profiles can identify patients that are most likely to benefit from hypoxia modifying treatment strategies like ARCON (Accelerated radiotherapy combined with carbogen breathing and nicotinamide).
Read the detailed description
Purpose
Prognostic indicators discriminate patients with good and bad prognosis. Predictive assays are tools that select patients for specific treatments or treatment modifications such that outcome will be improved relative to conventional treatment. In oncology, many prognostic indicators based on clinical or biological tumor characteristics have been described but only very few have proven to be useful as predictive assays. We have developed an imaging modality for coregistration of tumor oxygenation and proliferation at the microregional level with preservation of the tumor anatomy and the microenvironmental structure. We have strong indications that this functional imaging can be a powerful tool for identifying those patients that will profit from hypoxia modifying treatments.
Tumor oxygenation and proliferation are recognized as important determinants of the outcome of radiotherapy and possibly also of other treatment modalities in a number of tumor types and in particular in squamous cell carcinomas. Various exogenous and endogenous markers for hypoxia and proliferation are currently available which can be studied in relation to each other, the tumor architecture and the tumor microenvironment using immunohistochemistry and advanced image analysis techniques.
The purpose of this project is to identify microregional profiles of oxygenation and proliferation based on exogenous and endogenous markers that:
- Are predictive for outcome of radiotherapy in squamous cell carcinoma of the larynx.
- Can identify the patients that are most likely to benefit from hypoxia modifying treatment strategies. And to:
- Validate these marker profiles in a prospective manner and in a sufficiently large group of patients.
Plan of investigation
In 2001 a multicenter randomized trial was initiated comparing accelerated radiotherapy with carbogen and nicotinamide as hypoxic modifiers against accelerated radiotherapy alone in patients with carcinoma of the larynx. This trial is approved and supported by the Dutch Cancer Society and currently 6 Dutch and 1 British center are participating. This trial provides a unique opportunity to prospectively test oxygenation and proliferation related marker profiles in a large homogeneous patient population and to assess the predictive capacity in a comparative setting with one group of patients receiving a hypoxia modifying treatment and the other group not.
Paraffin-embedded biopsy specimens will be collected from all patients entered in this trial. In part of the patients, biopsies will be taken after injection of the hypoxic marker pimonidazole and the S-phase marker iododeoxyuridine (IdUrd). Sections will be immunohistochemically processed and stained for various combinations of vascular markers, endogenous hypoxia and proliferation markers and, if applicable, for pimonidazole and IdUrd. The sections will be analyzed by computerized image processing. Apart from overall single parameter values that will be obtained, the interrelationship of the various parameters will be studied and the microregional phenotype of the tumors will be characterized by quantification and integration of the marker profiles. The information thus obtained will be related to treatment outcome in terms of both local control and survival and results from the two treatment groups will be compared.
Possible results
This investigation can identify oxygenation and proliferation related parameters and profiles that are predictive for outcome of radiotherapy in squamous cell carcinoma of the larynx and provide a selection tool for hypoxia modifying treatments. The principle of characterization of the tumor phenotype at the microregional level using functional imaging may also be applied to other tumor types and treatment strategies.
- Conditions
- Larynx Cancer
- Keywords
- larynx carcinoma, Tumor hypoxia, microregional imaging, hypoxia modifying treatment
- Medical subject headings
- Laryngeal Neoplasms
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Sep 2005 (estimated)
- Study startJul 2001
- Primary completionMar 2010
- Study completionMar 2013
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Larynx CancerStudies of the same condition, open and under way.
- More trials run by Radboud University Medical CenterThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 79 participants (actual)
Sponsor and investigators
- Lead sponsor
- Radboud University Medical Center
- Sponsor type
- University, hospital or other
- Collaborators
- Dutch Cancer Society
- Responsible party
- Sponsor
- Investigators
- Johannes HA Kaanders, M.D., Ph.D., Principal investigator, Radboud University Nijmegen Medical Centre, Dept Radiation Oncology
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00160095
- Sponsor's protocol ID
- 088
- Other IDs
- KUN 2003-2899
- Status last verified
- May 2015
- First submitted
- 9 Sep 2005
- Last updated
- 7 May 2015
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 7 May 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Patient Selection for Hypoxia Modifying Treatments Based on Functional Microregional Imaging of Tumor Vasculature, Oxygenation and Proliferation in Squamous Cell Carcinoma of the Larynx
- ClinicalTrials.gov ID
- NCT00160095
- Acronym / sponsor ID
- 088
- Conditions
- Larynx Cancer
- Keywords
- larynx carcinoma, Tumor hypoxia, microregional imaging, hypoxia modifying treatment
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 79 participants (actual)
- Lead sponsor
- Radboud University Medical CenterUniversity, hospital or other
- Collaborators
- Dutch Cancer Society
- Study start
- Jul 2001
- Primary completion
- Mar 2010 (actual)
- Study completion
- Mar 2013 (actual)
- First posted
- 12 Sep 2005 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to identify in a prospective manner microregional profiles of oxygenation and proliferation based on exogenous and endogenous markers that are predictive for outcome of radiotherapy in squamous cell carcinoma of the larynx and to investigate if these profiles can identify patients that are most likely to benefit from hypoxia modifying treatment strategies like ARCON (Accelerated radiotherapy combined with carbogen breathing and nicotinamide).
Detailed description
Purpose
Prognostic indicators discriminate patients with good and bad prognosis. Predictive assays are tools that select patients for specific treatments or treatment modifications such that outcome will be improved relative to conventional treatment. In oncology, many prognostic indicators based on clinical or biological tumor characteristics have been described but only very few have proven to be useful as predictive assays. We have developed an imaging modality for coregistration of tumor oxygenation and proliferation at the microregional level with preservation of the tumor anatomy and the microenvironmental structure. We have strong indications that this functional imaging can be a powerful tool for identifying those patients that will profit from hypoxia modifying treatments.
Tumor oxygenation and proliferation are recognized as important determinants of the outcome of radiotherapy and possibly also of other treatment modalities in a number of tumor types and in particular in squamous cell carcinomas. Various exogenous and endogenous markers for hypoxia and proliferation are currently available which can be studied in relation to each other, the tumor architecture and the tumor microenvironment using immunohistochemistry and advanced image analysis techniques.
The purpose of this project is to identify microregional profiles of oxygenation and proliferation based on exogenous and endogenous markers that:
- Are predictive for outcome of radiotherapy in squamous cell carcinoma of the larynx.
- Can identify the patients that are most likely to benefit from hypoxia modifying treatment strategies. And to:
- Validate these marker profiles in a prospective manner and in a sufficiently large group of patients.
Plan of investigation
In 2001 a multicenter randomized trial was initiated comparing accelerated radiotherapy with carbogen and nicotinamide as hypoxic modifiers against accelerated radiotherapy alone in patients with carcinoma of the larynx. This trial is approved and supported by the Dutch Cancer Society and currently 6 Dutch and 1 British center are participating. This trial provides a unique opportunity to prospectively test oxygenation and proliferation related marker profiles in a large homogeneous patient population and to assess the predictive capacity in a comparative setting with one group of patients receiving a hypoxia modifying treatment and the other group not.
Paraffin-embedded biopsy specimens will be collected from all patients entered in this trial. In part of the patients, biopsies will be taken after injection of the hypoxic marker pimonidazole and the S-phase marker iododeoxyuridine (IdUrd). Sections will be immunohistochemically processed and stained for various combinations of vascular markers, endogenous hypoxia and proliferation markers and, if applicable, for pimonidazole and IdUrd. The sections will be analyzed by computerized image processing. Apart from overall single parameter values that will be obtained, the interrelationship of the various parameters will be studied and the microregional phenotype of the tumors will be characterized by quantification and integration of the marker profiles. The information thus obtained will be related to treatment outcome in terms of both local control and survival and results from the two treatment groups will be compared.
Possible results
This investigation can identify oxygenation and proliferation related parameters and profiles that are predictive for outcome of radiotherapy in squamous cell carcinoma of the larynx and provide a selection tool for hypoxia modifying treatments. The principle of characterization of the tumor phenotype at the microregional level using functional imaging may also be applied to other tumor types and treatment strategies.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Squamous cell carcinoma of the larynx
Key inclusion criteria (10 listed)
- Pathological confirmed squamous cell carcinoma of the larynx.
- TNM-classification (UICC 1997, appendix I):
- T3-4 glottic or supraglottic carcinoma
- T2 glottic carcinoma with impaired cord mobility or subglottic extension
- T2 supraglottic carcinoma with invasion of mucosa of base of tongue or vallecula or invasion of the medial wall of the piriform sinus.
Key exclusion criteria (7 listed)
- Prior or concurrent treatment for this tumour.
- Severe stridor and adequate debulking of airway not possible.
- Impaired renal function: serum creatinine above upper normal limit.
- Use of nephrotoxic medication (including ACE-inhibitors) that cannot be discontinued for the duration of the radiation treatment.
- Impaired hepatic function: ASAT and ALAT more than 1.5 times the upper normal limit.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Not reported in the source record.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 7 May 2015.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Johannes HA Kaanders, M.D., Ph.D. principal investigator
Radboud University Nijmegen Medical Centre, Dept Radiation Oncology
5 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Larynx Cancer, run by Radboud University Medical Center at 5 sites in Netherlands.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 10 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 7 May 2015. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 5 sites in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 May 2015.